16. Literaturverzeichnis – Actinic keratosis and squamous cell carcinoma of the skin
1. Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF), S3-Leitlinie Prävention von Hautkrebs, Langversion 2.1, 2021. AWMF Registernummer: 032/052OL:
2. Schafer, I., Reusch, M., Siebert, J., Spehr, C., Augustin, M., Health care characteristics of basal cell carcinoma in Germany: the role of insurance status and socio-demographic factors, J.Dtsch.Dermatol.Ges., 2014. 12(9): p. 803-811., https://www.ncbi.nlm.nih.gov/pubmed/25176460
3. Flohil, S. C., van der Leest, R. J., Dowlatshahi, E. A., Hofman, A., de Vries, E., Nijsten, T., Prevalence of actinic keratosis and its risk factors in the general population: the Rotterdam Study, J Invest Dermatol, 2013. 133(8): p. 1971-8., https://pubmed.ncbi.nlm.nih.gov/23510990/
4. Green, A. C., Epidemiology of actinic keratoses, Curr Probl Dermatol, 2015. 46: p. 1-7., https://www.ncbi.nlm.nih.gov/pubmed/25561199
5. Memon, A. A., Tomenson, J. A., Bothwell, J., Friedmann, P. S., Prevalence of solar damage and actinic keratosis in a Merseyside population, Br J Dermatol, 2000. 142(6): p. 1154-9., https://www.ncbi.nlm.nih.gov/pubmed/10848739
6. Schmitt, J., Seidler, A., Diepgen, T. L., Bauer, A., Occupational ultraviolet light exposure increases the risk for the development of cutaneous squamous cell carcinoma: a systematic review and meta-analysis, Br.J.Dermatol., 2011. 164(2): p. 291-307., https://www.ncbi.nlm.nih.gov/pubmed/21054335
7. Leiter, U., Keim, U., Eigentler, T., Katalinic, A., Holleczek, B., Martus, P., et.al. Incidence, Mortality, and Trends of Nonmelanoma Skin Cancer in Germany, J Invest Dermatol, 2017., https://www.ncbi.nlm.nih.gov/pubmed/28487088
8. Katalinic, A., Kunze, U., Schafer, T., Epidemiology of cutaneous melanoma and non-melanoma skin cancer in Schleswig-Holstein, Germany: incidence, clinical subtypes, tumour stages and localization (epidemiology of skin cancer), Br.J.Dermatol., 2003. 149(6): p. 1200-1206., https://www.ncbi.nlm.nih.gov/pubmed/14674897
9. Leiter, U., Garbe, C., Epidemiology of melanoma and nonmelanoma skin cancer--the role of sunlight, Adv.Exp.Med.Biol, 2008. 624: p. 89-103., https://pubmed.ncbi.nlm.nih.gov/18348450/
10. Rudolph, C., Schnoor, M., Eisemann, N., Katalinic, A., Incidence trends of nonmelanoma skin cancer in Germany from 1998 to 2010, J.Dtsch.Dermatol.Ges., 2015. 13(8): p. 788-797., https://pubmed.ncbi.nlm.nih.gov/26213814/
11. Eisemann, N., Jansen, L., Castro, F. A., Chen, T., Eberle, A., Nennecke, A., et.al. Survival from non-melanoma skin cancer in Germany, Br.J.Dermatol., 2015., https://pubmed.ncbi.nlm.nih.gov/26676514/
12. Waldmann, A., Nolte, S., Weinstock, M. A., Breitbart, E. W., Eisemann, N., Geller, A. C., et.al. Skin cancer screening participation and impact on melanoma incidence in Germany--an observational study on incidence trends in regions with and without population-based screening, Br.J.Cancer, 2012. 106(5): p. 970-974., https://pubmed.ncbi.nlm.nih.gov/22294187/
13. Augustin, M., Stadler, R., Reusch, M., Schafer, I., Kornek, T., Luger, T., Skin cancer screening in Germany - perception by the public, J Dtsch Dermatol Ges, 2012. 10(1): p. 42-9., https://pubmed.ncbi.nlm.nih.gov/21923730/
14. Stang, A., Jockel, K. H., Declining mortality rates for nonmelanoma skin cancers in West Germany, 1968-99, Br.J.Dermatol., 2004. 150(3): p. 517-522., https://pubmed.ncbi.nlm.nih.gov/15030336/
15. Keim, U., van der Pols, J. C., Williams, G. M., Green, A. C., Exclusive development of a single type of keratinocyte skin cancer: evidence from an Australian population-based cohort study, J Invest Dermatol, 2015. 135(3): p. 728-33., https://www.ncbi.nlm.nih.gov/pubmed/25233075
16. Hollestein, L. M., de Vries, E., Nijsten, T., Trends of cutaneous squamous cell carcinoma in the Netherlands: Increased incidence rates, but stable relative survival and mortality 1989-2008, Eur.J.Cancer, 2012. 48(13): p. 2046-2053., https://pubmed.ncbi.nlm.nih.gov/22342554/
17. Xiang, F., Lucas, R., Hales, S., Neale, R., Incidence of nonmelanoma skin cancer in relation to ambient UV radiation in white populations, 1978-2012: empirical relationships, JAMA Dermatol., 2014. 150(10): p. 1063-1071., https://pubmed.ncbi.nlm.nih.gov/25103031/
18. Raasch, B. A., Buettner, P. G., Multiple nonmelanoma skin cancer in an exposed Australian population, Int.J.Dermatol., 2002. 41(10): p. 652-658., https://pubmed.ncbi.nlm.nih.gov/12390187/
19. Karia, P. S., Han, J., Schmults, C. D., Cutaneous squamous cell carcinoma: estimated incidence of disease, nodal metastasis, and deaths from disease in the United States, 2012, J.Am.Acad.Dermatol., 2013. 68(6): p. 957-966., https://pubmed.ncbi.nlm.nih.gov/23375456/
20. Brantsch, K. D., Meisner, C., Schonfisch, B., Trilling, B., Wehner-Caroli, J., Rocken, M., et.al. Analysis of risk factors determining prognosis of cutaneous squamous-cell carcinoma: a prospective study, Lancet Oncol, 2008. 9(8): p. 713-20., https://pubmed.ncbi.nlm.nih.gov/18617440/
21. Eigentler, TK, Leiter, U, Häfner, HM, Garbe, C, Röcken, M, Breuninger, H, Survival of Patients with Cutaneous Squamous Cell Carcinoma: Results of a Prospective Cohort Study., J Invest Dermatol, 2017. 137 (11)(11): p. 2309-2315., https://pubmed.ncbi.nlm.nih.gov/28736229/
22. Lewis, K. G., Weinstock, M. A., Trends in nonmelanoma skin cancer mortality rates in the United States, 1969 through 2000, J.Invest Dermatol., 2007. 127(10): p. 2323-2327., https://pubmed.ncbi.nlm.nih.gov/17522705/
23. Strunk, T., Szeimies, R. M., [Actinic keratoses. Pathogenesis, clinical aspect and modern therapeutic options], Hautarzt, 2014. 65(3): p. 241-52; quiz 253-4.
24. Marinescu, A., Stepan, A. E., Margaritescu, C., Marinescu, A. M., Zavoi, R. E., Simionescu, C. E., et.al. P53, p16 and Ki67 immunoexpression in cutaneous squamous cell carcinoma and its precursor lesions, Rom J Morphol Embryol, 2016. 57(2 Suppl): p. 691-696., https://www.ncbi.nlm.nih.gov/pubmed/27833960
25. El Ghissassi, F, Baan, R, Straif, K, Grosse, Y, Secretan, B, Bouvard, V, et.al. A review of human carcinogens--part D: radiation., Lancet Oncol, 2009. 10 (8)(8): p. 751-2., https://pubmed.ncbi.nlm.nih.gov/19655431/
26. Berg, D., Otley, C. C., Skin cancer in organ transplant recipients: Epidemiology, pathogenesis, and management, J Am Acad Dermatol, 2002. 47(1): p. 1-17; quiz 18-20., http://www.ncbi.nlm.nih.gov/pubmed/12077575
27. Euvrard, S., Kanitakis, J., Claudy, A., Skin cancers after organ transplantation, N Engl J Med, 2003. 348(17): p. 1681-91., http://www.ncbi.nlm.nih.gov/pubmed/12711744
28. Zwald, F. O., Brown, M., Skin cancer in solid organ transplant recipients: advances in therapy and management: part I. Epidemiology of skin cancer in solid organ transplant recipients, J Am Acad Dermatol, 2011. 65(2): p. 253-61; quiz 262., http://www.ncbi.nlm.nih.gov/pubmed/21763561
29. Ulrich, C., Schmook, T., Nindl, I., Meyer, T., Sterry, W., Stockfleth, E., Cutaneous precancers in organ transplant recipients: an old enemy in a new surrounding, Br.J.Dermatol., 2003. 149 Suppl 66: p. 40-42., https://www.ncbi.nlm.nih.gov/pubmed/14616348
30. Harwood, CA, Mesher, D, McGregor, JM, Mitchell, L, Leedham-Green, M, Raftery, M, et.al. A surveillance model for skin cancer in organ transplant recipients: a 22-year prospective study in an ethnically diverse population., Am J Transplant, 2013. 13 (1)(1): p. 119-29., https://pubmed.ncbi.nlm.nih.gov/23072567/
31. Marcil, I., Stern, R. S., Risk of developing a subsequent nonmelanoma skin cancer in patients with a history of nonmelanoma skin cancer: a critical review of the literature and meta-analysis, Arch Dermatol, 2000. 136(12): p. 1524-30., http://www.ncbi.nlm.nih.gov/pubmed/11115165
32. Lott, D. G., Manz, R., Koch, C., Lorenz, R. R., Aggressive behavior of nonmelanotic skin cancers in solid organ transplant recipients, Transplantation, 2010. 90(6): p. 683-7., http://www.ncbi.nlm.nih.gov/pubmed/20808266
33. Thompson, A. K., Kelley, B. F., Prokop, L. J., Murad, M. H., Baum, C. L., Risk Factors for Cutaneous Squamous Cell Carcinoma Recurrence, Metastasis, and Disease-Specific Death: A Systematic Review and Meta-analysis, JAMA Dermatol, 2016. 152(4): p. 419-28., https://www.ncbi.nlm.nih.gov/pubmed/26762219
34. Werner, R. N., Sammain, A., Erdmann, R., Hartmann, V., Stockfleth, E., Nast, A., The natural history of actinic keratosis: a systematic review, Br J Dermatol, 2013. 169(3): p. 502-18., https://www.ncbi.nlm.nih.gov/pubmed/23647091
35. Madani, S, Marwaha, S, Dusendang, JR, Alexeeff, S, Pham, N, Chen, EH, et.al. Ten-Year Follow-up of Persons With Sun-Damaged Skin Associated With Subsequent Development of Cutaneous Squamous Cell Carcinoma., JAMA Dermatol, 2021. 157 (5)(5): p. 559-565., https://pubmed.ncbi.nlm.nih.gov/33760003/
36. Schmitz, L, Brehmer, A, Falkenberg, C, Gambichler, T, Heppt, MV, Steeb, T, et.al. Treatment-resistant actinic keratoses are characterized by distinct clinical and histological features., Ital J Dermatol Venerol, 2021. 156 (2)(2): p. 213-219., https://pubmed.ncbi.nlm.nih.gov/33960752/
37. Schmitz, L, Kahl, P, Majores, M, Bierhoff, E, Stockfleth, E, Dirschka, T, Actinic keratosis: correlation between clinical and histological classification systems., J Eur Acad Dermatol Venereol, 2016. 30 (8)(8): p. 1303-7., https://pubmed.ncbi.nlm.nih.gov/26955898/
38. Fernandez-Figueras, M. T., Carrato, C., Saenz, X., Puig, L., Musulen, E., Ferrandiz, C., et.al. Actinic keratosis with atypical basal cells (AK I) is the most common lesion associated with invasive squamous cell carcinoma of the skin, Journal of the European Academy of Dermatology and Venereology : JEADV, 2015. 29(5): p. 991-7., http://onlinelibrary.wiley.com/doi/10.1111/jdv.12848/abstract
39. Ianhez, M, Fleury Junior, LF, Bagatin, E, Miot, HA, The reliability of counting actinic keratosis., Arch Dermatol Res, 2013. 305 (9)(9): p. 841-4., https://pubmed.ncbi.nlm.nih.gov/24045957/
40. Jiyad, Z, O'Rourke, P, Soyer, HP, Green, AC, Assessing the Concordance of Actinic Keratosis Counts on Digital Photographs with Clinical Examination in Organ Transplant Recipients., Acta Derm Venereol, 2017. 97 (3)(3): p. 351-353., https://pubmed.ncbi.nlm.nih.gov/27701669/
41. Sinnya, S, O'Rourke, P, Ballard, E, Tan, JM, Morze, C, Sahebian, A, et.al. Counting actinic keratosis - is photographic assessment a reliable alternative to physical examination in clinical trials?, Acta Derm Venereol, 2015. 95 (5)(5): p. 604-5., https://pubmed.ncbi.nlm.nih.gov/25572587/
42. Ratushny, V., Gober, M. D., Hick, R., Ridky, T. W., Seykora, J. T., From keratinocyte to cancer: the pathogenesis and modeling of cutaneous squamous cell carcinoma, The Journal of clinical investigation, 2012. 122(2): p. 464-72., http://www.ncbi.nlm.nih.gov/pubmed/22293185
43. Stockfleth, E., Ferrandiz, C., Grob, J. J., Leigh, I., Pehamberger, H., Kerl, H., Development of a treatment algorithm for actinic keratoses: a European Consensus, European journal of dermatology : EJD, 2008. 18(6): p. 651-9., http://www.ncbi.nlm.nih.gov/pubmed/18955209
44. Criscione, V. D., Weinstock, M. A., Naylor, M. F., Luque, C., Eide, M. J., Bingham, S. F., Actinic keratoses: Natural history and risk of malignant transformation in the Veterans Affairs Topical Tretinoin Chemoprevention Trial, Cancer, 2009. 115(11): p. 2523-30., http://www.ncbi.nlm.nih.gov/pubmed/19382202
45. Fuchs, A., Marmur, E., The kinetics of skin cancer: progression of actinic keratosis to squamous cell carcinoma, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 2007. 33(9): p. 1099-101., http://onlinelibrary.wiley.com/doi/10.1111/j.1524-4725.2007.33224.x/abstract
46. Heerfordt, I. M., Nissen, C. V., Poulsen, T., Philipsen, P. A., Wulf, H. C., Thickness of Actinic Keratosis Does Not Predict Dysplasia Severity or P53 Expression, Scientific reports, 2016. 6: p. 33952., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037398/pdf/srep33952.pdf
47. Jiyad, Z., O'Rourke, P., Soyer, H. P., Green, A. C., Actinic keratosis-related signs predictive of squamous cell carcinoma in renal transplant recipients: a nested case-control study, The British journal of dermatology, 2017. 176(4): p. 965-970., http://www.ncbi.nlm.nih.gov/pubmed/27584866
48. Pandey, S., Mercer, S. E., Dallas, K., Emanuel, P. O., Goldenberg, G., Evaluation of the prognostic significance of follicular extension in actinic keratoses, The Journal of clinical and aesthetic dermatology, 2012. 5(4): p. 25-8., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366442/pdf/jcad_5_4_25.pdf
49. Vilcea, A. M., Vilcea, I. D., Georgescu, C. V., Patrascu, V., The value of the histopathologic examination in the diagnosis and management of the actinic keratosis, Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie, 2012. 53(4): p. 927-34., http://www.ncbi.nlm.nih.gov/pubmed/23303015
50. Wallingford, S. C., Russell, S. A., Vail, A., Proby, C. M., Lear, J. T., Green, A. C., Actinic keratoses, actinic field change and associations with squamous cell carcinoma in renal transplant recipients in Manchester, UK, Acta dermato-venereologica, 2015. 95(7): p. 830-4., https://www.ncbi.nlm.nih.gov/pubmed/25784002
51. Smit, P., Plomp, E., Neumann, H. A., Thio, H. B., The influence of the location of the lesion on the absolute risk of the development of skin cancer in a patient with actinic keratosis, Journal of the European Academy of Dermatology and Venereology : JEADV, 2013. 27(6): p. 667-71., http://onlinelibrary.wiley.com/doi/10.1111/jdv.12008/abstract
52. Dirschka, T, Pellacani, G, Micali, G, Malvehy, J, Stratigos, AJ, Casari, A, et.al. A proposed scoring system for assessing the severity of actinic keratosis on the head: actinic keratosis area and severity index., J Eur Acad Dermatol Venereol, 2017. 31 (8)(8): p. 1295-1302., https://pubmed.ncbi.nlm.nih.gov/28401585/
53. Dreno, B., Cerio, R., Dirschka, T., Nart, I. F., Lear, J. T., Peris, K., et.al. A Novel Actinic Keratosis Field Assessment Scale for Grading Actinic Keratosis Disease Severity, Acta dermato-venereologica, 2017. 97(9): p. 1108-1113., http://www.ncbi.nlm.nih.gov/pubmed/28536731
54. Brinkman, J. N., Hajder, E., van der Holt, B., Den Bakker, M. A., Hovius, S. E., Mureau, M. A., The Effect of Differentiation Grade of Cutaneous Squamous Cell Carcinoma on Excision Margins, Local Recurrence, Metastasis, and Patient Survival: A Retrospective Follow-Up Study, Ann Plast Surg, 2015. 75(3): p. 323-6., https://pubmed.ncbi.nlm.nih.gov/24401812/
55. Campoli, M., Brodland, D. G., Zitelli, J., A prospective evaluation of the clinical, histologic, and therapeutic variables associated with incidental perineural invasion in cutaneous squamous cell carcinoma, J Am Acad Dermatol, 2014. 70(4): p. 630-6., https://www.ncbi.nlm.nih.gov/pubmed/24433872
56. Haisma, M. S., Plaat, B. E., Bijl, H. P., Roodenburg, J. L., Diercks, G. F., Romeijn, T. R., et.al. Multivariate analysis of potential risk factors for lymph node metastasis in patients with cutaneous squamous cell carcinoma of the head and neck, J Am Acad Dermatol, 2016. 75(4): p. 722-30., https://www.ncbi.nlm.nih.gov/pubmed/27473455
57. Cherpelis, B. S., Marcusen, C., Lang, P. G., Prognostic factors for metastasis in squamous cell carcinoma of the skin, Dermatol Surg, 2002. 28(3): p. 268-73., https://www.ncbi.nlm.nih.gov/pubmed/11896781
58. Ch'ng, S., Maitra, A., Allison, R. S., Chaplin, J. M., Gregor, R. T., Lea, R., et.al. Parotid and cervical nodal status predict prognosis for patients with head and neck metastatic cutaneous squamous cell carcinoma, J Surg Oncol, 2008. 98(2): p. 101-5., https://www.ncbi.nlm.nih.gov/pubmed/18523982
59. Ch'ng, S., Clark, J. R., Brunner, M., Palme, C. E., Morgan, G. J., Veness, M. J., Relevance of the primary lesion in the prognosis of metastatic cutaneous squamous cell carcinoma, Head Neck, 2013. 35(2): p. 190-4., https://www.ncbi.nlm.nih.gov/pubmed/22422542
60. Oddone, N., Morgan, G. J., Palme, C. E., Perera, L., Shannon, J., Wong, E., et.al. Metastatic cutaneous squamous cell carcinoma of the head and neck: the Immunosuppression, Treatment, Extranodal spread, and Margin status (ITEM) prognostic score to predict outcome and the need to improve survival, Cancer, 2009. 115(9): p. 1883-91., https://www.ncbi.nlm.nih.gov/pubmed/19224549
61. Petter, G., Haustein, U. F., [Histological and clinical prognostic factors in squamous cell carcinoma of the skin. A contribution to the multicenter carcinoma study of the association of surgical and oncological dermatology], Hautarzt, 1999. 50(6): p. 412-7., https://www.ncbi.nlm.nih.gov/pubmed/10427509
62. Roozeboom, M. H., Lohman, B. G., Westers-Attema, A., Nelemans, P. J., Botterweck, A. A., van Marion, A. M., et.al. Clinical and histological prognostic factors for local recurrence and metastasis of cutaneous squamous cell carcinoma: analysis of a defined population, Acta Derm Venereol, 2013. 93(4): p. 417-21., https://www.ncbi.nlm.nih.gov/pubmed/23138613
63. Schmults, C. D., Karia, P. S., Carter, J. B., Han, J., Qureshi, A. A., Factors predictive of recurrence and death from cutaneous squamous cell carcinoma: a 10-year, single-institution cohort study, JAMA Dermatol, 2013. 149(5): p. 541-7., https://www.ncbi.nlm.nih.gov/pubmed/23677079
64. Wermker, K., Kluwig, J., Schipmann, S., Klein, M., Schulze, H. J., Hallermann, C., Prediction score for lymph node metastasis from cutaneous squamous cell carcinoma of the external ear, Eur J Surg Oncol, 2015. 41(1): p. 128-35., https://www.ncbi.nlm.nih.gov/pubmed/25182221
65. Manyam, B. V., Garsa, A. A., Chin, R. I., Reddy, C. A., Gastman, B., Thorstad, W., et.al. A multi-institutional comparison of outcomes of immunosuppressed and immunocompetent patients treated with surgery and radiation therapy for cutaneous squamous cell carcinoma of the head and neck, Cancer, 2017. 123(11): p. 2054-2060., https://pubmed.ncbi.nlm.nih.gov/28171708/
66. Manyam, B. V., Gastman, B., Zhang, A. Y., Reddy, C. A., Burkey, B. B., Scharpf, J., et.al. Inferior outcomes in immunosuppressed patients with high-risk cutaneous squamous cell carcinoma of the head and neck treated with surgery and radiation therapy, J Am Acad Dermatol, 2015. 73(2): p. 221-7., https://www.ncbi.nlm.nih.gov/pubmed/26028524
67. Schmitz, L, Gupta, G, Stücker, M, Doerler, M, Gambichler, T, Welzel, J, et.al. Evaluation of two histological classifications for actinic keratoses - PRO classification scored highest inter-rater reliability., J Eur Acad Dermatol Venereol, 2019. 33 (6)(6): p. 1092-1097., https://pubmed.ncbi.nlm.nih.gov/30887613/
68. Schmitz, L, Gambichler, T, Gupta, G, Stücker, M, Stockfleth, E, Szeimies, RM, et.al. Actinic keratoses show variable histological basal growth patterns - a proposed classification adjustment., J Eur Acad Dermatol Venereol, 2018. 32 (5)(5): p. 745-751., https://pubmed.ncbi.nlm.nih.gov/28796914/
69. Schmitz, L, Gambichler, T, Kost, C, Gupta, G, Stücker, M, Stockfleth, E, et.al. Cutaneous squamous cell carcinomas are associated with basal proliferating actinic keratoses., Br J Dermatol, 2019. 180 (4)(4): p. 916-921., https://pubmed.ncbi.nlm.nih.gov/29526028/
70. Lee, DY, Kim, BR, Yang, S, Kim, M, Yoon, TY, Youn, SW, Histopathological predictor of the progression from actinic keratosis to squamous cell carcinoma: quantitative computer-aided image analysis., J Eur Acad Dermatol Venereol, 2021. 35 (1)(1): p. 116-122., https://pubmed.ncbi.nlm.nih.gov/32455470/
71. Conforti, C, Giuffrida, R, Pizzichetta, MA, Di Meo, N, Magaton-Rizzi, G, Zalaudek, I, Integrating the concept of field cancerization in the classification and risk assessment of cutaneous squamous cell carcinoma: proposal for a new classification and terminology of keratinocyte skin cancer., J Eur Acad Dermatol Venereol, 2019. 33 (9)(9): p. e327-e330., https://pubmed.ncbi.nlm.nih.gov/30980765/
72. Slaughter, D. P., Southwick, H. W., Smejkal, W., Field cancerization in oral stratified squamous epithelium; clinical implications of multicentric origin, Cancer, 1953. 6(5): p. 963-8., https://www.ncbi.nlm.nih.gov/pubmed/13094644
73. Braakhuis, B. J., Tabor, M. P., Kummer, J. A., Leemans, C. R., Brakenhoff, R. H., A genetic explanation of Slaughter's concept of field cancerization: evidence and clinical implications, Cancer Res, 2003. 63(8): p. 1727-30., https://www.ncbi.nlm.nih.gov/pubmed/12702551
74. Malvehy, J., A new vision of actinic keratosis beyond visible clinical lesions, J Eur Acad Dermatol Venereol, 2015. 29 Suppl 1: p. 3-8., https://www.ncbi.nlm.nih.gov/pubmed/25470718
75. Dirschka, T., Gupta, G., Micali, G., Stockfleth, E., Basset-Seguin, N., Del Marmol, V., et.al. Real-world approach to actinic keratosis management: practical treatment algorithm for office-based dermatology, J Dermatolog Treat, 2017. 28(5): p. 431-442., https://www.ncbi.nlm.nih.gov/pubmed/27796187
76. Einspahr, J., Alberts, D. S., Aickin, M., Welch, K., Bozzo, P., Grogan, T., et.al. Expression of p53 protein in actinic keratosis, adjacent, normal-appearing, and non-sun-exposed human skin, Cancer Epidemiol Biomarkers Prev, 1997. 6(8): p. 583-7., https://www.ncbi.nlm.nih.gov/pubmed/9264270
77. Amirnia, M., Babaie-Ghazani, A., Fakhrjou, A., Khodaeiani, E., Alikhah, H., Naghavi-behzad, M., et.al. Immunohistochemical study of cyclooxygenase-2 in skin tumors, J Dermatolog Treat, 2014. 25(5): p. 380-7., https://www.ncbi.nlm.nih.gov/pubmed/22667343
78. Torres, A., Storey, L., Anders, M., Miller, R. L., Bulbulian, B. J., Jin, J., et.al. Microarray analysis of aberrant gene expression in actinic keratosis: effect of the Toll-like receptor-7 agonist imiquimod, Br J Dermatol, 2007. 157(6): p. 1132-47., https://www.ncbi.nlm.nih.gov/pubmed/17944981
79. Zaravinos, A., Kanellou, P., Baritaki, S., Bonavida, B., Spandidos, D. A., BRAF and RKIP are significantly decreased in cutaneous squamous cell carcinoma, Cell Cycle, 2009. 8(9): p. 1402-8., https://www.ncbi.nlm.nih.gov/pubmed/19342899
80. Roewert-Huber, J., Stockfleth, E., Kerl, H., Pathology and pathobiology of actinic (solar) keratosis - an update, Br J Dermatol, 2007. 157 Suppl 2: p. 18-20., https://www.ncbi.nlm.nih.gov/pubmed/18067626
81. Erlendsson, A. M., Egekvist, H., Lorentzen, H. F., Philipsen, P. A., Stausbol-Gron, B., Stender, I. M., et.al. Actinic keratosis: a cross-sectional study of disease characteristics and treatment patterns in Danish dermatology clinics, Int J Dermatol, 2016. 55(3): p. 309-16., https://www.ncbi.nlm.nih.gov/pubmed/26276415
82. Figueras Nart, I., Cerio, R., Dirschka, T., Dreno, B., Lear, J. T., Pellacani, G., et.al. Defining the actinic keratosis field: a literature review and discussion, J Eur Acad Dermatol Venereol, 2017., https://www.ncbi.nlm.nih.gov/pubmed/29055153
83. Wheller, L., Soyer, H. P., Clinical features of actinic keratoses and early squamous cell carcinoma, Curr Probl Dermatol, 2015. 46: p. 58-63., https://www.ncbi.nlm.nih.gov/pubmed/25561207
84. Huerta-Brogeras, M., Olmos, O., Borbujo, J., Hernandez-Nunez, A., Castano, E., Romero-Mate, A., et.al. Validation of dermoscopy as a real-time noninvasive diagnostic imaging technique for actinic keratosis, Arch Dermatol, 2012. 148(10): p. 1159-64., https://www.ncbi.nlm.nih.gov/pubmed/23069952
85. Akay, B. N., Kocyigit, P., Heper, A. O., Erdem, C., Dermatoscopy of flat pigmented facial lesions: diagnostic challenge between pigmented actinic keratosis and lentigo maligna, Br J Dermatol, 2010. 163(6): p. 1212-7., https://www.ncbi.nlm.nih.gov/pubmed/21083845
86. Lallas, A., Pyne, J., Kyrgidis, A., Andreani, S., Argenziano, G., Cavaller, A., et.al. The clinical and dermoscopic features of invasive cutaneous squamous cell carcinoma depend on the histopathological grade of differentiation, Br J Dermatol, 2015. 172(5): p. 1308-15., https://www.ncbi.nlm.nih.gov/pubmed/25363081
87. Zalaudek, I., Argenziano, G., Dermoscopy of actinic keratosis, intraepidermal carcinoma and squamous cell carcinoma, Curr Probl Dermatol, 2015. 46: p. 70-6., https://www.ncbi.nlm.nih.gov/pubmed/25561209
88. Lallas, A., Tschandl, P., Kyrgidis, A., Stolz, W., Rabinovitz, H., Cameron, A., et.al. Dermoscopic clues to differentiate facial lentigo maligna from pigmented actinic keratosis, Br J Dermatol, 2016. 174(5): p. 1079-85., https://www.ncbi.nlm.nih.gov/pubmed/26784739
89. Welzel, J., Ulrich, M., Lange-Aschenfeldt, S., Stolz, W., Sattler, E., S1-Leitlinie 013-076: Konfokale Lasermikroskopie in der Dermatologie, 2017.
90. Malvehy, J., Alarcon, I., Montoya, J., Rodriguez-Azeredo, R., Puig, S., Treatment monitoring of 0.5% 5-fluorouracil and 10% salicylic acid in clinical and subclinical actinic keratoses with the combination of optical coherence tomography and reflectance confocal microscopy, J Eur Acad Dermatol Venereol, 2016. 30(2): p. 258-65., https://www.ncbi.nlm.nih.gov/pubmed/26538346
91. Malvehy, J., Roldan-Marin, R., Iglesias-Garcia, P., Diaz, A., Puig, S., Monitoring treatment of field cancerisation with 3% diclofenac sodium 2.5% hyaluronic acid by reflectance confocal microscopy: a histologic correlation, Acta Derm Venereol, 2015. 95(1): p. 45-50., https://www.ncbi.nlm.nih.gov/pubmed/24696069
92. Ulrich, M., Alarcon, I., Malvehy, J., Puig, S., In vivo reflectance confocal microscopy characterization of field-directed 5-fluorouracil 0.5%/salicylic acid 10% in actinic keratosis, Dermatology, 2015. 230(3): p. 193-8., https://www.ncbi.nlm.nih.gov/pubmed/25721522
93. Ulrich, M., Krueger-Corcoran, D., Roewert-Huber, J., Sterry, W., Stockfleth, E., Astner, S., Reflectance confocal microscopy for noninvasive monitoring of therapy and detection of subclinical actinic keratoses, Dermatology, 2010. 220(1): p. 15-24., https://www.ncbi.nlm.nih.gov/pubmed/19907131
94. Ulrich, M., Reinhold, U., Skov, T., Elvang Sondergaard, R., Guitera, P., Histological examination confirms clinical clearance of actinic keratoses following treatment with ingenol mebutate 0.05% gel, Br J Dermatol, 2017. 176(1): p. 71-80., https://www.ncbi.nlm.nih.gov/pubmed/27518593
95. Boone, M. A., Marneffe, A., Suppa, M., Miyamoto, M., Alarcon, I., Hofmann-Wellenhof, R., et.al. High-definition optical coherence tomography algorithm for the discrimination of actinic keratosis from normal skin and from squamous cell carcinoma, J Eur Acad Dermatol Venereol, 2015. 29(8): p. 1606-15., https://www.ncbi.nlm.nih.gov/pubmed/25656269
96. Friis, K. B. E., Themstrup, L., Jemec, G. B. E., Optical coherence tomography in the diagnosis of actinic keratosis-A systematic review, Photodiagnosis Photodyn Ther, 2017. 18: p. 98-104., https://www.ncbi.nlm.nih.gov/pubmed/28188920
97. Schuh, S., Kaestle, R., Sattler, E. C., Welzel, J., Optical coherence tomography of actinic keratoses and basal cell carcinomas - differentiation by quantification of signal intensity and layer thickness, J Eur Acad Dermatol Venereol, 2016. 30(8): p. 1321-6., https://www.ncbi.nlm.nih.gov/pubmed/26915996
98. Maier, T., Cekovic, D., Ruzicka, T., Sattler, E. C., Berking, C., Treatment monitoring of topical ingenol mebutate in actinic keratoses with the combination of optical coherence tomography and reflectance confocal microscopy: a case series, Br J Dermatol, 2015. 172(3): p. 816-8., https://www.ncbi.nlm.nih.gov/pubmed/25070046
99. Markowitz, O., Schwartz, M., Feldman, E., Bieber, A., Bienenfeld, A., Nandanan, N., et.al. Defining Field Cancerization of the Skin Using Noninvasive Optical Coherence Tomography Imaging to Detect and Monitor Actinic Keratosis in Ingenol Mebutate 0.015%- Treated Patients, J Clin Aesthet Dermatol, 2016. 9(5): p. 18-25., https://www.ncbi.nlm.nih.gov/pubmed/27386042
100. Themstrup, L., Banzhaf, C. A., Mogensen, M., Jemec, G. B., Optical coherence tomography imaging of non-melanoma skin cancer undergoing photodynamic therapy reveals subclinical residual lesions, Photodiagnosis Photodyn Ther, 2014. 11(1): p. 7-12., https://www.ncbi.nlm.nih.gov/pubmed/24280439
101. Ulrich, M., Lange-Asschenfeldt, S., Skak, K., Skov, T., Osterdal, M. L., Rowert-Huber, H. J., et.al. Biological Effects of Ingenol Mebutate Gel in Moderate to Severe Actinic Fields Assessed by Reflectance Confocal Microscopy: A Phase I Study, J Drugs Dermatol, 2016. 15(10): p. 1181-1189., https://www.ncbi.nlm.nih.gov/pubmed/27741334
102. Nguyen, K. P., Peppelman, M., Hoogedoorn, L., Van Erp, P. E., Gerritsen, M. P., The current role of in vivo reflectance confocal microscopy within the continuum of actinic keratosis and squamous cell carcinoma: a systematic review, Eur J Dermatol, 2016. 26(6): p. 549-565., https://www.ncbi.nlm.nih.gov/pubmed/28007674
103. Ulrich, M., Maltusch, A., Rius-Diaz, F., Rowert-Huber, J., Gonzalez, S., Sterry, W., et.al. Clinical applicability of in vivo reflectance confocal microscopy for the diagnosis of actinic keratoses, Dermatol Surg, 2008. 34(5): p. 610-9., https://www.ncbi.nlm.nih.gov/pubmed/18261097
104. Stratigos, A., Garbe, C., Lebbe, C., Malvehy, J., del Marmol, V., Pehamberger, H., et.al. Diagnosis and treatment of invasive squamous cell carcinoma of the skin: European consensus-based interdisciplinary guideline, Eur J Cancer, 2015. 51(14): p. 1989-2007., https://www.ncbi.nlm.nih.gov/pubmed/26219687
105. Diepgen, T. L., Drexler, H., Elsner, P., Schmitt, J., [UV-irradiation-induced skin cancer as a new occupational disease], Hautarzt, 2015. 66(3): p. 154-9., https://www.ncbi.nlm.nih.gov/pubmed/25737435
106. Bilen, N., Dal, H., Kaur, A. C., Scraping cytology in the diagnosis of malignant squamous neoplasms of the skin, Acta Cytol, 2000. 44(1): p. 101-3., https://www.ncbi.nlm.nih.gov/pubmed/10667170
107. Christensen, E., Bofin, A., Gudmundsdottir, I., Skogvoll, E., Cytological diagnosis of basal cell carcinoma and actinic keratosis, using Papanicolaou and May-Grunwald-Giemsa stained cutaneous tissue smear, Cytopathology, 2008. 19(5): p. 316-22., https://www.ncbi.nlm.nih.gov/pubmed/17916094
108. Vega-Memije, E., De Larios, N. M., Waxtein, L. M., Dominguez-Soto, L., Cytodiagnosis of cutaneous basal and squamous cell carcinoma, Int J Dermatol, 2000. 39(2): p. 116-20., https://www.ncbi.nlm.nih.gov/pubmed/10692060
109. Xing, Y., Cromwell, K. D., Cormier, J. N., Review of diagnostic imaging modalities for the surveillance of melanoma patients, Dermatol Res Pract, 2012. 2012: p. 941921., https://www.ncbi.nlm.nih.gov/pubmed/21876688
110. de Bree, R., Takes, R. P., Castelijns, J. A., Medina, J. E., Stoeckli, S. J., Mancuso, A. A., et.al. Advances in diagnostic modalities to detect occult lymph node metastases in head and neck squamous cell carcinoma, Head Neck, 2015. 37(12): p. 1829-39., https://www.ncbi.nlm.nih.gov/pubmed/24954811
111. Yoon, D. Y., Hwang, H. S., Chang, S. K., Rho, Y. S., Ahn, H. Y., Kim, J. H., et.al. CT, MR, US,18F-FDG PET/CT, and their combined use for the assessment of cervical lymph node metastases in squamous cell carcinoma of the head and neck, Eur Radiol, 2009. 19(3): p. 634-42., https://www.ncbi.nlm.nih.gov/pubmed/18843493
112. Teymoortash, A., Schultz, E.S., Werner , J.A., Klinische Bedeutung parotidealer Metastasen von Plattenepithelkarzinomen der Kopfhaut, Der Hautarzt, 2007. 58(4): p. 323-327., https://doi.org/10.1007/s00105-006-1275-8, https://link.springer.com/content/pdf/10.1007%2Fs00105-006-1275-8.pdf
113. Liao, L. J., Lo, W. C., Hsu, W. L., Wang, C. T., Lai, M. S., Detection of cervical lymph node metastasis in head and neck cancer patients with clinically N0 neck-a meta-analysis comparing different imaging modalities, BMC Cancer, 2012. 12: p. 236., https://www.ncbi.nlm.nih.gov/pubmed/22691269
114. Heusch, P., Sproll, C., Buchbender, C., Rieser, E., Terjung, J., Antke, C., et.al. Diagnostic accuracy of ultrasound, (1)(8)F-FDG-PET/CT, and fused (1)(8)F-FDG-PET-MR images with DWI for the detection of cervical lymph node metastases of HNSCC, Clin Oral Investig, 2014. 18(3): p. 969-78., https://www.ncbi.nlm.nih.gov/pubmed/23892450
115. Diederich, S., [Radiological diagnosis of pulmonary metastases: imaging findings and diagnostic accuracy], Radiologe, 2004. 44(7): p. 663-70., https://www.ncbi.nlm.nih.gov/pubmed/15232688
116. Fischbach, F., Knollmann, F., Griesshaber, V., Freund, T., Akkol, E., Felix, R., Detection of pulmonary nodules by multislice computed tomography: improved detection rate with reduced slice thickness, Eur Radiol, 2003. 13(10): p. 2378-83., https://www.ncbi.nlm.nih.gov/pubmed/12743736
117. Rinne, D., Baum, R. P., Hor, G., Kaufmann, R., Primary staging and follow-up of high risk melanoma patients with whole-body 18F-fluorodeoxyglucose positron emission tomography: results of a prospective study of 100 patients, Cancer, 1998. 82(9): p. 1664-71., https://www.ncbi.nlm.nih.gov/pubmed/9576286
118. Ruiz, E. S., Karia, P. S., Morgan, F. C., Schmults, C. D., The positive impact of radiologic imaging on high-stage cutaneous squamous cell carcinoma management, J Am Acad Dermatol, 2017. 76(2): p. 217-225., https://pubmed.ncbi.nlm.nih.gov/27707594/
119. de Bree, R., Haigentz, M., Jr., Silver, C. E., Paccagnella, D., Hamoir, M., Hartl, D. M., et.al. Distant metastases from head and neck squamous cell carcinoma. Part II. Diagnosis, Oral Oncol, 2012. 48(9): p. 780-6., https://www.ncbi.nlm.nih.gov/pubmed/22520053
120. Rohde, M., Dyrvig, A. K., Johansen, J., Sorensen, J. A., Gerke, O., Nielsen, A. L., et.al. 18F-fluoro-deoxy-glucose-positron emission tomography/computed tomography in diagnosis of head and neck squamous cell carcinoma: a systematic review and meta-analysis, Eur J Cancer, 2014. 50(13): p. 2271-9., https://www.ncbi.nlm.nih.gov/pubmed/25011659
121. Schlittenbauer, T., Zeilinger, M., Nkenke, E., Kreissel, S., Wurm, M. C., Lell, M., et.al. Positron emission tomography-computed tomography versus positron emission tomography-magnetic resonance imaging for diagnosis of oral squamous cell carcinoma: A pilot study, J Craniomaxillofac Surg, 2015. 43(10): p. 2129-35., https://www.ncbi.nlm.nih.gov/pubmed/26498514
122. Senft, A., Hoekstra, O. S., Witte, B. I., Leemans, C. R., de Bree, R., Screening for distant metastases in head and neck cancer patients using FDG-PET and chest CT: validation of an algorithm, Eur Arch Otorhinolaryngol, 2016. 273: p. 2643-50., https://www.ncbi.nlm.nih.gov/pubmed/26350882
123. Lonneux, M., Hamoir, M., Reychler, H., Maingon, P., Duvillard, C., Calais, G., et.al. Positron emission tomography with [18F]fluorodeoxyglucose improves staging and patient management in patients with head and neck squamous cell carcinoma: a multicenter prospective study, J Clin Oncol, 2010. 28(7): p. 1190-5., https://www.ncbi.nlm.nih.gov/pubmed/20124179
124. Fujiwara, Masao, Suzuki, Takahiro, Takiguchi, Tetsuya, Fukamizu, Hidekazu, Tokura, Yoshiki, Evaluation of positron emission tomography imaging to detect lymph node metastases in patients with high-risk cutaneous squamous cell carcinoma, The Journal of Dermatology, 2016. 43(11): p. 1314-1320., http://dx.doi.org/10.1111/1346-8138.13403
125. Mahajan, S, Barker, CA, Singh, B, Pandit-Taskar, N, Clinical value of 18F-FDG-PET/CT in staging cutaneous squamous cell carcinoma., Nucl Med Commun, 2019. 40 (7)(7): p. 744-751., https://pubmed.ncbi.nlm.nih.gov/31095044/
126. Mahajan, S, Barker, CA, Mauguen, A, Singh, B, Pandit-Taskar, N, Restaging [18F] fludeoxyglucose positron emission tomography/computed tomography scan in recurrent cutaneous squamous cell carcinoma: Diagnostic performance and prognostic significance, J Am Acad Dermatol, 2020. 82 (4)(4): p. 878-886., https://pubmed.ncbi.nlm.nih.gov/31562942/
127. Gupta, A. K., Paquet, M., Villanueva, E., Brintnell, W., Interventions for actinic keratoses, Cochrane Database Syst Rev, 2012. 12: p. Cd004415., https://www.ncbi.nlm.nih.gov/pubmed/23235610
128. Werner, R. N., Stockfleth, E., Connolly, S. M., Correia, O., Erdmann, R., Foley, P., et.al. Evidence- and consensus-based (S3) Guidelines for the Treatment of Actinic Keratosis - International League of Dermatological Societies in cooperation with the European Dermatology Forum - Short version, J Eur Acad Dermatol Venereol, 2015. 29(11): p. 2069-79., https://www.ncbi.nlm.nih.gov/pubmed/26370093
129. Marks, R., Rennie, G., Selwood, T. S., Malignant transformation of solar keratoses to squamous cell carcinoma, Lancet, 1988. 1(8589): p. 795-7., https://www.ncbi.nlm.nih.gov/pubmed/2895318
130. Quaedvlieg, P. J., Tirsi, E., Thissen, M. R., Krekels, G. A., Actinic keratosis: how to differentiate the good from the bad ones?, Eur J Dermatol, 2006. 16(4): p. 335-9., https://www.ncbi.nlm.nih.gov/pubmed/16935787
131. Vegter, S., Tolley, K., A network meta-analysis of the relative efficacy of treatments for actinic keratosis of the face or scalp in Europe, PLoS One, 2014. 9(6): p. e96829., https://www.ncbi.nlm.nih.gov/pubmed/24892649
132. Kiefer, C., Sturtz, S., Bender, R., Indirect Comparisons and Network Meta-Analyses, Dtsch Arztebl Int, 2015. 112(47): p. 803-8., https://www.ncbi.nlm.nih.gov/pubmed/26634940
133. Steeb, T, Wessely, A, Schmitz, L, Heppt, F, Kirchberger, MC, Berking, C, et.al. Interventions for Actinic Keratosis in Nonscalp and Nonface Localizations: Results from a Systematic Review with Network Meta-Analysis., J Invest Dermatol, 2021. 141 (2)(2): p. 345-354.e8., https://pubmed.ncbi.nlm.nih.gov/32645365/
134. Ulrich, M., Pellacani, G., Ferrandiz, C., Lear, J. T., Evidence for field cancerisation treatment of actinic keratoses with topical diclofenac in hyaluronic acid, Eur J Dermatol, 2014. 24(2): p. 158-167.
135. Heppt, MV, Steeb, T, Ruzicka, T, Berking, C, Cryosurgery combined with topical interventions for actinic keratosis: a systematic review and meta-analysis., Br J Dermatol, 2019. 180 (4)(4): p. 740-748., https://pubmed.ncbi.nlm.nih.gov/30447074/
136. Heppt, MV, Steeb, T, Leiter, U, Berking, C, Efficacy of photodynamic therapy combined with topical interventions for the treatment of actinic keratosis: a meta-analysis., J Eur Acad Dermatol Venereol, 2019. 33 (5)(5): p. 863-873., https://pubmed.ncbi.nlm.nih.gov/30710390/
137. Steeb, T, Schlager, JG, Kohl, C, Ruzicka, T, Heppt, MV, Berking, C, Laser-assisted photodynamic therapy for actinic keratosis: A systematic review and meta-analysis., J Am Acad Dermatol, 2019. 80 (4)(4): p. 947-956., https://pubmed.ncbi.nlm.nih.gov/30267719/
138. Steeb, T, Koch, EAT, Wessely, A, Wiest, LG, Schmitz, L, Berking, C, et.al. Chemical peelings for the treatment of actinic keratosis: a systematic review and meta-analysis., J Eur Acad Dermatol Venereol, 2021. 35 (3)(3): p. 641-649., https://pubmed.ncbi.nlm.nih.gov/32745330/
139. Foley, P., Merlin, K., Cumming, S., Campbell, J., Crouch, R., Harrison, S., et.al. A comparison of cryotherapy and imiquimod for treatment of actinic keratoses: lesion clearance, safety, and skin quality outcomes, J Drugs Dermatol, 2011. 10(12): p. 1432-8., https://www.ncbi.nlm.nih.gov/pubmed/22134568
140. Krawtchenko, N., Roewert-Huber, J., Ulrich, M., Mann, I., Sterry, W., Stockfleth, E., A randomised study of topical 5% imiquimod vs. topical 5-fluorouracil vs. cryosurgery in immunocompetent patients with actinic keratoses: a comparison of clinical and histological outcomes including 1-year follow-up, Br J Dermatol, 2007. 157 Suppl 2: p. 34-40., https://www.ncbi.nlm.nih.gov/pubmed/18067630
141. Morton, C., Campbell, S., Gupta, G., Keohane, S., Lear, J., Zaki, I., et.al. Intraindividual, right-left comparison of topical methyl aminolaevulinate-photodynamic therapy and cryotherapy in subjects with actinic keratoses: a multicentre, randomized controlled study, Br J Dermatol, 2006. 155(5): p. 1029-36., https://www.ncbi.nlm.nih.gov/pubmed/17034536
142. Simon, J. C., Dominicus, R., Karl, L., Rodriguez, R., Willers, C., Dirschka, T., A prospective randomized exploratory study comparing the efficacy of once-daily topical 0.5% 5-fluorouracil in combination with 10.0% salicylic acid (5-FU/SA) vs. cryosurgery for the treatment of hyperkeratotic actinic keratosis, J Eur Acad Dermatol Venereol, 2015. 29(5): p. 881-9., https://www.ncbi.nlm.nih.gov/pubmed/25257941
143. Zane, C., Facchinetti, E., Rossi, M. T., Specchia, C., Ortel, B., Calzavara-Pinton, P., Cryotherapy is preferable to ablative CO2 laser for the treatment of isolated actinic keratoses of the face and scalp: a randomized clinical trial, Br J Dermatol, 2014. 170(5): p. 1114-21., https://www.ncbi.nlm.nih.gov/pubmed/24472087
144. Kaufmann, R., Spelman, L., Weightman, W., Reifenberger, J., Szeimies, R. M., Verhaeghe, E., et.al. Multicentre intraindividual randomized trial of topical methyl aminolaevulinate-photodynamic therapy vs. cryotherapy for multiple actinic keratoses on the extremities, Br J Dermatol, 2008. 158(5): p. 994-9., https://www.ncbi.nlm.nih.gov/pubmed/18341663
145. Askew, D. A., Mickan, S. M., Soyer, H. P., Wilkinson, D., Effectiveness of 5-fluorouracil treatment for actinic keratosis--a systematic review of randomized controlled trials, Int J Dermatol, 2009. 48(5): p. 453-63., https://www.ncbi.nlm.nih.gov/pubmed/19416373
146. Freeman, M., Vinciullo, C., Francis, D., Spelman, L., Nguyen, R., Fergin, P., et.al. A comparison of photodynamic therapy using topical methyl aminolevulinate (Metvix) with single cycle cryotherapy in patients with actinic keratosis: a prospective, randomized study, J Dermatolog Treat, 2003. 14(2): p. 99-106., https://www.ncbi.nlm.nih.gov/pubmed/12775317
147. Szeimies, R. M., Karrer, S., Radakovic-Fijan, S., Tanew, A., Calzavara-Pinton, P. G., Zane, C., et.al. Photodynamic therapy using topical methyl 5-aminolevulinate compared with cryotherapy for actinic keratosis: A prospective, randomized study, J Am Acad Dermatol, 2002. 47(2): p. 258-62., https://www.ncbi.nlm.nih.gov/pubmed/12140473
148. Holzer, G., Pinkowicz, A., Radakovic, S., Schmidt, J. B., Tanew, A., Randomized controlled trial comparing 35% trichloroacetic acid peel and 5-aminolaevulinic acid photodynamic therapy for treating multiple actinic keratosis, Br J Dermatol, 2017. 176(5): p. 1155-1161., https://www.ncbi.nlm.nih.gov/pubmed/28012181
149. Lawrence, N, Cox, SE, Cockerell, CJ, Freeman, RG, Cruz, PD, A comparison of the efficacy and safety of Jessner's solution and 35% trichloroacetic acid vs 5% fluorouracil in the treatment of widespread facial actinic keratoses., Arch Dermatol, 1995. 131 (2)(2): p. 176-81., https://pubmed.ncbi.nlm.nih.gov/7857114/
150. Di Nuzzo, S, Cortelazzi, C, Boccaletti, V, Zucchi, A, Conti, ML, Montanari, P, et.al. Comparative study of trichloroacetic acid vs. photodynamic therapy with topical 5-aminolevulinic acid for actinic keratosis of the scalp., Photodermatol Photoimmunol Photomed, 2015. 31 (5)(5): p. 233-8., https://pubmed.ncbi.nlm.nih.gov/25660106/
151. Coleman, W. P., 3rd, Yarborough, J. M., Mandy, S. H., Dermabrasion for prophylaxis and treatment of actinic keratoses, Dermatol Surg, 1996. 22(1): p. 17-21., https://www.ncbi.nlm.nih.gov/pubmed/8556252
152. Salehi Farid, A, Niknam, S, Gholami, K, Tavakolpour, S, Teimourpour, A, Daneshpazhooh, M, et.al. Comparing efficacy and safety of potassium hydroxide 5% solution with 5-fluorouracil cream in patients with actinic keratoses: a randomized controlled trial., J Dermatolog Treat, 2020. (): p. 1-7., https://pubmed.ncbi.nlm.nih.gov/32875946/
153. Reinhold, U, Bai-Habelski, J, Abeck, D, Denfeld, R, Dominicus, R, Fischer, T, et.al. [Potassium hydroxide 5 % solution in actinic keratosis : A novel therapeutic approach in the lesion-directed treatment]., Hautarzt, 2021. ():, https://pubmed.ncbi.nlm.nih.gov/34387709/
154. Ostertag, J. U., Quaedvlieg, P. J., van der Geer, S., Nelemans, P., Christianen, M. E., Neumann, M. H., et.al. A clinical comparison and long-term follow-up of topical 5-fluorouracil versus laser resurfacing in the treatment of widespread actinic keratoses, Lasers Surg Med, 2006. 38(8): p. 731-9., https://www.ncbi.nlm.nih.gov/pubmed/16912977
155. Sierra, H., Yelamos, O., Cordova, M., Chen, C. J., Rajadhyaksha, M., Reflectance confocal microscopy-guided laser ablation of basal cell carcinomas: initial clinical experience, J Biomed Opt, 2017. 22(8): p. 1-13., https://www.ncbi.nlm.nih.gov/pubmed/28831793
156. Sierra, H., Damanpour, S., Hibler, B., Nehal, K., Rossi, A., Rajadhyaksha, M., Confocal imaging of carbon dioxide laser-ablated basal cell carcinomas: An ex-vivo study on the uptake of contrast agent and ablation parameters, Lasers Surg Med, 2016. 48(2): p. 133-9., https://www.ncbi.nlm.nih.gov/pubmed/26392001
157. Hantash, B. M., Stewart, D. B., Cooper, Z. A., Rehmus, W. E., Koch, R. J., Swetter, S. M., Facial resurfacing for nonmelanoma skin cancer prophylaxis, Arch Dermatol, 2006. 142(8): p. 976-82., https://www.ncbi.nlm.nih.gov/pubmed/16924046
158. Nguyen, B. T., Gan, S. D., Konnikov, N., Liang, C. A., Treatment of superficial basal cell carcinoma and squamous cell carcinoma in situ on the trunk and extremities with ablative fractional laser-assisted delivery of topical fluorouracil, J Am Acad Dermatol, 2015. 72(3): p. 558-60., https://www.ncbi.nlm.nih.gov/pubmed/25687314
159. Karmisholt, K. E., Haedersdal, M., Ablative fractional laser intensifies treatment outcome of scalp actinic keratoses with ingenol mebutate: a case report, J Eur Acad Dermatol Venereol, 2016. 30(5): p. 854-5., https://www.ncbi.nlm.nih.gov/pubmed/25732962
160. Ko, D. Y., Jeon, S. Y., Kim, K. H., Song, K. H., Fractional erbium: YAG laser-assisted photodynamic therapy for facial actinic keratoses: a randomized, comparative, prospective study, J Eur Acad Dermatol Venereol, 2014. 28(11): p. 1529-39., https://www.ncbi.nlm.nih.gov/pubmed/24341367
161. Togsverd-Bo, K., Haak, C. S., Thaysen-Petersen, D., Wulf, H. C., Anderson, R. R., Haedersdal, M., Intensified photodynamic therapy of actinic keratoses with fractional CO2 laser: a randomized clinical trial, Br J Dermatol, 2012. 166(6): p. 1262-9., https://www.ncbi.nlm.nih.gov/pubmed/22348388
162. Helsing, P., Togsverd-Bo, K., Veierod, M. B., Mork, G., Haedersdal, M., Intensified fractional CO2 laser-assisted photodynamic therapy vs. laser alone for organ transplant recipients with multiple actinic keratoses and wart-like lesions: a randomized half-side comparative trial on dorsal hands, Br J Dermatol, 2013. 169(5): p. 1087-92., https://pubmed.ncbi.nlm.nih.gov/23855503/
163. Lapidoth, M., Adatto, M., Halachmi, S., Treatment of actinic keratoses and photodamage with non-contact fractional 1540-nm laser quasi-ablation: an ex vivo and clinical evaluation, Lasers Med Sci, 2013. 28(2): p. 537-42., https://www.ncbi.nlm.nih.gov/pubmed/22538843
164. Alexiades-Armenakas, M. R., Geronemus, R. G., Laser-mediated photodynamic therapy of actinic keratoses, Arch Dermatol, 2003. 139(10): p. 1313-20., https://www.ncbi.nlm.nih.gov/pubmed/14568836
165. Moskalik, K., Kozlow, A., Demin, E., Boiko, E., Powerful neodymium laser radiation for the treatment of facial carcinoma: 5 year follow-up data, Eur J Dermatol, 2010. 20(6): p. 738-42., https://www.ncbi.nlm.nih.gov/pubmed/21056940
166. Akarsu, S., Aktan, S., Atahan, A., Koc, P., Ozkan, S., Comparison of topical 3% diclofenac sodium gel and 5% imiquimod cream for the treatment of actinic keratoses, Clin Exp Dermatol, 2011. 36(5): p. 479-84., https://www.ncbi.nlm.nih.gov/pubmed/21418281
167. Gebauer, K., Brown, P., Varigos, G., Topical diclofenac in hyaluronan gel for the treatment of solar keratoses, Australas J Dermatol, 2003. 44(1): p. 40-3., https://www.ncbi.nlm.nih.gov/pubmed/12581080
168. Kose, O., Koc, E., Erbil, A. H., Caliskan, E., Kurumlu, Z., Comparison of the efficacy and tolerability of 3% diclofenac sodium gel and 5% imiquimod cream in the treatment of actinic keratosis, J Dermatolog Treat, 2008. 19(3): p. 159-63., https://www.ncbi.nlm.nih.gov/pubmed/18569272
169. McEwan, L. E., Smith, J. G., Topical diclofenac/hyaluronic acid gel in the treatment of solar keratoses, Australas J Dermatol, 1997. 38(4): p. 187-9., https://www.ncbi.nlm.nih.gov/pubmed/9431711
170. Rivers, J. K., Arlette, J., Shear, N., Guenther, L., Carey, W., Poulin, Y., Topical treatment of actinic keratoses with 3.0% diclofenac in 2.5% hyaluronan gel, Br J Dermatol, 2002. 146(1): p. 94-100., https://www.ncbi.nlm.nih.gov/pubmed/11841372
171. Segatto, M. M., Dornelles, S. I., Silveira, V. B., Frantz Gde, O., Comparative study of actinic keratosis treatment with 3% diclofenac sodium and 5% 5-fluorouracil, An Bras Dermatol, 2013. 88(5): p. 732-8., https://www.ncbi.nlm.nih.gov/pubmed/24173178
172. Ulrich, C., Johannsen, A., Rowert-Huber, J., Ulrich, M., Sterry, W., Stockfleth, E., Results of a randomized, placebo-controlled safety and efficacy study of topical diclofenac 3% gel in organ transplant patients with multiple actinic keratoses, Eur J Dermatol, 2010. 20(4): p. 482-8., https://www.ncbi.nlm.nih.gov/pubmed/20507841
173. Wolf, J. E., Jr., Taylor, J. R., Tschen, E., Kang, S., Topical 3.0% diclofenac in 2.5% hyaluronan gel in the treatment of actinic keratoses, Int J Dermatol, 2001. 40(11): p. 709-13., https://www.ncbi.nlm.nih.gov/pubmed/11737438
174. Zane, C., Facchinetti, E., Rossi, M. T., Specchia, C., Calzavara-Pinton, P. G., A randomized clinical trial of photodynamic therapy with methyl aminolaevulinate vs. diclofenac 3% plus hyaluronic acid gel for the treatment of multiple actinic keratoses of the face and scalp, Br J Dermatol, 2014. 170(5): p. 1143-50., https://www.ncbi.nlm.nih.gov/pubmed/24506666
175. Stockfleth, E., Kerl, H., Zwingers, T., Willers, C., Low-dose 5-fluorouracil in combination with salicylic acid as a new lesion-directed option to treat topically actinic keratoses: histological and clinical study results, Br J Dermatol, 2011. 165(5): p. 1101-8., https://www.ncbi.nlm.nih.gov/pubmed/21517801
176. Pflugfelder, A., Welter, A. K., Leiter, U., Weide, B., Held, L., Eigentler, T. K., et.al. Open label randomized study comparing 3 months vs. 6 months treatment of actinic keratoses with 3% diclofenac in 2.5% hyaluronic acid gel: a trial of the German Dermatologic Cooperative Oncology Group, J Eur Acad Dermatol Venereol, 2012. 26(1): p. 48-53., https://www.ncbi.nlm.nih.gov/pubmed/21414035
177. Gollnick, H, Dirschka, T, Ostendorf, R, Kerl, H, Kunstfeld, R, Long-term clinical outcomes of imiquimod 5% cream vs. diclofenac 3% gel for actinic keratosis on the face or scalp: a pooled analysis of two randomized controlled trials., J Eur Acad Dermatol Venereol, 2020. 34 (1)(1): p. 82-89., https://pubmed.ncbi.nlm.nih.gov/31407414/
178. Stockfleth, E, Harwood, CA, Serra-Guillén, C, Larsson, T, Østerdal, ML, Skov, T, Phase IV head-to-head randomized controlled trial comparing ingenol mebutate 0·015% gel with diclofenac sodium 3% gel for the treatment of actinic keratosis on the face or scalp., Br J Dermatol, 2018. 178 (2)(2): p. 433-442., https://pubmed.ncbi.nlm.nih.gov/29030864/
179. Ezzedine, K, Painchault, C, Brignone, M, Systematic Literature Review and Network Meta-analysis of the Efficacy and Acceptability of Interventions in Actinic Keratoses., Acta Derm Venereol, 2021. 101 (1)(1): p. adv00358., https://pubmed.ncbi.nlm.nih.gov/33170301/
180. Stockfleth, E., Zwingers, T., Willers, C., Recurrence rates and patient assessed outcomes of 0.5% 5-fluorouracil in combination with salicylic acid treating actinic keratoses, Eur J Dermatol, 2012. 22(3): p. 370-4., https://www.ncbi.nlm.nih.gov/pubmed/22494856
181. Loven, K., Stein, L., Furst, K., Levy, S., Evaluation of the efficacy and tolerability of 0.5% fluorouracil cream and 5% fluorouracil cream applied to each side of the face in patients with actinic keratosis, Clin Ther, 2002. 24(6): p. 990-1000., https://www.ncbi.nlm.nih.gov/pubmed/12117087
182. Pomerantz, H., Hogan, D., Eilers, D., Swetter, S. M., Chen, S. C., Jacob, S. E., et.al. Long-term Efficacy of Topical Fluorouracil Cream, 5%, for Treating Actinic Keratosis: A Randomized Clinical Trial, JAMA Dermatol, 2015. 151(9): p. 952-60., https://www.ncbi.nlm.nih.gov/pubmed/25950503
183. Tanghetti, E., Werschler, P., Comparison of 5% 5-fluorouracil cream and 5% imiquimod cream in the management of actinic keratoses on the face and scalp, J Drugs Dermatol, 2007. 6(2): p. 144-7., https://www.ncbi.nlm.nih.gov/pubmed/17373172
184. Jansen, MHE, Kessels, JPHM, Nelemans, PJ, Kouloubis, N, Arits, AHMM, van Pelt, HPA, et.al. Randomized Trial of Four Treatment Approaches for Actinic Keratosis., N Engl J Med, 2019. 380 (10)(10): p. 935-946., https://pubmed.ncbi.nlm.nih.gov/30855743/
185. Wu, Y, Tang, N, Cai, L, Li, Q, Relative efficacy of 5-fluorouracil compared with other treatments among patients with actinic keratosis: A network meta-analysis., Dermatol Ther, 2019. 32 (3)(3): p. e12822., https://pubmed.ncbi.nlm.nih.gov/30638294/
186. Smith, S., Piacquadio, D., Morhenn, V., Atkin, D., Fitzpatrick, R., Short incubation PDT versus 5-FU in treating actinic keratoses, J Drugs Dermatol, 2003. 2(6): p. 629-35., https://www.ncbi.nlm.nih.gov/pubmed/14711141
187. Jansen, MHE, Kessels, JPHM, Merks, I, Nelemans, PJ, Kelleners-Smeets, NWJ, Mosterd, K, et.al. A trial-based cost-effectiveness analysis of topical 5-fluorouracil vs. imiquimod vs. ingenol mebutate vs. methyl aminolaevulinate conventional photodynamic therapy for the treatment of actinic keratosis in the head and neck area performed in the Netherlands., Br J Dermatol, 2020. 183 (4)(4): p. 738-744., https://pubmed.ncbi.nlm.nih.gov/31961446/
188. Dohil, MA, Efficacy, Safety, and Tolerability of 4% 5-Fluorouracil Cream in a Novel Patented Aqueous Cream Containing Peanut Oil Once Daily Compared With 5% 5-Fluorouracil Cream Twice Daily: Meeting the Challenge in the Treatment of Actinic Keratosis., J Drugs Dermatol, 2016. 15 (10)(10): p. 1218-1224., https://pubmed.ncbi.nlm.nih.gov/27741339/
189. Jorizzo, J., Stewart, D., Bucko, A., Davis, S. A., Espy, P., Hino, P., et.al. Randomized trial evaluating a new 0.5% fluorouracil formulation demonstrates efficacy after 1-, 2-, or 4-week treatment in patients with actinic keratosis, Cutis, 2002. 70(6): p. 335-9., https://www.ncbi.nlm.nih.gov/pubmed/12502122
190. Weiss, J., Menter, A., Hevia, O., Jones, T., Ling, M., Rist, T., et.al. Effective treatment of actinic keratosis with 0.5% fluorouracil cream for 1, 2, or 4 weeks, Cutis, 2002. 70(2 Suppl): p. 22-9., https://www.ncbi.nlm.nih.gov/pubmed/12353677
191. Rahvar, M., Lamel, S. A., Maibach, H. I., Randomized, vehicle-controlled trials of topical 5-fluorouracil therapy for actinic keratosis treatment: an overview, Immunotherapy, 2012. 4(9): p. 939-45., https://www.ncbi.nlm.nih.gov/pubmed/23046237
192. Jorizzo, J., Weiss, J., Furst, K., VandePol, C., Levy, S. F., Effect of a 1-week treatment with 0.5% topical fluorouracil on occurrence of actinic keratosis after cryosurgery: a randomized, vehicle-controlled clinical trial, Arch Dermatol, 2004. 140(7): p. 813-6., https://www.ncbi.nlm.nih.gov/pubmed/15262691
193. Jorizzo, J., Weiss, J., Vamvakias, G., One-week treatment with 0.5% fluorouracil cream prior to cryosurgery in patients with actinic keratoses: a double-blind, vehicle-controlled, long-term study, J Drugs Dermatol, 2006. 5(2): p. 133-9., https://www.ncbi.nlm.nih.gov/pubmed/16485881
194. Levy, S., Furst, K., Chern, W., A pharmacokinetic evaluation of 0.5% and 5% fluorouracil topical cream in patients with actinic keratosis, Clin Ther, 2001. 23(6): p. 908-20., https://www.ncbi.nlm.nih.gov/pubmed/11440290
195. Samorano, L. P., Torezan, L. A., Sanches, J. A., Evaluation of the tolerability and safety of a 0.015% ingenol mebutate gel compared to 5% 5-fluorouracil cream for the treatment of facial actinic keratosis: a prospective randomized trial, J Eur Acad Dermatol Venereol, 2015. 29(9): p. 1822-7., https://www.ncbi.nlm.nih.gov/pubmed/25727104
196. Stockfleth, E., von Kiedrowski, R., Dominicus, R., Ryan, J., Ellery, A., Falques, M., et.al. Efficacy and Safety of 5-Fluorouracil 0.5%/Salicylic Acid 10% in the Field-Directed Treatment of Actinic Keratosis: A Phase III, Randomized, Double-Blind, Vehicle-Controlled Trial, Dermatol Ther (Heidelb), 2017. 7(1): p. 81-96., https://www.ncbi.nlm.nih.gov/pubmed/27995485
197. Stockfleth, E., Sibbring, G. C., Alarcon, I., New Topical Treatment Options for Actinic Keratosis: A Systematic Review, Acta Derm Venereol, 2016. 96(1): p. 17-22., https://www.ncbi.nlm.nih.gov/pubmed/26068001
198. Lebwohl, M., Swanson, N., Anderson, L. L., Melgaard, A., Xu, Z., Berman, B., Ingenol mebutate gel for actinic keratosis, N Engl J Med, 2012. 366(11): p. 1010-9., https://www.ncbi.nlm.nih.gov/pubmed/22417254
199. Garbe, C., Basset-Seguin, N., Poulin, Y., Larsson, T., Osterdal, M. L., Venkata, R., et.al. Efficacy and safety of follow-up field treatment of actinic keratosis with ingenol mebutate 0.015% gel: a randomized, controlled 12-month study, Br J Dermatol, 2016. 174(3): p. 505-13., https://www.ncbi.nlm.nih.gov/pubmed/26471889
200. Lebwohl, M., Shumack, S., Stein Gold, L., Melgaard, A., Larsson, T., Tyring, S. K., Long-term follow-up study of ingenol mebutate gel for the treatment of actinic keratoses, JAMA Dermatol, 2013. 149(6): p. 666-70., https://www.ncbi.nlm.nih.gov/pubmed/23553119
201. Anderson, L., Schmieder, G. J., Werschler, W. P., Tschen, E. H., Ling, M. R., Stough, D. B., et.al. Randomized, double-blind, double-dummy, vehicle-controlled study of ingenol mebutate gel 0.025% and 0.05% for actinic keratosis, J Am Acad Dermatol, 2009. 60(6): p. 934-43., https://www.ncbi.nlm.nih.gov/pubmed/19467365
202. Pellacani, G., Peris, K., Guillen, C., Clonier, F., Larsson, T., Venkata, R., et.al. A randomized trial comparing simultaneous vs. sequential field treatment of actinic keratosis with ingenol mebutate on two separate areas of the head and body, J Eur Acad Dermatol Venereol, 2015. 29(11): p. 2192-8., https://www.ncbi.nlm.nih.gov/pubmed/26300464
203. Zane, C., Fabiano, A., Arisi, M., Calzavara-Pinton, P., A Randomized Split-Face Clinical Trial of Photodynamic Therapy with Methyl Aminolevulinate versus Ingenol Mebutate Gel for the Treatment of Multiple Actinic Keratoses of the Face and Scalp, Dermatology, 2016. 232(4): p. 472-7., https://www.ncbi.nlm.nih.gov/pubmed/27578305
204. Moggio, E., Arisi, M., Zane, C., Calzavara-Pinton, I., Calzavara-Pinton, P., A randomized split-face clinical trial analyzing daylight photodynamic therapy with methyl aminolaevulinate vs ingenol mebutate gel for the treatment of multiple actinic keratoses of the face and the scalp, Photodiagnosis Photodyn Ther, 2016. 16: p. 161-165., https://www.ncbi.nlm.nih.gov/pubmed/27530375
205. Sinnya, S., Tan, J. M., Prow, T. W., Primiero, C., McEniery, E., Selmer, J., et.al. A randomized, phase IIa exploratory trial to assess the safety and preliminary efficacy of LEO 43204 in patients with actinic keratosis, Br J Dermatol, 2016. 174(2): p. 305-11., https://www.ncbi.nlm.nih.gov/pubmed/26499175
206. Alomar, A., Bichel, J., McRae, S., Vehicle-controlled, randomized, double-blind study to assess safety and efficacy of imiquimod 5% cream applied once daily 3 days per week in one or two courses of treatment of actinic keratoses on the head, Br J Dermatol, 2007. 157(1): p. 133-41., https://www.ncbi.nlm.nih.gov/pubmed/17501955
207. Gebauer, K., Shumack, S., Cowen, P. S., Effect of dosing frequency on the safety and efficacy of imiquimod 5% cream for treatment of actinic keratosis on the forearms and hands: a phase II, randomized placebo-controlled trial, Br J Dermatol, 2009. 161(4): p. 897-903., https://www.ncbi.nlm.nih.gov/pubmed/19545297
208. Jorizzo, J., Dinehart, S., Matheson, R., Moore, J. K., Ling, M., Fox, T. L., et.al. Vehicle-controlled, double-blind, randomized study of imiquimod 5% cream applied 3 days per week in one or two courses of treatment for actinic keratoses on the head, J Am Acad Dermatol, 2007. 57(2): p. 265-8., https://www.ncbi.nlm.nih.gov/pubmed/17512087
209. Korman, N., Moy, R., Ling, M., Matheson, R., Smith, S., McKane, S., et.al. Dosing with 5% imiquimod cream 3 times per week for the treatment of actinic keratosis: results of two phase 3, randomized, double-blind, parallel-group, vehicle-controlled trials, Arch Dermatol, 2005. 141(4): p. 467-73., https://www.ncbi.nlm.nih.gov/pubmed/15837864
210. Lebwohl, M., Dinehart, S., Whiting, D., Lee, P. K., Tawfik, N., Jorizzo, J., et.al. Imiquimod 5% cream for the treatment of actinic keratosis: results from two phase III, randomized, double-blind, parallel group, vehicle-controlled trials, J Am Acad Dermatol, 2004. 50(5): p. 714-21., https://www.ncbi.nlm.nih.gov/pubmed/15097955
211. Stockfleth, E., Meyer, T., Benninghoff, B., Salasche, S., Papadopoulos, L., Ulrich, C., et.al. A randomized, double-blind, vehicle-controlled study to assess 5% imiquimod cream for the treatment of multiple actinic keratoses, Arch Dermatol, 2002. 138(11): p. 1498-502., https://www.ncbi.nlm.nih.gov/pubmed/12437457
212. Szeimies, R. M., Gerritsen, M. J., Gupta, G., Ortonne, J. P., Serresi, S., Bichel, J., et.al. Imiquimod 5% cream for the treatment of actinic keratosis: results from a phase III, randomized, double-blind, vehicle-controlled, clinical trial with histology, J Am Acad Dermatol, 2004. 51(4): p. 547-55., https://www.ncbi.nlm.nih.gov/pubmed/15389189
213. Hadley, G., Derry, S., Moore, R. A., Imiquimod for actinic keratosis: systematic review and meta-analysis, J Invest Dermatol, 2006. 126(6): p. 1251-5., https://www.ncbi.nlm.nih.gov/pubmed/16557235
214. Chen, K., Yap, L. M., Marks, R., Shumack, S., Short-course therapy with imiquimod 5% cream for solar keratoses: a randomized controlled trial, Australas J Dermatol, 2003. 44(4): p. 250-5., https://www.ncbi.nlm.nih.gov/pubmed/14616490
215. Ooi, T., Barnetson, R. S., Zhuang, L., McKane, S., Lee, J. H., Slade, H. B., et.al. Imiquimod-induced regression of actinic keratosis is associated with infiltration by T lymphocytes and dendritic cells: a randomized controlled trial, Br J Dermatol, 2006. 154(1): p. 72-8., https://www.ncbi.nlm.nih.gov/pubmed/16403097
216. Ortonne, J. P., Gupta, G., Ortonne, N., Duteil, L., Queille, C., Mallefet, P., Effectiveness of cross polarized light and fluorescence diagnosis for detection of sub-clinical and clinical actinic keratosis during imiquimod treatment, Exp Dermatol, 2010. 19(7): p. 641-7., https://www.ncbi.nlm.nih.gov/pubmed/20201959
217. Ulrich, C., Bichel, J., Euvrard, S., Guidi, B., Proby, C. M., van de Kerkhof, P. C., et.al. Topical immunomodulation under systemic immunosuppression: results of a multicentre, randomized, placebo-controlled safety and efficacy study of imiquimod 5% cream for the treatment of actinic keratoses in kidney, heart, and liver transplant patients, Br J Dermatol, 2007. 157 Suppl 2: p. 25-31., https://www.ncbi.nlm.nih.gov/pubmed/18067628
218. Swanson, N., Abramovits, W., Berman, B., Kulp, J., Rigel, D. S., Levy, S., Imiquimod 2.5% and 3.75% for the treatment of actinic keratoses: results of two placebo-controlled studies of daily application to the face and balding scalp for two 2-week cycles, J Am Acad Dermatol, 2010. 62(4): p. 582-90., https://www.ncbi.nlm.nih.gov/pubmed/20133013
219. Hanke, C. W., Beer, K. R., Stockfleth, E., Wu, J., Rosen, T., Levy, S., Imiquimod 2.5% and 3.75% for the treatment of actinic keratoses: results of two placebo-controlled studies of daily application to the face and balding scalp for two 3-week cycles, J Am Acad Dermatol, 2010. 62(4): p. 573-81., https://www.ncbi.nlm.nih.gov/pubmed/20133012
220. Peris, K., Stockfleth, E., Gupta, G., Aractingi, S., Dakovic, R., Dirschka, T., et.al. Efficacy of imiquimod 3.75% from Lmax according to the number of actinic keratosis lesions, J Eur Acad Dermatol Venereol, 2015. 29(12): p. 2470-3., https://www.ncbi.nlm.nih.gov/pubmed/26954313
221. Blauvelt, A, Kempers, S, Lain, E, Schlesinger, T, Tyring, S, Forman, S, et.al. Phase 3 Trials of Tirbanibulin Ointment for Actinic Keratosis., N Engl J Med, 2021. 384 (6)(6): p. 512-520., https://pubmed.ncbi.nlm.nih.gov/33567191/
222. Smolinski, MP, Bu, Y, Clements, J, Gelman, IH, Hegab, T, Cutler, DL, et.al. Discovery of Novel Dual Mechanism of Action Src Signaling and Tubulin Polymerization Inhibitors (KX2-391 and KX2-361)., J Med Chem, 2018. 61 (11)(11): p. 4704-4719., https://pubmed.ncbi.nlm.nih.gov/29617135/
223. Apalla, Z., Sotiriou, E., Panagiotidou, D., Lefaki, I., Goussi, C., Ioannides, D., The impact of different fluence rates on pain and clinical outcome in patients with actinic keratoses treated with photodynamic therapy, Photodermatol Photoimmunol Photomed, 2011. 27(4): p. 181-5., https://www.ncbi.nlm.nih.gov/pubmed/21729165
224. Giehl, K. A., Kriz, M., Grahovac, M., Ruzicka, T., Berking, C., A controlled trial of photodynamic therapy of actinic keratosis comparing different red light sources, Eur J Dermatol, 2014. 24(3): p. 335-41., https://www.ncbi.nlm.nih.gov/pubmed/24876164
225. Jeffes, E. W., McCullough, J. L., Weinstein, G. D., Kaplan, R., Glazer, S. D., Taylor, J. R., Photodynamic therapy of actinic keratoses with topical aminolevulinic acid hydrochloride and fluorescent blue light, J Am Acad Dermatol, 2001. 45(1): p. 96-104., https://www.ncbi.nlm.nih.gov/pubmed/11423841
226. Pariser, D. M., Houlihan, A., Ferdon, M. B., Berg, J. E., Randomized Vehicle-Controlled Study of Short Drug Incubation Aminolevulinic Acid Photodynamic Therapy for Actinic Keratoses of the Face or Scalp, Dermatol Surg, 2016. 42(3): p. 296-304., https://www.ncbi.nlm.nih.gov/pubmed/26863596
227. Piacquadio, D. J., Chen, D. M., Farber, H. F., Fowler, J. F., Jr., Glazer, S. D., Goodman, J. J., et.al. Photodynamic therapy with aminolevulinic acid topical solution and visible blue light in the treatment of multiple actinic keratoses of the face and scalp: investigator-blinded, phase 3, multicenter trials, Arch Dermatol, 2004. 140(1): p. 41-6., https://www.ncbi.nlm.nih.gov/pubmed/14732659
228. Schmieder, G. J., Huang, E. Y., Jarratt, M., A multicenter, randomized, vehicle-controlled phase 2 study of blue light photodynamic therapy with aminolevulinic acid HCl 20% topical solution for the treatment of actinic keratoses on the upper extremities: the effect of occlusion during the drug incubation period, J Drugs Dermatol, 2012. 11(12): p. 1483-9., https://www.ncbi.nlm.nih.gov/pubmed/23377520
229. Taub, A. F., Garretson, C. B., A randomized, blinded, bilateral intraindividual, vehicle-controlled trial of the use of photodynamic therapy with 5-aminolevulinic acid and blue light for the treatment of actinic keratoses of the upper extremities, J Drugs Dermatol, 2011. 10(9): p. 1049-56., https://www.ncbi.nlm.nih.gov/pubmed/22052276
230. Moloney, F. J., Collins, P., Randomized, double-blind, prospective study to compare topical 5-aminolaevulinic acid methylester with topical 5-aminolaevulinic acid photodynamic therapy for extensive scalp actinic keratosis, Br J Dermatol, 2007. 157(1): p. 87-91., https://www.ncbi.nlm.nih.gov/pubmed/17501954
231. Szeimies, R. M., Radny, P., Sebastian, M., Borrosch, F., Dirschka, T., Krahn-Senftleben, G., et.al. Photodynamic therapy with BF-200 ALA for the treatment of actinic keratosis: results of a prospective, randomized, double-blind, placebo-controlled phase III study, Br J Dermatol, 2010. 163(2): p. 386-94., https://www.ncbi.nlm.nih.gov/pubmed/20518784
232. Dirschka, T., Radny, P., Dominicus, R., Mensing, H., Bruning, H., Jenne, L., et.al. Long-term (6 and 12 months) follow-up of two prospective, randomized, controlled phase III trials of photodynamic therapy with BF-200 ALA and methyl aminolaevulinate for the treatment of actinic keratosis, Br J Dermatol, 2013. 168(4): p. 825-36., https://www.ncbi.nlm.nih.gov/pubmed/23252768
233. Dirschka, T., Radny, P., Dominicus, R., Mensing, H., Bruning, H., Jenne, L., et.al. Photodynamic therapy with BF-200 ALA for the treatment of actinic keratosis: results of a multicentre, randomized, observer-blind phase III study in comparison with a registered methyl-5-aminolaevulinate cream and placebo, Br J Dermatol, 2012. 166(1): p. 137-46., https://www.ncbi.nlm.nih.gov/pubmed/21910711
234. Reinhold, U., Dirschka, T., Ostendorf, R., Aschoff, R., Berking, C., Philipp-Dormston, W. G., et.al. A randomized, double-blind, phase III, multicentre study to evaluate the safety and efficacy of BF-200 ALA (Ameluz((R)) ) vs. placebo in the field-directed treatment of mild-to-moderate actinic keratosis with photodynamic therapy (PDT) when using the BF-RhodoLED((R)) lamp, Br J Dermatol, 2016. 175(4): p. 696-705., https://pubmed.ncbi.nlm.nih.gov/26921093/
235. Szeimies, R. M., Matheson, R. T., Davis, S. A., Bhatia, A. C., Frambach, Y., Klovekorn, W., et.al. Topical methyl aminolevulinate photodynamic therapy using red light-emitting diode light for multiple actinic keratoses: a randomized study, Dermatol Surg, 2009. 35(4): p. 586-92., https://www.ncbi.nlm.nih.gov/pubmed/19309347
236. Pariser, D. M., Lowe, N. J., Stewart, D. M., Jarratt, M. T., Lucky, A. W., Pariser, R. J., et.al. Photodynamic therapy with topical methyl aminolevulinate for actinic keratosis: results of a prospective randomized multicenter trial, J Am Acad Dermatol, 2003. 48(2): p. 227-32., https://www.ncbi.nlm.nih.gov/pubmed/12582393
237. Pariser, D., Loss, R., Jarratt, M., Abramovits, W., Spencer, J., Geronemus, R., et.al. Topical methyl-aminolevulinate photodynamic therapy using red light-emitting diode light for treatment of multiple actinic keratoses: A randomized, double-blind, placebo-controlled study, J Am Acad Dermatol, 2008. 59(4): p. 569-76., https://www.ncbi.nlm.nih.gov/pubmed/18707799
238. Tarstedt, M., Rosdahl, I., Berne, B., Svanberg, K., Wennberg, A. M., A randomized multicenter study to compare two treatment regimens of topical methyl aminolevulinate (Metvix)-PDT in actinic keratosis of the face and scalp, Acta Derm Venereol, 2005. 85(5): p. 424-8., https://www.ncbi.nlm.nih.gov/pubmed/16159735
239. von Felbert, V., Hoffmann, G., Hoff-Lesch, S., Abuzahra, F., Renn, C. N., Braathen, L. R., et.al. Photodynamic therapy of multiple actinic keratoses: reduced pain through use of visible light plus water-filtered infrared A compared with light from light-emitting diodes, Br J Dermatol, 2010. 163(3): p. 607-15., https://www.ncbi.nlm.nih.gov/pubmed/20426780
240. Seubring, I., Groenewoud, J. M. M., Gerritsen, M. P., Comparison of "Lesion-by-Lesion" and Field Photodynamic Therapy in the Prevention of Actinic Keratoses: A Randomized, Split-Face, Single-Blind Pilot Study, Dermatology, 2016. 232(6): p. 708-714., https://pubmed.ncbi.nlm.nih.gov/28095373/
241. Kohl, E., Popp, C., Zeman, F., Unger, P., Koller, M., Landthaler, M., et.al. Photodynamic therapy using intense pulsed light for treating actinic keratoses and photoaged skin of the dorsal hands: a randomized placebo-controlled study, Br J Dermatol, 2017. 176(2): p. 352-362., https://www.ncbi.nlm.nih.gov/pubmed/27518833
242. Hauschild, A, Stockfleth, E, Popp, G, Borrosch, F, Brüning, H, Dominicus, R, et.al. Optimization of photodynamic therapy with a novel self-adhesive 5-aminolaevulinic acid patch: results of two randomized controlled phase III studies., Br J Dermatol, 2009. 160 (5)(5): p. 1066-74., https://pubmed.ncbi.nlm.nih.gov/19222455/
243. Wiegell, S. R., Haedersdal, M., Philipsen, P. A., Eriksen, P., Enk, C. D., Wulf, H. C., Continuous activation of PpIX by daylight is as effective as and less painful than conventional photodynamic therapy for actinic keratoses; a randomized, controlled, single-blinded study, Br J Dermatol, 2008. 158(4): p. 740-6., https://www.ncbi.nlm.nih.gov/pubmed/18294318
244. Wiegell, S. R., Haedersdal, M., Eriksen, P., Wulf, H. C., Photodynamic therapy of actinic keratoses with 8% and 16% methyl aminolaevulinate and home-based daylight exposure: a double-blinded randomized clinical trial, Br J Dermatol, 2009. 160(6): p. 1308-14., https://www.ncbi.nlm.nih.gov/pubmed/19416257
245. Wiegell, S. R., Fabricius, S., Stender, I. M., Berne, B., Kroon, S., Andersen, B. L., et.al. A randomized, multicentre study of directed daylight exposure times of 1(1/2) vs. 2(1/2) h in daylight-mediated photodynamic therapy with methyl aminolaevulinate in patients with multiple thin actinic keratoses of the face and scalp, Br J Dermatol, 2011. 164(5): p. 1083-90., https://www.ncbi.nlm.nih.gov/pubmed/21219287
246. Neittaanmaki-Perttu, N., Gronroos, M., Karppinen, T., Snellman, E., Rissanen, P., Photodynamic Therapy for Actinic Keratoses: A Randomized Prospective Non-sponsored Cost-effectiveness Study of Daylight-mediated Treatment Compared with Light-emitting Diode Treatment, Acta Derm Venereol, 2016. 96(2): p. 241-4., https://www.ncbi.nlm.nih.gov/pubmed/26258496
247. Dirschka, T, Ekanayake-Bohlig, S, Dominicus, R, Aschoff, R, Herrera-Ceballos, E, Botella-Estrada, R, et.al. A randomized, intraindividual, non-inferiority, Phase III study comparing daylight photodynamic therapy with BF-200 ALA gel and MAL cream for the treatment of actinic keratosis., J Eur Acad Dermatol Venereol, 2019. 33 (2)(2): p. 288-297., https://pubmed.ncbi.nlm.nih.gov/30022544/
248. Rubel, D. M., Spelman, L., Murrell, D. F., See, J. A., Hewitt, D., Foley, P., et.al. Daylight photodynamic therapy with methyl aminolevulinate cream as a convenient, similarly effective, nearly painless alternative to conventional photodynamic therapy in actinic keratosis treatment: a randomized controlled trial, Br J Dermatol, 2014. 171(5): p. 1164-71., https://www.ncbi.nlm.nih.gov/pubmed/26258496
249. Lacour, J. P., Ulrich, C., Gilaberte, Y., Von Felbert, V., Basset-Seguin, N., Dreno, B., et.al. Daylight photodynamic therapy with methyl aminolevulinate cream is effective and nearly painless in treating actinic keratoses: a randomised, investigator-blinded, controlled, phase III study throughout Europe, J Eur Acad Dermatol Venereol, 2015. 29(12): p. 2342-8., https://www.ncbi.nlm.nih.gov/pubmed/26435363
250. Assikar, S, Labrunie, A, Kerob, D, Couraud, A, Bédane, C, Daylight photodynamic therapy with methyl aminolevulinate cream is as effective as conventional photodynamic therapy with blue light in the treatment of actinic keratosis: a controlled randomized intra-individual study., J Eur Acad Dermatol Venereol, 2020. 34 (8)(8): p. 1730-1735., https://pubmed.ncbi.nlm.nih.gov/31955461/
251. Räsänen, JE, Neittaanmäki, N, Ylitalo, L, Hagman, J, Rissanen, P, Ylianttila, L, et.al. 5-aminolaevulinic acid nanoemulsion is more effective than methyl-5-aminolaevulinate in daylight photodynamic therapy for actinic keratosis: a nonsponsored randomized double-blind multicentre trial., Br J Dermatol, 2019. 181 (2)(2): p. 265-274., https://pubmed.ncbi.nlm.nih.gov/30329163/
252. Dragieva, G., Prinz, B. M., Hafner, J., Dummer, R., Burg, G., Binswanger, U., et.al. A randomized controlled clinical trial of topical photodynamic therapy with methyl aminolaevulinate in the treatment of actinic keratoses in transplant recipients, Br J Dermatol, 2004. 151(1): p. 196-200., https://www.ncbi.nlm.nih.gov/pubmed/15270891
253. Morton, C, Horn, M, Leman, J, Tack, B, Bedane, C, Tjioe, M, et.al. Comparison of topical methyl aminolevulinate photodynamic therapy with cryotherapy or Fluorouracil for treatment of squamous cell carcinoma in situ: Results of a multicenter randomized trial., Arch Dermatol, 2006. 142 (6)(6): p. 729-35., https://pubmed.ncbi.nlm.nih.gov/16785375/
254. Miola, AC, Ferreira, ER, Lima, TRR, Schmitt, JV, Abbade, LPF, Miot, HA, Effectiveness and safety of 0·5% colchicine cream vs. photodynamic therapy with methyl aminolaevulinate in the treatment of actinic keratosis and skin field cancerization of the forearms: a randomized controlled trial., Br J Dermatol, 2018. 179 (5)(5): p. 1081-1087., https://pubmed.ncbi.nlm.nih.gov/29862491/
255. Ulrich, M, Reinhold, U, Dominicus, R, Aschoff, R, Szeimies, RM, Dirschka, T, Red light photodynamic therapy with BF-200 ALA showed superior efficacy in the treatment of actinic keratosis on the extremities, trunk, and neck in a vehicle-controlled phase III study., J Am Acad Dermatol, 2021. ():, https://pubmed.ncbi.nlm.nih.gov/33744350/
256. Brian Jiang, SI, Kempers, S, Rich, P, Marcus, S, Houlihan, A, Piacquadio, D, et.al. A Randomized, Vehicle-Controlled Phase 3 Study of Aminolevulinic Acid Photodynamic Therapy for the Treatment of Actinic Keratoses on the Upper Extremities., Dermatol Surg, 2019. 45 (7)(7): p. 890-897., https://pubmed.ncbi.nlm.nih.gov/30640777/
257. Ulrich, M, Reinhold, U, Dominicus, R, Aschoff, R, Szeimies, RM, Dirschka, T, Red light photodynamic therapy with BF-200 ALA showed superior efficacy in the treatment of actinic keratosis on the extremities, trunk, and neck in a vehicle-controlled phase III study., J Am Acad Dermatol, 2021. 85 (6)(6): p. 1510-1519., https://pubmed.ncbi.nlm.nih.gov/33744350/
258. Hauschild, A., Popp, G., Stockfleth, E., Meyer, K. G., Imberger, D., Mohr, P., et.al. Effective photodynamic therapy of actinic keratoses on the head and face with a novel, self-adhesive 5-aminolaevulinic acid patch, Exp Dermatol, 2009. 18(2): p. 116-21., https://www.ncbi.nlm.nih.gov/pubmed/18643849
259. Szeimies, R. M., Stockfleth, E., Popp, G., Borrosch, F., Bruning, H., Dominicus, R., et.al. Long-term follow-up of photodynamic therapy with a self-adhesive 5-aminolaevulinic acid patch: 12 months data, Br J Dermatol, 2010. 162(2): p. 410-4., https://www.ncbi.nlm.nih.gov/pubmed/19804593
260. Neittaanmaki-Perttu, N., Karppinen, T. T., Gronroos, M., Tani, T. T., Snellman, E., Daylight photodynamic therapy for actinic keratoses: a randomized double-blinded nonsponsored prospective study comparing 5-aminolaevulinic acid nanoemulsion (BF-200) with methyl-5-aminolaevulinate, Br J Dermatol, 2014. 171(5): p. 1172-80., https://www.ncbi.nlm.nih.gov/pubmed/25109244
261. Dahle, D. O., Grotmol, T., Leivestad, T., Hartmann, A., Midtvedt, K., Reisaeter, A. V., et.al. Association Between Pretransplant Cancer and Survival in Kidney Transplant Recipients, Transplantation, 2017. 101(10): p. 2599-2605., https://www.ncbi.nlm.nih.gov/pubmed/28207636
262. Togsverd-Bo, K, Halldin, C, Sandberg, C, Gonzalez, H, Wennberg, AM, Sørensen, SS, et.al. Photodynamic therapy is more effective than imiquimod for actinic keratosis in organ transplant recipients: a randomized intraindividual controlled trial., Br J Dermatol, 2018. 178 (4)(4): p. 903-909., https://pubmed.ncbi.nlm.nih.gov/28796885/
263. Veronese, F, Zavattaro, E, Orioni, G, Landucci, G, Tarantino, V, Airoldi, C, et.al. Efficacy of new class I medical device for actinic keratoses: a randomized controlled prospective study., J Dermatolog Treat, 2021. 32 (6)(6): p. 625-630., https://pubmed.ncbi.nlm.nih.gov/31689138/
264. Heppt, MV, Steeb, T, Niesert, AC, Zacher, M, Leiter, U, Garbe, C, et.al. Local interventions for actinic keratosis in organ transplant recipients: a systematic review., Br J Dermatol, 2019. 180 (1)(1): p. 43-50., https://pubmed.ncbi.nlm.nih.gov/30188570/
265. Wennberg, A. M., Stenquist, B., Stockfleth, E., Keohane, S., Lear, J. T., Jemec, G., et.al. Photodynamic therapy with methyl aminolevulinate for prevention of new skin lesions in transplant recipients: A randomized study, Transplantation, 2008. 86(3): p. 423-429., https://pubmed.ncbi.nlm.nih.gov/18698246/
266. Santos-Juanes, J., Esteve, A., Mas-Vidal, A., Coto-Segura, P., Salgueiro, E., Gomez, E., et.al. Acute renal failure caused by imiquimod 5% cream in a renal transplant patient: review of the literature on side effects of imiquimod, Dermatology, 2011. 222(2): p. 109-12., https://www.ncbi.nlm.nih.gov/pubmed/21304243
267. Akar, A., Bulent Tastan, H., Erbil, H., Arca, E., Kurumlu, Z., Gur, A. R., Efficacy and safety assessment of 0.5% and 1% colchicine cream in the treatment of actinic keratoses, J Dermatolog Treat, 2001. 12(4): p. 199-203., https://www.ncbi.nlm.nih.gov/pubmed/12241628
268. Alberts, D. S., Dorr, R. T., Einspahr, J. G., Aickin, M., Saboda, K., Xu, M. J., et.al. Chemoprevention of human actinic keratoses by topical 2-(difluoromethyl)-dl-ornithine, Cancer Epidemiol Biomarkers Prev, 2000. 9(12): p. 1281-6., https://www.ncbi.nlm.nih.gov/pubmed/11142412
269. Evans, M., Kalman, D., Alvarez, P., Paquet, M., Guthrie, N., A randomized, double-blind, placebo-controlled clinical trial evaluating Dermytol((R)) cream for the treatment of actinic keratoses, Clin Cosmet Investig Dermatol, 2014. 7: p. 215-24., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132222/
270. Moloney, F., Vestergaard, M., Radojkovic, B., Damian, D., Randomized, double-blinded, placebo controlled study to assess the effect of topical 1% nicotinamide on actinic keratoses, Br J Dermatol, 2010. 162(5): p. 1138-9., https://www.ncbi.nlm.nih.gov/pubmed/20199551
271. Pflugfelder, A., Andonov, E., Weide, B., Dirschka, T., Schempp, C., Stockfleth, E., et.al. Lack of activity of betulin-based Oleogel-S10 in the treatment of actinic keratoses: a randomized, multicentre, placebo-controlled double-blind phase II trial, Br J Dermatol, 2015. 172(4): p. 926-32., https://www.ncbi.nlm.nih.gov/pubmed/25124939/
272. Tong, D. W., Barnetson, R. S., Beta-1,3-D-glucan gel in the treatment of solar keratoses, Australas J Dermatol, 1996. 37(3): p. 137-8., https://www.ncbi.nlm.nih.gov/pubmed/8771866
273. Thompson, S. C., Jolley, D., Marks, R., Reduction of solar keratoses by regular sunscreen use, N Engl J Med, 1993. 329(16): p. 1147-51., https://www.ncbi.nlm.nih.gov/pubmed/8377777
274. Stoddard, M, Herrmann, J, Moy, L, Moy, R, Improvement of Actinic Keratoses Using Topical DNA Repair Enzymes: A Randomized Placebo-Controlled Trial., J Drugs Dermatol, 2017. 16 (10)(10): p. 1030-1034., https://pubmed.ncbi.nlm.nih.gov/29036257/
275. Yang, CC, Wong, TW, Lee, CH, Hong, CH, Chang, CH, Lai, FJ, et.al. Efficacy and safety of topical SR-T100 gel in treating actinic keratosis in Taiwan: A Phase III randomized double-blind vehicle-controlled parallel trial., J Dermatol Sci, 2018. 90 (3)(3): p. 295-302., https://pubmed.ncbi.nlm.nih.gov/29530340/
276. Weiss, J., Ulrich, M., Bukhalo, M., Osterdal, M. L., Bang, B., Hanke, C. W., A seamless phase I/II dose-finding trial assessing ingenol disoxate (LEO 43204) for field treatment of actinic keratosis on the scalp, Br J Dermatol, 2017. 176(6): p. 1456-1464., https://www.ncbi.nlm.nih.gov/pubmed/28078678
277. Bourcier, M., Stein Gold, L., Guenther, L., Andreassen, C. M., Selmer, J., Goldenberg, G., A dose-finding trial with a novel ingenol derivative (ingenol disoxate: LEO 43204) for field treatment of actinic keratosis on full face or 250 cm2 on the chest, J Dermatolog Treat, 2017. p. 1-7., https://www.ncbi.nlm.nih.gov/pubmed/28264612
278. Szeimies, R. M., Bichel, J., Ortonne, J. P., Stockfleth, E., Lee, J., Meng, T. C., A phase II dose-ranging study of topical resiquimod to treat actinic keratosis, Br J Dermatol, 2008. 159(1): p. 205-10., https://www.ncbi.nlm.nih.gov/pubmed/18476957
279. Huyke, C., Laszczyk, M., Scheffler, A., Ernst, R., Schempp, C. M., [Treatment of actinic keratoses with birch bark extract: a pilot study], J Dtsch Dermatol Ges, 2006. 4(2): p. 132-6., https://www.ncbi.nlm.nih.gov/pubmed/16503940
280. Huyke, C., Reuter, J., Rodig, M., Kersten, A., Laszczyk, M., Scheffler, A., et.al. Treatment of actinic keratoses with a novel betulin-based oleogel. A prospective, randomized, comparative pilot study, J Dtsch Dermatol Ges, 2009. 7(2): p. 128-33., https://www.ncbi.nlm.nih.gov/pubmed/18808378
281. Jurk, M., Heil, F., Vollmer, J., Schetter, C., Krieg, A. M., Wagner, H., et.al. Human TLR7 or TLR8 independently confer responsiveness to the antiviral compound R-848, Nat Immunol, 2002. 3(6): p. 499., https://www.ncbi.nlm.nih.gov/pubmed/12032557
282. Alirezai, M., Dupuy, P., Amblard, P., Kalis, B., Souteyrand, P., Frappaz, A., et.al. Clinical evaluation of topical isotretinoin in the treatment of actinic keratoses, J Am Acad Dermatol, 1994. 30(3): p. 447-51., https://www.ncbi.nlm.nih.gov/pubmed/8113458
283. Misiewicz, J., Sendagorta, E., Golebiowska, A., Lorenc, B., Czarnetzki, B. M., Jablonska, S., Topical treatment of multiple actinic keratoses of the face with arotinoid methyl sulfone (Ro 14-9706) cream versus tretinoin cream: a double-blind, comparative study, J Am Acad Dermatol, 1991. 24(3): p. 448-51., https://www.ncbi.nlm.nih.gov/pubmed/2061443
284. Kang, S., Goldfarb, M. T., Weiss, J. S., Metz, R. D., Hamilton, T. A., Voorhees, J. J., et.al. Assessment of adapalene gel for the treatment of actinic keratoses and lentigines: a randomized trial, J Am Acad Dermatol, 2003. 49(1): p. 83-90., https://www.ncbi.nlm.nih.gov/pubmed/12833014
285. Moriarty, M., Dunn, J., Darragh, A., Lambe, R., Brick, I., Etretinate in treatment of actinic keratosis. A double-blind crossover study, Lancet, 1982. 1(8268): p. 364-5., https://www.ncbi.nlm.nih.gov/pubmed/6120350
286. Amann, P. M., Merk, H. F., Baron, J. M., [Retinoids in dermatopharmacology], Hautarzt, 2014. 65(2): p. 98-105., https://www.ncbi.nlm.nih.gov/pubmed/24419474
287. Chen, K., Craig, J. C., Shumack, S., Oral retinoids for the prevention of skin cancers in solid organ transplant recipients: a systematic review of randomized controlled trials, Br J Dermatol, 2005. 152(3): p. 518-23., https://www.ncbi.nlm.nih.gov/pubmed/15787821
288. Watson, A. B., Preventative effect of etretinate therapy on multiple actinic keratoses, Cancer Detect Prev, 1986. 9(1-2): p. 161-5., https://www.ncbi.nlm.nih.gov/pubmed/3524840
289. Bercovitch, L., Topical chemotherapy of actinic keratoses of the upper extremity with tretinoin and 5-fluorouracil: a double-blind controlled study, Br J Dermatol, 1987. 116(4): p. 549-52., https://www.ncbi.nlm.nih.gov/pubmed/3555597
290. Robinson, JK, Actinic cheilitis. A prospective study comparing four treatment methods., Arch Otolaryngol Head Neck Surg, 1989. 115 (7)(7): p. 848-52., https://pubmed.ncbi.nlm.nih.gov/2736096/
291. Lai, M, Pampena, R, Cornacchia, L, Pellacani, G, Peris, K, Longo, C, Treatments of actinic cheilitis: A systematic review of the literature., J Am Acad Dermatol, 2020. 83 (3)(3): p. 876-887., https://pubmed.ncbi.nlm.nih.gov/31400450/
292. Carvalho, MV, de Moraes, SLD, Lemos, CAA, Santiago Júnior, JF, Vasconcelos, BCDE, Pellizzer, EP, Surgical versus non-surgical treatment of actinic cheilitis: A systematic review and meta-analysis., Oral Dis, 2019. 25 (4)(4): p. 972-981., https://pubmed.ncbi.nlm.nih.gov/29908101/
293. Salgueiro, AP, de Jesus, LH, de Souza, IF, Rados, PV, Visioli, F, Treatment of actinic cheilitis: a systematic review., Clin Oral Investig, 2019. 23 (5)(5): p. 2041-2053., https://pubmed.ncbi.nlm.nih.gov/31011833/
294. Laws, RA, Wilde, JL, Grabski, WJ, Comparison of electrodessication with CO2 laser for the treatment of actinic cheilitis., Dermatol Surg, 2000. 26 (4)(4): p. 349-53., https://pubmed.ncbi.nlm.nih.gov/10759824/
295. Lubritz, RR, Smolewski, SA, Cryosurgery cure rate of premalignant leukoplakia of the lower lip., J Dermatol Surg Oncol, 1983. 9 (3)(3): p. 235-7., https://pubmed.ncbi.nlm.nih.gov/6826879/
296. Shah, AY, Doherty, SD, Rosen, T, Actinic cheilitis: a treatment review., Int J Dermatol, 2010. 49 (11)(11): p. 1225-34., https://pubmed.ncbi.nlm.nih.gov/20964646/
297. Alamillos-Granados, FJ, Naval-Gías, L, Dean-Ferrer, A, Alonso del Hoyo, JR, Carbon dioxide laser vermilionectomy for actinic cheilitis., J Oral Maxillofac Surg, 1993. 51 (2)(2): p. 118-21., https://pubmed.ncbi.nlm.nih.gov/8426249/
298. Dufresne, RG, Garrett, AB, Bailin, PL, Ratz, JL, Carbon dioxide laser treatment of chronic actinic cheilitis., J Am Acad Dermatol, 1988. 19 (5 Pt 1)(5 Pt 1): p. 876-8., https://pubmed.ncbi.nlm.nih.gov/3142939/
299. Castiñeiras, I, Del Pozo, J, Mazaira, M, Rodríguez-Lojo, R, Fonseca, E, Actinic cheilitis: evolution to squamous cell carcinoma after carbon dioxide laser vaporization. A study of 43 cases., J Dermatolog Treat, 2010. 21 (1)(1): p. 49-53., https://pubmed.ncbi.nlm.nih.gov/19418331/
300. Orenstein, A, Goldan, O, Weissman, O, Winkler, E, Haik, J, A new modality in the treatment of actinic cheilitis using the Er:YAG laser., J Cosmet Laser Ther, 2007. 9 (1)(1): p. 23-5., https://pubmed.ncbi.nlm.nih.gov/17506137/
301. Gonzaga, AKG, de Oliveira, PT, da Silveira, ÉJD, Queiroz, LMG, de Medeiros, AMC, Diclofenac sodium gel therapy as an alternative to actinic cheilitis., Clin Oral Investig, 2018. 22 (3)(3): p. 1319-1325., https://pubmed.ncbi.nlm.nih.gov/28986686/
302. Husein-ElAhmed, H, Almazan-Fernandez, FM, Husein-ElAhmed, S, Ingenol mebutate versus imiquimod versus diclofenac for actinic cheilitis: a 6-month follow-up clinical study., Clin Exp Dermatol, 2019. 44 (2)(2): p. 231-234., https://pubmed.ncbi.nlm.nih.gov/30242791/
303. Lima, Gda S, Silva, GF, Gomes, AP, de Araújo, LM, Salum, FG, Diclofenac in hyaluronic acid gel: an alternative treatment for actinic cheilitis., J Appl Oral Sci 18 (5)(5): p. 533-7., https://pubmed.ncbi.nlm.nih.gov/21085813/
304. Smith, KJ, Germain, M, Yeager, J, Skelton, H, Topical 5% imiquimod for the therapy of actinic cheilitis., J Am Acad Dermatol, 2002. 47 (4)(4): p. 497-501., https://pubmed.ncbi.nlm.nih.gov/12271290/
305. Paolino, G, Cantoresi, F, Mercuri, SR, Cantisani, C, Clinical evaluation and efficacy of Imiquimod 3.75% cream for the treatment of actinic keratosis, pigmented basal cell carcinomas, and actinic cheilitis., Dermatol Ther, 2020. 33 (3)(3): p. e13356., https://pubmed.ncbi.nlm.nih.gov/32239714/
306. Sotiriou, E, Apalla, Z, Koussidou-Erremonti, T, Ioannides, D, Actinic cheilitis treated with one cycle of 5-aminolaevulinic acid-based photodynamic therapy: report of 10 cases., Br J Dermatol, 2008. 159 (1)(1): p. 261-2., https://pubmed.ncbi.nlm.nih.gov/18489592/
307. Sotiriou, E, Apalla, Z, Chovarda, E, Panagiotidou, D, Ioannides, D, Photodynamic therapy with 5-aminolevulinic acid in actinic cheilitis: an 18-month clinical and histological follow-up., J Eur Acad Dermatol Venereol, 2010. 24 (8)(8): p. 916-20., https://pubmed.ncbi.nlm.nih.gov/20028448/
308. Berking, C, Herzinger, T, Flaig, MJ, Brenner, M, Borelli, C, Degitz, K, The efficacy of photodynamic therapy in actinic cheilitis of the lower lip: a prospective study of 15 patients., Dermatol Surg, 2007. 33 (7)(7): p. 825-30., https://pubmed.ncbi.nlm.nih.gov/17598848/
309. Chaves, YN, Torezan, LA, Lourenço, SV, Neto, CF, Evaluation of the efficacy of photodynamic therapy for the treatment of actinic cheilitis., Photodermatol Photoimmunol Photomed, 2017. 33 (1)(1): p. 14-21., https://pubmed.ncbi.nlm.nih.gov/27864997/
310. Ribeiro, CF, Souza, FH, Jordão, JM, Haendchen, LC, Mesquita, L, Schmitt, JV, et.al. Photodynamic therapy in actinic cheilitis: clinical and anatomopathological evaluation of 19 patients., An Bras Dermatol 87 (3)(3): p. 418-23., https://pubmed.ncbi.nlm.nih.gov/22714758/
311. Radakovic, S, Tanew, A, 5-aminolaevulinic acid patch-photodynamic therapy in the treatment of actinic cheilitis., Photodermatol Photoimmunol Photomed, 2017. 33 (6)(6): p. 306-310., https://pubmed.ncbi.nlm.nih.gov/28703320/
312. Radakovic, S, Dangl, M, Tanew, A, 5-Aminolevulinic acid patch (Alacare) photodynamic therapy for actinic cheilitis: data from a prospective 12-month follow-up study on 21 patients., J Eur Acad Dermatol Venereol, 2020. 34 (9)(9): p. 2011-2015., https://pubmed.ncbi.nlm.nih.gov/31999856/
313. Yazdani Abyaneh, MA, Falto-Aizpurua, L, Griffith, RD, Nouri, K, Photodynamic therapy for actinic cheilitis: a systematic review., Dermatol Surg, 2015. 41 (2)(2): p. 189-98., https://pubmed.ncbi.nlm.nih.gov/25627629/
314. Levi, A, Hodak, E, Enk, CD, Snast, I, Slodownik, D, Lapidoth, M, Daylight photodynamic therapy for the treatment of actinic cheilitis., Photodermatol Photoimmunol Photomed, 2019. 35 (1)(1): p. 11-16., https://pubmed.ncbi.nlm.nih.gov/30066408/
315. Andreadis, D, Pavlou, A-, Vakirlis, E, Anagnostou, E, Vrani, F, Poulopoulos, A, et.al. Daylight photodynamic therapy for the management of actinic cheilitis., Arch Dermatol Res, 2020. 312 (10)(10): p. 731-737., https://pubmed.ncbi.nlm.nih.gov/32266532/
316. Choi, SH, Kim, KH, Song, KH, Efficacy of ablative fractional laser-assisted photodynamic therapy for the treatment of actinic cheilitis: 12-month follow-up results of a prospective, randomized, comparative trial., Br J Dermatol, 2015. 173 (1)(1): p. 184-91., https://pubmed.ncbi.nlm.nih.gov/25400009/
317. Sotiriou, E, Lallas, A, Goussi, C, Apalla, Z, Trigoni, A, Chovarda, E, et.al. Sequential use of photodynamic therapy and imiquimod 5% cream for the treatment of actinic cheilitis: a 12-month follow-up study., Br J Dermatol, 2011. 165 (4)(4): p. 888-92., https://pubmed.ncbi.nlm.nih.gov/21916880/
318. Ali, H, Shipman, AR, Orpin, SD, John Templeton Bowen, MD, 1857-1940: the centenary of his most famous publication., Clin Exp Dermatol, 2012. 37 (7)(7): p. 825-8., https://pubmed.ncbi.nlm.nih.gov/22998547/
319. Peterka, ES, Lynch, FW, Goltz, RW, An association between Bowen's disease and internal cancer., Arch Dermatol, 1961. 84 (4): p. 623 - 629., https://pubmed.ncbi.nlm.nih.gov/14485715/
320. Kao, GF, Carcinoma arising in Bowen's disease., Arch Dermatol, 1986. 122 (10)(10): p. 1124-6., https://pubmed.ncbi.nlm.nih.gov/3767398/
321. Leibovitch, I, Huilgol, SC, Selva, D, Richards, S, Paver, R, Cutaneous squamous carcinoma in situ (Bowen's disease): treatment with Mohs micrographic surgery., J Am Acad Dermatol, 2005. 52 (6)(6): p. 997-1002., https://pubmed.ncbi.nlm.nih.gov/15928618/
322. Morton, CA, Whitehurst, C, Moseley, H, McColl, JH, Moore, JV, Mackie, RM, Comparison of photodynamic therapy with cryotherapy in the treatment of Bowen's disease., Br J Dermatol, 1996. 135 (5)(5): p. 766-71., https://pubmed.ncbi.nlm.nih.gov/8977678/
323. Bath-Hextall, FJ, Matin, RN, Wilkinson, D, Leonardi-Bee, J, Interventions for cutaneous Bowen's disease., Cochrane Database Syst Rev, 2013. (6)(6): p. CD007281., https://pubmed.ncbi.nlm.nih.gov/23794286/
324. Cai, H, Wang, YX, Zheng, JC, Sun, P, Yang, ZY, Li, YL, et.al. Photodynamic therapy in combination with CO2 laser for the treatment of Bowen's disease., Lasers Med Sci, 2015. 30 (5)(5): p. 1505-10., https://pubmed.ncbi.nlm.nih.gov/25899562/
325. Perrett, CM, McGregor, JM, Warwick, J, Karran, P, Leigh, IM, Proby, CM, et.al. Treatment of post-transplant premalignant skin disease: a randomized intrapatient comparative study of 5-fluorouracil cream and topical photodynamic therapy., Br J Dermatol, 2007. 156 (2)(2): p. 320-8., https://pubmed.ncbi.nlm.nih.gov/17223873/
326. Salim, A, Leman, JA, McColl, JH, Chapman, R, Morton, CA, Randomized comparison of photodynamic therapy with topical 5-fluorouracil in Bowen's disease., Br J Dermatol, 2003. 148 (3)(3): p. 539-43., https://pubmed.ncbi.nlm.nih.gov/12653747/
327. Patel, GK, Goodwin, R, Chawla, M, Laidler, P, Price, PE, Finlay, AY, et.al. Imiquimod 5% cream monotherapy for cutaneous squamous cell carcinoma in situ (Bowen's disease): a randomized, double-blind, placebo-controlled trial., J Am Acad Dermatol, 2006. 54 (6)(6): p. 1025-32., https://pubmed.ncbi.nlm.nih.gov/16713457/
328. Morton, CA, Whitehurst, C, Moore, JV, MacKie, RM, Comparison of red and green light in the treatment of Bowen's disease by photodynamic therapy., Br J Dermatol, 2000. 143 (4)(4): p. 767-72., https://pubmed.ncbi.nlm.nih.gov/11069454/
329. Genouw, E, Verheire, B, Ongenae, K, De Schepper, S, Creytens, D, Verhaeghe, E, et.al. Laser-assisted photodynamic therapy for superficial basal cell carcinoma and Bowen's disease: a randomized intrapatient comparison between a continuous and a fractional ablative CO, J Eur Acad Dermatol Venereol, 2018. 32 (11)(11): p. 1897-1905., https://pubmed.ncbi.nlm.nih.gov/29633367/
330. Kim, HJ, Song, KH, Ablative fractional laser-assisted photodynamic therapy provides superior long-term efficacy compared with standard methyl aminolevulinate photodynamic therapy for lower extremity Bowen disease., J Am Acad Dermatol, 2018. 79 (5)(5): p. 860-868., https://pubmed.ncbi.nlm.nih.gov/29857012/
331. Ko, DY, Kim, KH, Song, KH, A randomized trial comparing methyl aminolaevulinate photodynamic therapy with and without Er:YAG ablative fractional laser treatment in Asian patients with lower extremity Bowen disease: results from a 12-month follow-up., Br J Dermatol, 2014. 170 (1)(1): p. 165-72., https://pubmed.ncbi.nlm.nih.gov/24102369/
332. Wu, Y, Wang, P, Zhang, L, Wang, B, Wang, X, Enhancement of Photodynamic Therapy for Bowen's Disease Using Plum-Blossom Needling to Augment Drug Delivery., Dermatol Surg, 2018. 44 (12)(12): p. 1516-1524., https://pubmed.ncbi.nlm.nih.gov/29994952/
333. Sun, L, Chin, RI, Gastman, B, Thorstad, W, Yom, SS, Reddy, CA, et.al. Association of Disease Recurrence With Survival Outcomes in Patients With Cutaneous Squamous Cell Carcinoma of the Head and Neck Treated With Multimodality Therapy., JAMA Dermatol, 2019. 155 (4)(4): p. 442-447., https://pubmed.ncbi.nlm.nih.gov/30810715/
334. Breuninger, H., Schaumburg-Lever, G., Holzschuh, J., Horny, H. P., Desmoplastic squamous cell carcinoma of skin and vermilion surface: a highly malignant subtype of skin cancer, Cancer, 1997. 79(5): p. 915-9., https://www.ncbi.nlm.nih.gov/pubmed/9041153
335. Clayman, G. L., Lee, J. J., Holsinger, F. C., Zhou, X., Duvic, M., El-Naggar, A. K., et.al. Mortality risk from squamous cell skin cancer, J Clin Oncol, 2005. 23(4): p. 759-65., https://www.ncbi.nlm.nih.gov/pubmed/15681519
336. Tschetter, AJ, Campoli, MR, Zitelli, JA, Brodland, DG, Long-term clinical outcomes of patients with invasive cutaneous squamous cell carcinoma treated with Mohs micrographic surgery: A 5-year, multicenter, prospective cohort study., J Am Acad Dermatol, 2020. 82 (1)(1): p. 139-148., https://pubmed.ncbi.nlm.nih.gov/31279037/
337. Dzubow, L. M., Rigel, D. S., Robins, P., Risk factors for local recurrence of primary cutaneous squamous cell carcinomas. Treatment by microscopically controlled excision, Arch Dermatol, 1982. 118(11): p. 900-2., https://www.ncbi.nlm.nih.gov/pubmed/7138046
338. Breuninger, H., Black, B., Rassner, G., Microstaging of squamous cell carcinomas, Am J Clin Pathol, 1990. 94(5): p. 624-7., https://www.ncbi.nlm.nih.gov/pubmed/2239827
339. Eroglu, A., Berberoglu, U., Berreroglu, S., Risk factors related to locoregional recurrence in squamous cell carcinoma of the skin, J Surg Oncol, 1996. 61(2): p. 124-30., https://pubmed.ncbi.nlm.nih.gov/8606543/
340. Mourouzis, C., Boynton, A., Grant, J., Umar, T., Wilson, A., Macpheson, D., et.al. Cutaneous head and neck SCCs and risk of nodal metastasis - UK experience, J Craniomaxillofac Surg, 2009. 37(8): p. 443-7., https://www.ncbi.nlm.nih.gov/pubmed/19713116
341. Brougham, N. D., Dennett, E. R., Cameron, R., Tan, S. T., The incidence of metastasis from cutaneous squamous cell carcinoma and the impact of its risk factors, J Surg Oncol, 2012. 106(7): p. 811-5., https://www.ncbi.nlm.nih.gov/pubmed/22592943
342. Peat, B., Insull, P., Ayers, R., Risk stratification for metastasis from cutaneous squamous cell carcinoma of the head and neck, ANZ J Surg, 2012. 82(4): p. 230-3., https://www.ncbi.nlm.nih.gov/pubmed/22510179
343. Karia, P. S., Jambusaria-Pahlajani, A., Harrington, D. P., Murphy, G. F., Qureshi, A. A., Schmults, C. D., Evaluation of American Joint Committee on Cancer, International Union Against Cancer, and Brigham and Women's Hospital tumor staging for cutaneous squamous cell carcinoma, J Clin Oncol, 2014. 32(4): p. 327-34., https://www.ncbi.nlm.nih.gov/pubmed/24366933
344. Vasconcelos, L., Melo, J. C., Miot, H. A., Marques, M. E., Abbade, L. P., Invasive head and neck cutaneous squamous cell carcinoma: clinical and histopathological characteristics, frequency of local recurrence and metastasis, An Bras Dermatol, 2014. 89(4): p. 562-8., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148268/pdf/abd-89-04-0562.pdf
345. Wermker, K., Belok, F., Schipmann, S., Klein, M., Schulze, H. J., Hallermann, C., Prediction model for lymph node metastasis and recommendations for elective neck dissection in lip cancer, J Craniomaxillofac Surg, 2015. 43(4): p. 545-52., https://www.ncbi.nlm.nih.gov/pubmed/25753473
346. Harris, B. N., Bayoumi, A., Rao, S., Moore, M. G., Farwell, D. G., Bewley, A. F., Factors Associated with Recurrence and Regional Adenopathy for Head and Neck Cutaneous Squamous Cell Carcinoma, Otolaryngol Head Neck Surg, 2017. 156(5): p. 863-869., http://journals.sagepub.com/doi/pdf/10.1177/0194599817697053
347. Khan, K, Mykula, R, Kerstein, R, Rabey, N, Bragg, T, Crick, A, et.al. A 5-year follow-up study of 633 cutaneous SCC excisions: Rates of local recurrence and lymph node metastasis., J Plast Reconstr Aesthet Surg, 2018. 71 (8)(8): p. 1153-1158., https://pubmed.ncbi.nlm.nih.gov/29803777/
348. Stewart, TJ, Saunders, A, Risk factors for positive margins after wide local excision of cutaneous squamous cell carcinoma., J Dermatolog Treat, 2018. 29 (7)(7): p. 706-708., https://pubmed.ncbi.nlm.nih.gov/29448853/
349. van Lee, CB, Roorda, BM, Wakkee, M, Voorham, Q, Mooyaart, AL, de Vijlder, HC, et.al. Recurrence rates of cutaneous squamous cell carcinoma of the head and neck after Mohs micrographic surgery vs. standard excision: a retrospective cohort study., Br J Dermatol, 2019. 181 (2)(2): p. 338-343., https://pubmed.ncbi.nlm.nih.gov/30199574/
350. Korhonen, N, Ylitalo, L, Luukkaala, T, Itkonen, J, Häihälä, H, Jernman, J, et.al. Recurrent and Metastatic Cutaneous Squamous Cell Carcinomas in a Cohort of 774 Patients in Finland., Acta Derm Venereol, 2020. 100 (8)(8): p. adv00121., https://pubmed.ncbi.nlm.nih.gov/32255495/
351. Rowe, D. E., Carroll, R. J., Day, C. L., Jr., Prognostic factors for local recurrence, metastasis, and survival rates in squamous cell carcinoma of the skin, ear, and lip. Implications for treatment modality selection, J Am Acad Dermatol, 1992. 26(6): p. 976-90., https://www.ncbi.nlm.nih.gov/pubmed/1607418
352. Alam , Murad, Ratner , Désirée, Cutaneous Squamous-Cell Carcinoma, New England Journal of Medicine, 2001. 344(13): p. 975-983., http://www.nejm.org/doi/full/10.1056/NEJM200103293441306
353. Cheng, J., Yan, S., Prognostic variables in high-risk cutaneous squamous cell carcinoma: a review, J Cutan Pathol, 2016. 43(11): p. 994-1004., http://onlinelibrary.wiley.com/store/10.1111/cup.12766/asset/cup12766.pdf?v=1&t=j9zgbtpz&s=3c3898fa72baae8ce9a31a08d090a8acc21f740f
354. Skulsky, S. L., O'Sullivan, B., McArdle, O., Leader, M., Roche, M., Conlon, P. J., et.al. Review of high-risk features of cutaneous squamous cell carcinoma and discrepancies between the American Joint Committee on Cancer and NCCN Clinical Practice Guidelines In Oncology, Head Neck, 2017. 39(3): p. 578-594., https://pubmed.ncbi.nlm.nih.gov/27882625/
355. Johnson, TM, Smith, NR, Mohs Surgery versus Standard Local Excision for Basal Cell Carcinoma, Squamous Cell Carcinoma, and Melanoma Skin Cancer., Facial Plast Surg, 2020. 36 (2)(2): p. 133-140., https://pubmed.ncbi.nlm.nih.gov/32413920/
356. Breuninger, H, Eigentler, T, Häfner, HM, Leiter, U, Local surgical treatment of cutaneous squamous cell carcinoma: deficits and controversies in the literature., J Dtsch Dermatol Ges, 2019. 17 (10)(10): p. 999-1004., https://pubmed.ncbi.nlm.nih.gov/31545559/
357. Breuninger, H., Brantsch, K., Eigentler, T., Häfner, H.-M., Comparison and evaluation of the current staging of cutaneous carcinomas, JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2012. 10(8): p. 579-586., http://dx.doi.org/10.1111/j.1610-0387.2012.07896.x
358. Roscher, I, Falk, RS, Vos, L, Clausen, OPF, Helsing, P, Gjersvik, P, et.al. Validating 4 Staging Systems for Cutaneous Squamous Cell Carcinoma Using Population-Based Data: A Nested Case-Control Study., JAMA Dermatol, 2018. 154 (4)(4): p. 428-434., https://pubmed.ncbi.nlm.nih.gov/29516080/
359. Stratigos, AJ, Garbe, C, Dessinioti, C, Lebbe, C, Bataille, V, Bastholt, L, et.al. European interdisciplinary guideline on invasive squamous cell carcinoma of the skin: Part 1. epidemiology, diagnostics and prevention., Eur J Cancer, 2020. 128 (): p. 60-82., https://pubmed.ncbi.nlm.nih.gov/32113941/
360. Bonerandi, J. J., Beauvillain, C., Caquant, L., Chassagne, J. F., Chaussade, V., Clavere, P., et.al. Guidelines for the diagnosis and treatment of cutaneous squamous cell carcinoma and precursor lesions, J Eur Acad Dermatol Venereol, 2011. 25 Suppl 5: p. 1-51., https://www.ncbi.nlm.nih.gov/pubmed/22070399
361. SIGN, Scottish Intercollegiate Guidelines Network (SIGN). Management of primary cutaneous squamous cell carcinoma. Edinburgh: SIGN; 2014. (SIGN publication no. 140). [June 2014], http://www.sign.ac.uk Last access November 2017, 2014., https://www.sign.ac.uk/sign-140-management-of-primary-cutaneous-squamous-cell-carcinoma.html
362. Breuninger, Helmut, Eigentler, Thomas, Bootz, Friedrich, Hauschild, Axel, Kortmann, Rolf-Dieter, Wolff, Klaus, et.al. Brief S2k guidelines – Cutaneous squamous cell carcinoma, JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2013. 11(s3): p. 37-45., http://dx.doi.org/10.1111/ddg.12015_7
363. Schweinzer K, et al., Different characteristics between common and desmoplastic cutaneous SCC in local infiltration and local recurrence, Not yet published
364. Schweinzer, K., Kofler, L., Bauer, J., Metzler, G., Breuninger, H., Hafner, H. M., Cytokeratin AE1/AE3 immunostaining and 3D-histology: improvement of diagnosis in desmoplastic squamous cell carcinoma of the skin, Arch Dermatol Res, 2017. 309(1): p. 43-46., https://www.ncbi.nlm.nih.gov/pubmed/27864629
365. Erkan, Serkan, Savundra, James M., Wood, Bradley, Acharya, Aanand N., Rajan, Gunesh P., Clinical perineural invasion of the trigeminal and facial nerves in cutaneous head and neck squamous cell carcinoma: Outcomes and prognostic implications of multimodality and salvage treatment, Head & Neck, 2017. 39(7): p. 1280-1286., https://onlinelibrary.wiley.com/doi/abs/10.1002/hed.24607
366. Warren, T. A., Panizza, B., Porceddu, S. V., Gandhi, M., Patel, P., Wood, M., et.al. Outcomes after surgery and postoperative radiotherapy for perineural spread of head and neck cutaneous squamous cell carcinoma, Head Neck, 2016. 38(6): p. 824-31., https://www.ncbi.nlm.nih.gov/pubmed/25546817
367. Hutting, K. H., Bos, P. G., Kibbelaar, R. E., Veeger, Njgm, Marck, K. W., Moues, C. M., Effective excision of cutaneous squamous cell carcinoma of the face using analysis of intra-operative frozen sections from the whole specimen, J Surg Oncol, 2017., https://www.ncbi.nlm.nih.gov/pubmed/29073717
368. Jambusaria-Pahlajani, A., Miller, C. J., Quon, H., Smith, N., Klein, R. Q., Schmults, C. D., Surgical monotherapy versus surgery plus adjuvant radiotherapy in high-risk cutaneous squamous cell carcinoma: a systematic review of outcomes, Dermatol Surg, 2009. 35(4): p. 574-85., https://pubmed.ncbi.nlm.nih.gov/19415791/
369. Turner, R. J., Leonard, N., Malcolm, A. J., Lawrence, C. M., Dahl, M. G., A retrospective study of outcome of Mohs' micrographic surgery for cutaneous squamous cell carcinoma using formalin fixed sections, Br J Dermatol, 2000. 142(4): p. 752-7., https://www.ncbi.nlm.nih.gov/pubmed/10792227
370. Dunn, M., Morgan, M. B., Beer, T. W., Perineural invasion: identification, significance, and a standardized definition, Dermatol Surg, 2009. 35(2): p. 214-21., http://onlinelibrary.wiley.com/store/10.1111/j.1524-4725.2008.34412.x/asset/j.1524-4725.2008.34412.x.pdf?v=1&t=j9zgnt7q&s=a63f0e26d61e2e8825c3d0e039505b37ae0177c4
371. Haug, K, Breuninger, H, Metzler, G, Eigentler, T, Eichner, M, Häfner, HM, et.al. Prognostic Impact of Perineural Invasion in Cutaneous Squamous Cell Carcinoma: Results of a Prospective Study of 1,399 Tumors., J Invest Dermatol, 2020. 140 (10)(10): p. 1968-1975., https://pubmed.ncbi.nlm.nih.gov/32169476/
372. Freeman, Robert G., Knox, John M., Heaton, Charles L., The treatment of skin cancer. A statistical study of 1,341 skin tumors comparing results obtained with irradiation, surgery, and curettage followed by electrodesiccation, Cancer, 1964. 17(4): p. 535-538., https://www.ncbi.nlm.nih.gov/pubmed/14136537
373. Zitelli, JA, Secondary intention healing: an alternative to surgical repair., Clin Dermatol 2 (3)(3): p. 92-106., https://pubmed.ncbi.nlm.nih.gov/6400321/
374. Bechara, FG, [Healing by secondary intention after skin cancer surgery on the head and neck]., Hautarzt, 2013. 64 (8)(8): p. 567-76., https://pubmed.ncbi.nlm.nih.gov/23868572/
375. Swetter, SM, Boldrick, JC, Pierre, P, Wong, P, Egbert, BM, Effects of biopsy-induced wound healing on residual basal cell and squamous cell carcinomas: rate of tumor regression in excisional specimens., J Cutan Pathol, 2003. 30 (2)(2): p. 139-46., https://pubmed.ncbi.nlm.nih.gov/12641794/
376. Grupp, M, Illes, M, Mentzel, J, Simon, JC, Paasch, U, Grunewald, S, Schnittrandkontrolle von Basalzellkarzinomen mittels ex-vivo konfokaler Laserscanmikroskopie mit digitaler Farbbearbeitung - Anwendung in der Routinediagnostik, J Dtsch Dermatol Ges, 2021. 19 (5)(5): p. 685-693., https://pubmed.ncbi.nlm.nih.gov/33979047/
377. Peters, N, Schubert, M, Bauer, J, Ghoreschi, FC, Moehrle, M, Rapid Lump Examination (RLE) - eine schnelle Methode in der mikroskopisch kontrollierten Chirurgie von Basalzellkarzinomen, J Dtsch Dermatol Ges, 2019. 17 (11)(11): p. 1131-1140., https://pubmed.ncbi.nlm.nih.gov/31765084/
378. Eberle, FC, Kanyildiz, M, Schnabl, SM, Schulz, C, Häfner, HM, Adam, P, et.al. Three dimensional (3D) histology in daily routine: practical implementation and its evaluation., J Dtsch Dermatol Ges, 2014. 12 (11)(11): p. 1028-35., https://pubmed.ncbi.nlm.nih.gov/25354011/
379. Boehringer, A, Adam, P, Schnabl, S, Häfner, HM, Breuninger, H, Analysis of incomplete excisions of basal-cell carcinomas after breadloaf microscopy compared with 3D-microscopy: a prospective randomized and blinded study., J Cutan Pathol, 2015. 42 (8)(8): p. 542-53., https://pubmed.ncbi.nlm.nih.gov/25975523/
380. Kofler, L, Breuninger, H, Schreiber, RH, Eichner, M, Häfner, HM, Schnabl, SM, Three-dimensional histology vs. serial section histology in the treatment of primary basal cell carcinoma: a randomized, prospective, blinded study of 569 tumours., J Eur Acad Dermatol Venereol, 2021. 35 (6)(6): p. 1323-1330., https://pubmed.ncbi.nlm.nih.gov/33539573/
381. Friedman, N. R., Prognostic factors for local recurrence, metastases, and survival rates in squamous cell carcinoma of the skin, ear, and lip, J Am Acad Dermatol, 1993. 28(2 Pt 1): p. 281-2., https://www.ncbi.nlm.nih.gov/pubmed/8432936
382. Thomas, D. J., King, A. R., Peat, B. G., Excision margins for nonmelanotic skin cancer, Plast Reconstr Surg, 2003. 112(1): p. 57-63., https://www.ncbi.nlm.nih.gov/pubmed/12832877
383. Breuninger, H., Schaumburg-Lever, G., Control of excisional margins by conventional histopathological techniques in the treatment of skin tumours. An alternative to Mohs' technique, J Pathol, 1988. 154(2): p. 167-71., http://onlinelibrary.wiley.com/doi/10.1002/path.1711540209/abstract
384. Stratigos, AJ, Garbe, C, Dessinioti, C, Lebbe, C, Bataille, V, Bastholt, L, et.al. European interdisciplinary guideline on invasive squamous cell carcinoma of the skin: Part 2. Treatment., Eur J Cancer, 2020. 128 (): p. 83-102., https://pubmed.ncbi.nlm.nih.gov/32113942/
385. Muller, F. M., Dawe, R. S., Moseley, H., Fleming, C. J., Randomized comparison of Mohs micrographic surgery and surgical excision for small nodular basal cell carcinoma: tissue-sparing outcome, Dermatol Surg, 2009. 35(9): p. 1349-54., https://www.ncbi.nlm.nih.gov/pubmed/19500127
386. Brodland, D. G., Zitelli, J. A., Surgical margins for excision of primary cutaneous squamous cell carcinoma, J Am Acad Dermatol, 1992. 27(2 Pt 1): p. 241-8., https://www.ncbi.nlm.nih.gov/pubmed/1430364
387. Bogdanov-Berezovsky, A., Cohen, A. D., Glesinger, R., Cagnano, E., Rosenberg, L., Risk factors for incomplete excision of squamous cell carcinomas, J Dermatolog Treat, 2005. 16(5-6): p. 341-4., https://www.ncbi.nlm.nih.gov/pubmed/16428157
388. Nemet, A. Y., Deckel, Y., Martin, P. A., Kourt, G., Chilov, M., Sharma, V., et.al. Management of periocular basal and squamous cell carcinoma: a series of 485 cases, Am J Ophthalmol, 2006. 142(2): p. 293-7., https://www.ncbi.nlm.nih.gov/pubmed/16876511
389. Phillips, TJ, Harris, BN, Moore, MG, Farwell, DG, Bewley, AF, Pathological margins and advanced cutaneous squamous cell carcinoma of the head and neck., J Otolaryngol Head Neck Surg, 2019. 48 (1)(1): p. 55., https://pubmed.ncbi.nlm.nih.gov/31653276/
390. Bovill, E. S., Banwell, P. E., Re-excision of incompletely excised cutaneous squamous cell carcinoma: histological findings influence prognosis, J Plast Reconstr Aesthet Surg, 2012. 65(10): p. 1390-5., https://www.ncbi.nlm.nih.gov/pubmed/22652292
391. Tan, P. Y., Ek, E., Su, S., Giorlando, F., Dieu, T., Incomplete excision of squamous cell carcinoma of the skin: a prospective observational study, Plast Reconstr Surg, 2007. 120(4): p. 910-6., https://www.ncbi.nlm.nih.gov/pubmed/17805118
392. Hansen, C., Wilkinson, D., Hansen, M., Soyer, H., Factors contributing to incomplete excision of nonmelanoma skin cancer by australian general practitioners, Archives of Dermatology, 2009. 145(11): p. 1253-1260., https://www.ncbi.nlm.nih.gov/pubmed/19917954
393. Mohs, F. E., Guyer, M. F., Pre-excisional Fixation of Tissues in the Treatment of Cancer in Rats, Cancer Research, 1941. 1(1): p. 49-51., http://cancerres.aacrjournals.org/content/canres/1/1/49.full.pdf
394. Drepper, H., Systematic Histological Control of the Tumor Bed as an Advance in the Operative Removal of Deep Facial Skin Cancers, Hautarzt, 1963. 14: p. 420-3., https://www.ncbi.nlm.nih.gov/pubmed/14051771
395. Mohs, F. E., Chemosurgery: microscopically controlled surgery for skin cancer--past, present and future, J Dermatol Surg Oncol, 1978. 4(1): p. 41-54., https://www.ncbi.nlm.nih.gov/pubmed/618934
396. Mohs, F. E., Chemosurgery for the microscopically controlled excision of cutaneous cancer, Head Neck Surg, 1978. 1(2): p. 150-66., https://www.ncbi.nlm.nih.gov/pubmed/755808
397. Burg, G., Hirsch, R. D., Konz, B., Braun-Falco, O., Histographic surgery: accuracy of visual assessment of the margins of basal-cell epithelioma, J Dermatol Surg, 1975. 1(3): p. 21-4., https://www.ncbi.nlm.nih.gov/pubmed/1223161
398. Löser, CR, Rompel, R, Möhrle, M, Häfner, HM, Kunte, C, Hassel, J, et.al. S1 guideline: microscopically controlled surgery (MCS)., J Dtsch Dermatol Ges, 2015. 13 (9)(9): p. 942-51., https://pubmed.ncbi.nlm.nih.gov/26882393/
399. Kauvar, A. N., Arpey, C. J., Hruza, G., Olbricht, S. M., Bennett, R., Mahmoud, B. H., Consensus for Nonmelanoma Skin Cancer Treatment, Part II: Squamous Cell Carcinoma, Including a Cost Analysis of Treatment Methods, Dermatol Surg, 2015. 41(11): p. 1214-40., https://www.ncbi.nlm.nih.gov/pubmed/26445288
400. Breuninger, H, Eigentler, T, Häfner, HM, Leiter, U, None, J Dtsch Dermatol Ges, 2019. 17 (10)(10): p. 999-1004., https://pubmed.ncbi.nlm.nih.gov/31631533/
401. Moehrle, M., Breuninger, H., Röcken, M., A confusing world: what to call histology of three-dimensional tumour margins?, Journal of the European Academy of Dermatology and Venereology, 2007. 21(5): p. 591-595., https://www.ncbi.nlm.nih.gov/pubmed/17447971
402. Waldman, A, Schmults, C, Cutaneous Squamous Cell Carcinoma., Hematol Oncol Clin North Am, 2019. 33 (1)(1): p. 1-12., https://pubmed.ncbi.nlm.nih.gov/30497667/
403. Hafner, H. M., Breuninger, H., Moehrle, M., Trilling, B., Krimmel, M., 3D histology-guided surgery for basal cell carcinoma and squamous cell carcinoma: recurrence rates and clinical outcome, Int J Oral Maxillofac Surg, 2011. 40(9): p. 943-8., https://www.ncbi.nlm.nih.gov/pubmed/21600736
404. Griffiths, R. W., Feeley, K., Suvarna, S. K., Audit of clinical and histological prognostic factors in primary invasive squamous cell carcinoma of the skin: assessment in a minimum 5 year follow-up study after conventional excisional surgery, Br J Plast Surg, 2002. 55(4): p. 287-92., https://www.ncbi.nlm.nih.gov/pubmed/12160533
405. Lansbury, L., Bath-Hextall, F., Perkins, W., Stanton, W., Leonardi-Bee, J., Interventions for non-metastatic squamous cell carcinoma of the skin: systematic review and pooled analysis of observational studies, Bmj, 2013. 347: p. f6153., https://www.ncbi.nlm.nih.gov/pubmed/24191270
406. Jenkins, G., Smith, A. B., Kanatas, A. N., Houghton, D. R., Telfer, M. R., Anatomical restrictions in the surgical excision of scalp squamous cell carcinomas: does this affect local recurrence and regional nodal metastases?, Int J Oral Maxillofac Surg, 2014. 43(2): p. 142-6., https://www.ncbi.nlm.nih.gov/pubmed/24128939
407. Baker, N. J., Webb, A. A., Macpherson, D., Surgical management of cutaneous squamous cell carcinoma of the head and neck, Br J Oral Maxillofac Surg, 2001. 39(2): p. 87-90., https://www.ncbi.nlm.nih.gov/pubmed/11286440
408. Chren, Mary-Margaret, Linos, Eleni, Torres, Jeanette S., Stuart, Sarah E., Parvataneni, Rupa, Boscardin, W. John, Tumor Recurrence 5 Years after Treatment of Cutaneous Basal Cell Carcinoma and Squamous Cell Carcinoma, Journal of Investigative Dermatology, 2013. 133(5): p. 1188-1196., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711403/
409. Sepehripour, S, Dawood, O, Hatter, S, Williams, L, Zahd, Z, Liebmann, R, et.al. An assessment of histological margins and recurrence of completely excised cutaneous SCC., J Plast Reconstr Aesthet Surg, 2020. 73 (5)(5): p. 899-903., https://pubmed.ncbi.nlm.nih.gov/32184053/
410. Thiem, DGE, Scharr, K, Pabst, AM, Saka, B, Kämmerer, PW, Facial cutaneous squamous cell carcinoma - microscopic safety margins and their impact on developing local recurrences., J Craniomaxillofac Surg, 2020. 48 (1)(1): p. 49-55., https://pubmed.ncbi.nlm.nih.gov/31810842/
411. Perkins, W., Who should have Mohs micrographic surgery?, Curr Opin Otolaryngol Head Neck Surg, 2010. 18(4): p. 283-9., https://www.ncbi.nlm.nih.gov/pubmed/20613530
412. Leibovitch, I., Huilgol, S. C., Selva, D., Hill, D., Richards, S., Paver, R., Cutaneous squamous cell carcinoma treated with Mohs micrographic surgery in Australia II. Perineural invasion, J Am Acad Dermatol, 2005. 53(2): p. 261-6., https://www.ncbi.nlm.nih.gov/pubmed/16021121
413. Robins, Perry, Dzubow, Leonard M., Rigel, Darrell S., Squamous-Cell Carcinoma Treated by Mohs' Surgery, The Journal of Dermatologic Surgery and Oncology, 1981. 7(10): p. 800-801., http://dx.doi.org/10.1111/j.1524-4725.1981.tb00168.x
414. Mohs, F. E., Snow, S. N., Microscopically controlled surgical treatment for squamous cell carcinoma of the lower lip, Surg Gynecol Obstet, 1985. 160(1): p. 37-41., https://www.ncbi.nlm.nih.gov/pubmed/3880619
415. Holmkvist, K. A., Roenigk, R. K., Squamous cell carcinoma of the lip treated with Mohs micrographic surgery: outcome at 5 years, J Am Acad Dermatol, 1998. 38(6 Pt 1): p. 960-6., https://www.ncbi.nlm.nih.gov/pubmed/9632005
416. Marrazzo, G, Zitelli, JA, Brodland, D, Clinical outcomes in high-risk squamous cell carcinoma patients treated with Mohs micrographic surgery alone., J Am Acad Dermatol, 2019. 80 (3)(3): p. 633-638., https://pubmed.ncbi.nlm.nih.gov/30244064/
417. Kofler, L, Breuninger, H, Schulz, C, Häfner, HM, Kofler, K, Local Recurrence Rates of Skin Tumors After Resection With Complete Circumferential Peripheral and Deep Margin Assessment-Identification of High-Risk Entities., Dermatol Surg, 2021. 47 (2)(2): p. e31-e36., https://pubmed.ncbi.nlm.nih.gov/33565775/
418. Xiong, DD, Beal, BT, Varra, V, Rodriguez, M, Cundall, H, Woody, NM, et.al. Outcomes in intermediate-risk squamous cell carcinomas treated with Mohs micrographic surgery compared with wide local excision., J Am Acad Dermatol, 2020. 82 (5)(5): p. 1195-1204., https://pubmed.ncbi.nlm.nih.gov/31887322/
419. Loser, C. R., Rompel, R., Mohrle, M., Hafner, H. M., Kunte, C., Hassel, J., et.al. S1 guideline: microscopically controlled surgery (MCS), J Dtsch Dermatol Ges, 2015. 13(9): p. 942-51., https://www.ncbi.nlm.nih.gov/pubmed/20337775
420. Allen, J. E., Stolle, L. B., Utility of sentinel node biopsy in patients with high-risk cutaneous squamous cell carcinoma, Eur J Surg Oncol, 2015. 41(2): p. 197-200., https://www.ncbi.nlm.nih.gov/pubmed/25468745
421. Demir, H., Isken, T., Kus, E., Ziya Tan, Y., Isgoren, S., Daglioz Gorur, G., et.al. Sentinel lymph node biopsy with a gamma probe in patients with high-risk cutaneous squamous cell carcinoma: follow-up results of sentinel lymph node-negative patients, Nucl Med Commun, 2011. 32(12): p. 1216-22., https://www.ncbi.nlm.nih.gov/pubmed/21968433
422. Fukushima, S., Masuguchi, S., Igata, T., Harada, M., Aoi, J., Miyashita, A., et.al. Evaluation of sentinel node biopsy for cutaneous squamous cell carcinoma, J Dermatol, 2014. 41(6): p. 539-41., https://www.ncbi.nlm.nih.gov/pubmed/24909214
423. Ahmed, M. M., Moore, B. A., Schmalbach, C. E., Utility of head and neck cutaneous squamous cell carcinoma sentinel node biopsy: a systematic review, Otolaryngol Head Neck Surg, 2014. 150(2): p. 180-7., https://www.ncbi.nlm.nih.gov/pubmed/24201060
424. Kwon, S., Dong, Z. M., Wu, P. C., Sentinel lymph node biopsy for high-risk cutaneous squamous cell carcinoma: clinical experience and review of literature, World J Surg Oncol, 2011. 9: p. 80., https://www.ncbi.nlm.nih.gov/pubmed/21771334
425. Ross, A. S., Schmults, C. D., Sentinel lymph node biopsy in cutaneous squamous cell carcinoma: a systematic review of the English literature, Dermatol Surg, 2006. 32(11): p. 1309-21., https://www.ncbi.nlm.nih.gov/pubmed/17083582
426. Durham, A. B., Lowe, L., Malloy, K. M., McHugh, J. B., Bradford, C. R., Chubb, H., et.al. Sentinel Lymph Node Biopsy for Cutaneous Squamous Cell Carcinoma on the Head and Neck, JAMA Otolaryngol Head Neck Surg, 2016. 142(12): p. 1171-1176., https://www.ncbi.nlm.nih.gov/pubmed/27438434
427. Dwojak, Sunshine, Emerick, Kevin S., Sentinel lymph node biopsy for cutaneous head and neck malignancies, Expert Review of Anticancer Therapy, 2015. 15(3): p. 305-315., https://doi.org/10.1586/14737140.2015.990441
428. Gore, S. M., Shaw, D., Martin, R. C., Kelder, W., Roth, K., Uren, R., et.al. Prospective study of sentinel node biopsy for high-risk cutaneous squamous cell carcinoma of the head and neck, Head Neck, 2016. 38 Suppl 1: p. E884-9., https://www.ncbi.nlm.nih.gov/pubmed/25965008
429. Krediet, J. T., Beyer, M., Lenz, K., Ulrich, C., Lange-Asschenfeldt, B., Stockfleth, E., et.al. Sentinel lymph node biopsy and risk factors for predicting metastasis in cutaneous squamous cell carcinoma, Br J Dermatol, 2015. 172(4): p. 1029-36., https://www.ncbi.nlm.nih.gov/pubmed/25362868
430. Leiter, U., Gutzmer, R., Alter, M., Ulrich, C., Lonsdorf, A. S., Sachse, M. M., et.al. Kutanes Plattenepithelkarzinom, Der Hautarzt, 2016. 67(11): p. 857-866., https://doi.org/10.1007/s00105-016-3875-2
431. Navarrete-Dechent, Cristian, Veness, Michael J., Droppelmann, Nicolas, Uribe, Pablo, Cutaneous squamous cell carcinoma and the emerging role of sentinel lymph node biopsy: a review, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia, 2018., http://europepmc.org/abstract/MED/29485258, https://doi.org/10.23736/S0392-0488.18.05936-9
432. Navarrete-Dechent, C., Veness, M. J., Droppelmann, N., Uribe, P., High-risk cutaneous squamous cell carcinoma and the emerging role of sentinel lymph node biopsy: A literature review, J Am Acad Dermatol, 2015. 73(1): p. 127-37., https://www.ncbi.nlm.nih.gov/pubmed/26089049
433. Silberstein, E., Sofrin, E., Bogdanov-Berezovsky, A., Nash, M., Segal, N., Lymph Node Metastasis in Cutaneous Head and Neck Squamous Cell Carcinoma, Dermatol Surg, 2015. 41(10): p. 1126-9., https://www.ncbi.nlm.nih.gov/pubmed/26372123
434. Maruyama, H., Tanaka, R., Fujisawa, Y., Nakamura, Y., Ito, S., Fujimoto, M., Availability of sentinel lymph node biopsy for cutaneous squamous cell carcinoma, J Dermatol, 2016., https://www.ncbi.nlm.nih.gov/pubmed/27666747
435. Kofler, L, Kofler, K, Schulz, C, Breuninger, H, Häfner, HM, Sentinel lymph node biopsy for high-thickness cutaneous squamous cell carcinoma., Arch Dermatol Res, 2021. 313 (2)(2): p. 119-126., https://pubmed.ncbi.nlm.nih.gov/32385689/
436. Fu, T., Aasi, S. Z., Hollmig, S. T., Management of High-Risk Squamous Cell Carcinoma of the Skin, Curr Treat Options Oncol, 2016. 17(7): p. 34., https://www.ncbi.nlm.nih.gov/pubmed/27262708
437. Renzi, C., Caggiati, A., Mannooranparampil, T. J., Passarelli, F., Tartaglione, G., Pennasilico, G. M., et.al. Sentinel lymph node biopsy for high risk cutaneous squamous cell carcinoma: case series and review of the literature, Eur J Surg Oncol, 2007. 33(3): p. 364-9., https://www.ncbi.nlm.nih.gov/pubmed/17129703
438. Samsanavicius, D., Kaikaris, V., Norvydas, S. J., Liubauskas, R., Valiukeviciene, S., Makstiene, J., et.al. Sentinel lymph node biopsy for high-risk cutaneous squamous cell carcinoma: Analysis of recurrence-free survival, Medicina (Kaunas), 2016. 52(5): p. 276-282., https://www.ncbi.nlm.nih.gov/pubmed/27746117
439. Schmitt, A. R., Brewer, J. D., Bordeaux, J. S., Baum, C. L., Staging for cutaneous squamous cell carcinoma as a predictor of sentinel lymph node biopsy results: meta-analysis of American Joint Committee on Cancer criteria and a proposed alternative system, JAMA Dermatol, 2014. 150(1): p. 19-24., https://www.ncbi.nlm.nih.gov/pubmed/24226651
440. Takahashi, A., Imafuku, S., Nakayama, J., Nakaura, J., Ito, K., Shibayama, Y., Sentinel node biopsy for high-risk cutaneous squamous cell carcinoma, Eur J Surg Oncol, 2014. 40(10): p. 1256-62., https://www.ncbi.nlm.nih.gov/pubmed/24953417
441. Ebrahimi, A., Moncrieff, M. D., Clark, J. R., Shannon, K. F., Gao, K., Milross, C. G., et.al. Predicting the pattern of regional metastases from cutaneous squamous cell carcinoma of the head and neck based on location of the primary, Head Neck, 2010. 32(10): p. 1288-94., https://www.ncbi.nlm.nih.gov/pubmed/20091686
442. Gurney, B., Newlands, C., Management of regional metastatic disease in head and neck cutaneous malignancy. 1. Cutaneous squamous cell carcinoma, Br J Oral Maxillofac Surg, 2014. 52(4): p. 294-300., https://www.ncbi.nlm.nih.gov/pubmed/24559975
443. Martinez, J. C., Cook, J. L., High-risk cutaneous squamous cell carcinoma without palpable lymphadenopathy: is there a therapeutic role for elective neck dissection?, Dermatol Surg, 2007. 33(4): p. 410-20., https://www.ncbi.nlm.nih.gov/pubmed/17430374
444. Wong, W. K., Morton, R. P., Elective management of cervical and parotid lymph nodes in stage N0 cutaneous squamous cell carcinoma of the head and neck: a decision analysis, Eur Arch Otorhinolaryngol, 2014. 271(11): p. 3011-9., https://www.ncbi.nlm.nih.gov/pubmed/24337900
445. Newlands, C., Currie, R., Memon, A., Whitaker, S., Woolford, T., Non-melanoma skin cancer: United Kingdom National Multidisciplinary Guidelines, The Journal of Laryngology and Otology, 2016. 130(Suppl 2): p. S125-S132., http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873942/
446. Cannon, R. B., Dundar, Y., Thomas, A., Monroe, M. M., Buchmann, L. O., Witt, B. L., et.al. Elective Neck Dissection for Head and Neck Cutaneous Squamous Cell Carcinoma with Skull Base Invasion, Otolaryngol Head Neck Surg, 2017. 156(4): p. 671-676., https://www.ncbi.nlm.nih.gov/pubmed/28366108
447. Herman, M. P., Amdur, R. J., Werning, J. W., Dziegielewski, P. T., Morris, C. G., Mendenhall, W. M., Elective Neck Management for Squamous Cell Carcinoma Metastatic to the Parotid-area Lymph Nodes, International Journal of Radiation Oncology • Biology • Physics 94(4): p. 932., http://dx.doi.org/10.1016/j.ijrobp.2015.12.247
448. Ebrahimi, A., Clark, J. R., Ahmadi, N., Palme, C. E., Morgan, G. J., Veness, M. J., Prognostic significance of disease-free interval in head and neck cutaneous squamous cell carcinoma with nodal metastases, Head Neck, 2013. 35(8): p. 1138-43., https://www.ncbi.nlm.nih.gov/pubmed/23152126
449. Kirke, D. N., Porceddu, S., Wallwork, B. D., Panizza, B., Coman, W. B., Pathologic occult neck disease in patients with metastatic cutaneous squamous cell carcinoma to the parotid, Otolaryngol Head Neck Surg, 2011. 144(4): p. 549-51., https://www.ncbi.nlm.nih.gov/pubmed/21493233
450. Bumpous, J., Metastatic cutaneous squamous cell carcinoma to the parotid and cervical lymph nodes: treatment and outcomes, Curr Opin Otolaryngol Head Neck Surg, 2009. 17(2): p. 122-5., https://www.ncbi.nlm.nih.gov/pubmed/19346945
451. D'Souza, J., Clark, J., Management of the neck in metastatic cutaneous squamous cell carcinoma of the head and neck, Curr Opin Otolaryngol Head Neck Surg, 2011. 19(2): p. 99-105., https://www.ncbi.nlm.nih.gov/pubmed/21297477
452. Kosec, A., Svetina, L., Luksic, I., Significance of clinical stage, extent of surgery and outcome in cutaneous squamous cell carcinoma of the head and neck, Int J Oral Maxillofac Surg, 2013. 42(1): p. 82-8., https://www.ncbi.nlm.nih.gov/pubmed/23137734
453. Schmidt, C., Martin, J. M., Khoo, E., Plank, A., Grigg, R., Outcomes of nodal metastatic cutaneous squamous cell carcinoma of the head and neck treated in a regional center, Head Neck, 2015. 37(12): p. 1808-15., https://www.ncbi.nlm.nih.gov/pubmed/24995842
454. Veness, M. J., Palme, C. E., Smith, M., Cakir, B., Morgan, G. J., Kalnins, I., Cutaneous head and neck squamous cell carcinoma metastatic to cervical lymph nodes (nonparotid): a better outcome with surgery and adjuvant radiotherapy, Laryngoscope, 2003. 113(10): p. 1827-33., https://www.ncbi.nlm.nih.gov/pubmed/14520114
455. Gooris, P. J., Vermey, A., de Visscher, J. G., Burlage, F. R., Roodenburg, J. L., Supraomohyoid neck dissection in the management of cervical lymph node metastases of squamous cell carcinoma of the lower lip, Head Neck, 2002. 24(7): p. 678-83., https://www.ncbi.nlm.nih.gov/pubmed/12112542
456. Kuscu, O., Bajin, M. D., Suslu, N., Hosal, A. S., The role of suprahyoid neck dissection in the treatment of squamous cell carcinoma of the lower lip: 20 years' experience at a Tertiary Center, J Craniomaxillofac Surg, 2016. 44(9): p. 1404-7., https://www.ncbi.nlm.nih.gov/pubmed/27427340
457. Robbins, K. T., Clayman, G., Levine, P. A., Medina, J., Sessions, R., Shaha, A., et.al. Neck dissection classification update: revisions proposed by the American Head and Neck Society and the American Academy of Otolaryngology-Head and Neck Surgery, Arch Otolaryngol Head Neck Surg, 2002. 128(7): p. 751-8., https://www.ncbi.nlm.nih.gov/pubmed/12117328
458. Vartanian, J. G., Carvalho, A. L., de Araujo Filho, M. J., Junior, M. H., Magrin, J., Kowalski, L. P., Predictive factors and distribution of lymph node metastasis in lip cancer patients and their implications on the treatment of the neck, Oral Oncol, 2004. 40(2): p. 223-7., https://www.ncbi.nlm.nih.gov/pubmed/14693248
459. Clark, R. R., Soutar, D. S., Lymph node metastases from auricular squamous cell carcinoma. A systematic review and meta-analysis, J Plast Reconstr Aesthet Surg, 2008. 61(10): p. 1140-7., https://www.ncbi.nlm.nih.gov/pubmed/18675609
460. Peiffer, N., Kutz, J. W., Jr., Myers, L. L., Isaacson, B., Sumer, B. D., Truelson, J. M., et.al. Patterns of regional metastasis in advanced stage cutaneous squamous cell carcinoma of the auricle, Otolaryngol Head Neck Surg, 2011. 144(1): p. 36-42., https://www.ncbi.nlm.nih.gov/pubmed/21493384
461. Turner, S. J., Morgan, G. J., Palme, C. E., Veness, M. J., Metastatic cutaneous squamous cell carcinoma of the external ear: a high-risk cutaneous subsite, J Laryngol Otol, 2010. 124(1): p. 26-31., https://www.ncbi.nlm.nih.gov/pubmed/19775493
462. Werner JA, Patterns of metastasis in head and neck cancer, Cancer Treat Res 135:203–207, 2007., https://pubmed.ncbi.nlm.nih.gov/17953418/
463. Uren, R. F., Lymphatic drainage of the skin, Ann Surg Oncol, 2004. 11(3 Suppl): p. 179s-85s., https://www.ncbi.nlm.nih.gov/pubmed/15023748
464. Vauterin, T. J., Veness, M. J., Morgan, G. J., Poulsen, M. G., O'Brien, C. J., Patterns of lymph node spread of cutaneous squamous cell carcinoma of the head and neck, Head Neck, 2006. 28(9): p. 785-91., https://www.ncbi.nlm.nih.gov/pubmed/16783833
465. Hoetzenecker, W, Guenova, E, Böttinger, TU, Häfner, HM, Breuninger, H, Mapping of specific sentinel node locations for skin cancer of the head., Eur J Dermatol 21 (3)(3): p. 354-8., https://pubmed.ncbi.nlm.nih.gov/21680279/
466. Shao, Angus, Wong, Danny K. C., McIvor, Nicholas P., Mylnarek, Alex M., Chaplin, John M., Izzard, Mark E., et.al. Parotid metastatic disease from cutaneous squamous cell carcinoma: Prognostic role of facial nerve sacrifice, lateral temporal bone resection, immune status and P‐stage, Head & Neck, 2014. 36(4): p. 545-550., https://onlinelibrary.wiley.com/doi/abs/10.1002/hed.23323
467. Sweeny, L., Zimmerman, T., Carroll, W. R., Schmalbach, C. E., Day, K. E., Rosenthal, E. L., Head and neck cutaneous squamous cell carcinoma requiring parotidectomy: prognostic indicators and treatment selection, Otolaryngol Head Neck Surg, 2014. 150(4): p. 610-7., https://www.ncbi.nlm.nih.gov/pubmed/24474713
468. Dunne, A. A., Budach, V. G., Wagner, W., Werner, J. A., Management of N0 neck in head and neck cancer: current controversies, Onkologie, 2004. 27(4): p. 363-7., https://www.ncbi.nlm.nih.gov/pubmed/15347891
469. Ferlito, A., Rinaldo, A., Silver, C. E., Gourin, C. G., Shah, J. P., Clayman, G. L., et.al. Elective and therapeutic selective neck dissection, Oral Oncol, 2006. 42(1): p. 14-25., https://www.ncbi.nlm.nih.gov/pubmed/15979381
470. Ferlito, A., Rinaldo, A., Silver, C. E., Shah, J. P., Suarez, C., Medina, J. E., et.al. Neck dissection: then and now, Auris Nasus Larynx, 2006. 33(4): p. 365-74., https://www.ncbi.nlm.nih.gov/pubmed/16889923
471. Nissen, C. V., Heerfordt, I. M., Wiegell, S. R., Mikkelsen, C. S., Wulf, H. C., Pretreatment with 5-Fluorouracil Cream Enhances the Efficacy of Daylight-mediated Photodynamic Therapy for Actinic Keratosis, Acta Derm Venereol, 2017. 97(5): p. 617-621., https://www.ncbi.nlm.nih.gov/pubmed/28093604
472. Werner, J. A., Dunne, A. A., Lippert, B. M., [Indications for neck operation in undiagnosed lymph node metastases. 2. Neck dissection in the clinical N0 neck], Hno, 2002. 50(4): p. 370-8; quiz 378-9., https://www.ncbi.nlm.nih.gov/pubmed/12063698
473. Mendenhall, W. M., Amdur, R. J., Hinerman, R. W., Cognetta, A. B., Mendenhall, N. P., Radiotherapy for cutaneous squamous and basal cell carcinomas of the head and neck, Laryngoscope, 2009. 119(10): p. 1994-9., https://www.ncbi.nlm.nih.gov/pubmed/19688856
474. Adelstein DJ, Lavertu P, Saxton JP, Secic M, Wood BG, Wanamaker JR, et.al. Mature results of a phase III randomized trial comparing concurrent chemoradiotherapy with radiation therapy alone in patients with stage III and IV squamous cell carcinoma of the head and neck, Cancer, 2000. 88(4): p. 876-83., https://www.ncbi.nlm.nih.gov/pubmed/10679658
475. Cooper, J. S., Zhang, Q., Pajak, T. F., Forastiere, A. A., Jacobs, J., Saxman, S. B., et.al. Long-term follow-up of the RTOG 9501/intergroup phase III trial: postoperative concurrent radiation therapy and chemotherapy in high-risk squamous cell carcinoma of the head and neck, Int J Radiat Oncol Biol Phys, 2012. 84(5): p. 1198-205., https://www.ncbi.nlm.nih.gov/pubmed/22749632
476. Nottage, M. K., Lin, C., Hughes, B. G., Kenny, L., Smith, D. D., Houston, K., et.al. Prospective study of definitive chemoradiation in locally or regionally advanced squamous cell carcinoma of the skin, Head Neck, 2017. 39(4): p. 679-683., https://www.ncbi.nlm.nih.gov/pubmed/28032670
477. Lu, SM, Lien, WW, Concurrent Radiotherapy With Cetuximab or Platinum-based Chemotherapy for Locally Advanced Cutaneous Squamous Cell Carcinoma of the Head and Neck., Am J Clin Oncol, 2018. 41 (1)(1): p. 95-99., https://pubmed.ncbi.nlm.nih.gov/26353121/
478. Mendenhall, W. M., Amdur, R. J., Hinerman, R. W., Werning, J. W., Malyapa, R. S., Villaret, D. B., et.al. Skin cancer of the head and neck with perineural invasion, Am J Clin Oncol, 2007. 30(1): p. 93-6., https://www.ncbi.nlm.nih.gov/pubmed/17278901
479. Tanvetyanon, T., Padhya, T., McCaffrey, J., Kish, J. A., Deconti, R. C., Trotti, A., et.al. Postoperative concurrent chemotherapy and radiotherapy for high-risk cutaneous squamous cell carcinoma of the head and neck, Head Neck, 2015. 37(6): p. 840-5., https://www.ncbi.nlm.nih.gov/pubmed/24623654
480. Veness, M. J., Treatment recommendations in patients diagnosed with high-risk cutaneous squamous cell carcinoma, Australas Radiol, 2005. 49(5): p. 365-76., https://www.ncbi.nlm.nih.gov/pubmed/16174174
481. Han, A., Ratner, D., What is the role of adjuvant radiotherapy in the treatment of cutaneous squamous cell carcinoma with perineural invasion?, Cancer, 2007. 109(6): p. 1053-9., https://www.ncbi.nlm.nih.gov/pubmed/17279578
482. Wang, J. T., Palme, C. E., Morgan, G. J., Gebski, V., Wang, A. Y., Veness, M. J., Predictors of outcome in patients with metastatic cutaneous head and neck squamous cell carcinoma involving cervical lymph nodes: Improved survival with the addition of adjuvant radiotherapy, Head Neck, 2012. 34(11): p. 1524-8., https://www.ncbi.nlm.nih.gov/pubmed/22109745
483. Veness, M. J., Morgan, G. J., Palme, C. E., Gebski, V., Surgery and adjuvant radiotherapy in patients with cutaneous head and neck squamous cell carcinoma metastatic to lymph nodes: combined treatment should be considered best practice, Laryngoscope, 2005. 115(5): p. 870-5., https://www.ncbi.nlm.nih.gov/pubmed/15867656
484. Sahovaler, A, Krishnan, RJ, Yeh, DH, Zhou, Q, Palma, D, Fung, K, et.al. Outcomes of Cutaneous Squamous Cell Carcinoma in the Head and Neck Region With Regional Lymph Node Metastasis: A Systematic Review and Meta-analysis., JAMA Otolaryngol Head Neck Surg, 2019. 145 (4)(4): p. 352-360., https://pubmed.ncbi.nlm.nih.gov/30844021/
485. Zhang, J, Wang, Y, Wijaya, WA, Liang, Z, Chen, J, Efficacy and prognostic factors of adjuvant radiotherapy for cutaneous squamous cell carcinoma: A systematic review and meta-analysis., J Eur Acad Dermatol Venereol, 2021. 35 (9)(9): p. 1777-1787., https://pubmed.ncbi.nlm.nih.gov/33930213/
486. Porceddu, SV, Bressel, M, Poulsen, MG, Stoneley, A, Veness, MJ, Kenny, LM, et.al. Postoperative Concurrent Chemoradiotherapy Versus Postoperative Radiotherapy in High-Risk Cutaneous Squamous Cell Carcinoma of the Head and Neck: The Randomized Phase III TROG 05.01 Trial., J Clin Oncol, 2018. 36 (13)(13): p. 1275-1283., https://pubmed.ncbi.nlm.nih.gov/29537906/
487. Trosman, SJ, Zhu, A, Nicolli, EA, Leibowitz, JM, Sargi, ZB, High-Risk Cutaneous Squamous Cell Cancer of the Head and Neck: Risk Factors for Recurrence and Impact of Adjuvant Treatment., Laryngoscope, 2021. 131 (1)(1): p. E136-E143., https://pubmed.ncbi.nlm.nih.gov/32065413/
488. Palmer, JD, Schneider, CJ, Hockstein, N, Hanlon, AL, Silberg, J, Strasser, J, et.al. Combination of post-operative radiotherapy and cetuximab for high-risk cutaneous squamous cell cancer of the head and neck: A propensity score analysis., Oral Oncol, 2018. 78 (): p. 102-107., https://pubmed.ncbi.nlm.nih.gov/29496036/
489. Sapijaszko, M., Zloty, D., Bourcier, M., Poulin, Y., Janiszewski, P., Ashkenas, J., Non-melanoma Skin Cancer in Canada Chapter 5: Management of Squamous Cell Carcinoma, J Cutan Med Surg, 2015. 19(3): p. 249-59., https://www.ncbi.nlm.nih.gov/pubmed/25922470
490. Waxweiler, W., Sigmon, J. R., Sheehan, D. J., Adjunctive radiotherapy in the treatment of cutaneous squamous cell carcinoma with perineural invasion, J Surg Oncol, 2011. 104(1): p. 104-5., https://www.ncbi.nlm.nih.gov/pubmed/21360531
491. Amoils, M., Lee, C. S., Sunwoo, J., Aasi, S. Z., Hara, W., Kim, J., et.al. Node-positive cutaneous squamous cell carcinoma of the head and neck: Survival, high-risk features, and adjuvant chemoradiotherapy outcomes, Head Neck, 2017. 39(5): p. 881-885., https://www.ncbi.nlm.nih.gov/pubmed/28252823
492. Chen, A. M., Grekin, R. C., Garcia, J., Bucci, M. K., Margolis, L. W., Radiation therapy for cutaneous squamous cell carcinoma involving the parotid area lymph nodes: dose and volume considerations, Int J Radiat Oncol Biol Phys, 2007. 69(5): p. 1377-80., https://www.ncbi.nlm.nih.gov/pubmed/17689882
493. Jol, J. A., van Velthuysen, M. L., Hilgers, F. J., Keus, R. B., Neering, H., Balm, A. J., Treatment results of regional metastasis from cutaneous head and neck squamous cell carcinoma, Eur J Surg Oncol, 2003. 29(1): p. 81-6., https://www.ncbi.nlm.nih.gov/pubmed/12559082
494. Chua, M. S., Veness, M. J., Morgan, G., Shakespeare, T., Hehir, A., Gebski, V., et.al. Parotid lymph-node metastases from cutaneous squamous-cell carcinomas: treatment outcome and prognostic factors following surgery and adjuvant radiotherapy, Australas Radiol, 2002. 46(2): p. 174-9., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422189/
495. Hong, T. S., Kriesel, K. J., Hartig, G. K., Harari, P. M., Parotid area lymph node metastases from cutaneous squamous cell carcinoma: implications for diagnosis, treatment, and prognosis, Head Neck, 2005. 27(10): p. 851-6., https://www.ncbi.nlm.nih.gov/pubmed/16114004
496. Strassen, U., Hofauer, B., Jacobi, C., Knopf, A., Management of locoregional recurrence in cutaneous squamous cell carcinoma of the head and neck, Eur Arch Otorhinolaryngol, 2017. 274(1): p. 501-506., https://www.ncbi.nlm.nih.gov/pubmed/27498202
497. Bertino, G., Sersa, G., De Terlizzi, F., Occhini, A., Plaschke, C. C., Groselj, A., et.al. European Research on Electrochemotherapy in Head and Neck Cancer (EURECA) project: Results of the treatment of skin cancer, Eur J Cancer, 2016. 63: p. 41-52., https://www.ncbi.nlm.nih.gov/pubmed/27267144
498. Campana, L. G., Testori, A., Curatolo, P., Quaglino, P., Mocellin, S., Framarini, M., et.al. Treatment efficacy with electrochemotherapy: A multi-institutional prospective observational study on 376 patients with superficial tumors, Eur J Surg Oncol, 2016. 42(12): p. 1914-1923., https://www.ncbi.nlm.nih.gov/pubmed/27424789
499. Kreuter, Alexander, Eijk, Tina, Lehmann, Percy, Fischer, Matthias, Horn, Thomas, Assaf, Chalid, et.al. Electrochemotherapy in advanced skin tumors and cutaneous metastases – a retrospective multicenter analysis, J Dtsch Dermatol Ges, 2015. 13(4): p. 308-315., https://pubmed.ncbi.nlm.nih.gov/25819239/
500. Pickering, CR, Zhou, JH, Lee, JJ, Drummond, JA, Peng, SA, Saade, RE, et.al. Mutational landscape of aggressive cutaneous squamous cell carcinoma., Clin Cancer Res, 2014. 20 (24)(24): p. 6582-92., https://pubmed.ncbi.nlm.nih.gov/25303977/
501. Amaral, T, Osewold, M, Presser, D, Meiwes, A, Garbe, C, Leiter, U, Advanced cutaneous squamous cell carcinoma: real world data of patient profiles and treatment patterns, J Eur Acad Dermatol Venereol, 2019. 33 Suppl 8 (): p. 44-51., https://pubmed.ncbi.nlm.nih.gov/31658392/
502. Salzmann, M, Leiter, U, Loquai, C, Zimmer, L, Ugurel, S, Gutzmer, R, et.al. Programmed cell death protein 1 inhibitors in advanced cutaneous squamous cell carcinoma: real-world data of a retrospective, multicenter study., Eur J Cancer, 2020. 138 (): p. 125-132., https://pubmed.ncbi.nlm.nih.gov/32882466/
503. Migden, M. R., Rischin, D., Schmults, C. D., Guminski, A., Hauschild, A., Lewis, K. D., et.al. PD-1 Blockade with Cemiplimab in Advanced Cutaneous Squamous-Cell Carcinoma, N Engl J Med, 2018., https://www.ncbi.nlm.nih.gov/pubmed/29863979
504. Rischin, D, Migden, MR, Lim, AM, Schmults, CD, Khushalani, NI, Hughes, BGM, et.al. Phase 2 study of cemiplimab in patients with metastatic cutaneous squamous cell carcinoma: primary analysis of fixed-dosing, long-term outcome of weight-based dosing., J Immunother Cancer, 2020. 8 (1)(1):, https://pubmed.ncbi.nlm.nih.gov/32554615/
505. Migden, MR, Khushalani, NI, Chang, ALS, Lewis, KD, Schmults, CD, Hernandez-Aya, L, et.al. Cemiplimab in locally advanced cutaneous squamous cell carcinoma: results from an open-label, phase 2, single-arm trial., Lancet Oncol, 2020. 21 (2)(2): p. 294-305., https://pubmed.ncbi.nlm.nih.gov/31952975/
506. Maubec, E, Boubaya, M, Petrow, P, Beylot-Barry, M, Basset-Seguin, N, Deschamps, L, et.al. Phase II Study of Pembrolizumab As First-Line, Single-Drug Therapy for Patients With Unresectable Cutaneous Squamous Cell Carcinomas., J Clin Oncol, 2020. 38 (26)(26): p. 3051-3061., https://pubmed.ncbi.nlm.nih.gov/32730186/
507. Grob, JJ, Gonzalez, R, Basset-Seguin, N, Vornicova, O, Schachter, J, Joshi, A, et.al. Pembrolizumab Monotherapy for Recurrent or Metastatic Cutaneous Squamous Cell Carcinoma: A Single-Arm Phase II Trial (KEYNOTE-629)., J Clin Oncol, 2020. 38 (25)(25): p. 2916-2925., https://pubmed.ncbi.nlm.nih.gov/32673170/
508. Behshad, R., Garcia-Zuazaga, J., Bordeaux, J. S., Systemic treatment of locally advanced nonmetastatic cutaneous squamous cell carcinoma: a review of the literature, Br J Dermatol, 2011. 165(6): p. 1169-77., http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.2011.10524.x/abstract
509. Hillen, U, Leiter, U, Haase, S, Kaufmann, R, Becker, J, Gutzmer, R, et.al. Advanced cutaneous squamous cell carcinoma: A retrospective analysis of patient profiles and treatment patterns-Results of a non-interventional study of the DeCOG., Eur J Cancer, 2018. 96 (): p. 34-43., https://pubmed.ncbi.nlm.nih.gov/29665511/
510. Guthrie, T. H., Jr., Porubsky, E. S., Luxenberg, M. N., Shah, K. J., Wurtz, K. L., Watson, P. R., Cisplatin-based chemotherapy in advanced basal and squamous cell carcinomas of the skin: results in 28 patients including 13 patients receiving multimodality therapy, J Clin Oncol, 1990. 8(2): p. 342-6., https://www.ncbi.nlm.nih.gov/pubmed/2405109
511. Sadek, H., Azli, N., Wendling, J. L., Cvitkovic, E., Rahal, M., Mamelle, G., et.al. Treatment of advanced squamous cell carcinoma of the skin with cisplatin, 5-fluorouracil, and bleomycin, Cancer, 1990. 66(8): p. 1692-6., https://www.ncbi.nlm.nih.gov/pubmed/1698529
512. Khansur, T., Kennedy, A., Cisplatin and 5-fluorouracil for advanced locoregional and metastatic squamous cell carcinoma of the skin, Cancer, 1991. 67(8): p. 2030-2., https://www.ncbi.nlm.nih.gov/pubmed/2004320
513. Cartei, G., Cartei, F., Interlandi, G., Meneghini, G., Jop, A., Zingone, G., et.al. Oral 5-fluorouracil in squamous cell carcinoma of the skin in the aged, Am J Clin Oncol, 2000. 23(2): p. 181-4., https://www.ncbi.nlm.nih.gov/pubmed/10776981
514. Lippman, S. M., Parkinson, D. R., Itri, L. M., Weber, R. S., Schantz, S. P., Ota, D. M., et.al. 13-cis-retinoic acid and interferon alpha-2a: effective combination therapy for advanced squamous cell carcinoma of the skin, J Natl Cancer Inst, 1992. 84(4): p. 235-41., https://www.ncbi.nlm.nih.gov/pubmed/1734084
515. Shin, D. M., Khuri, F. R., Glisson, B. S., Ginsberg, L., Papadimitrakopoulou, V. M., Clayman, G., et.al. Phase II study of paclitaxel, ifosfamide, and carboplatin in patients with recurrent or metastatic head and neck squamous cell carcinoma, Cancer, 2001. 91(7): p. 1316-23., https://www.ncbi.nlm.nih.gov/pubmed/11283932
516. Huis In 't Veld, EA, Grünhagen, DJ, Deroose, JP, Nijsten, TEC, Wouters, MWJM, Verhoef, C, et.al. Isolated limb perfusion for unresectable extremity cutaneous squamous cell carcinoma; an effective limb saving strategy., Br J Cancer, 2018. 119 (4)(4): p. 429-434., https://pubmed.ncbi.nlm.nih.gov/29961756/
517. Joseph, K, Alkaabi, K, Warkentin, H, Ghosh, S, Jha, N, Smylie, M, et.al. Cetuximab-radiotherapy combination in the management of locally advanced cutaneous squamous cell carcinoma., J Med Imaging Radiat Oncol, 2019. 63 (2)(2): p. 257-263., https://pubmed.ncbi.nlm.nih.gov/30549229/
518. Maubec, E., Petrow, P., Scheer-Senyarich, I., Duvillard, P., Lacroix, L., Gelly, J., et.al. Phase II study of cetuximab as first-line single-drug therapy in patients with unresectable squamous cell carcinoma of the skin, J Clin Oncol, 2011. 29(25): p. 3419-26., https://www.ncbi.nlm.nih.gov/pubmed/21810686
519. Foote, M. C., McGrath, M., Guminski, A., Hughes, B. G., Meakin, J., Thomson, D., et.al. Phase II study of single-agent panitumumab in patients with incurable cutaneous squamous cell carcinoma, Ann Oncol, 2014. 25(10): p. 2047-52., https://www.ncbi.nlm.nih.gov/pubmed/25091317
520. Lewis, C. M., Glisson, B. S., Feng, L., Wan, F., Tang, X., Wistuba, II, et.al. A phase II study of gefitinib for aggressive cutaneous squamous cell carcinoma of the head and neck, Clin Cancer Res, 2012. 18(5): p. 1435-46., http://clincancerres.aacrjournals.org/content/clincanres/18/5/1435.full.pdf
521. Heath, C. H., Deep, N. L., Nabell, L., Carroll, W. R., Desmond, R., Clemons, L., et.al. Phase I Study of Erlotinib Plus Radiation Therapy in Patients with Advanced Cutaneous Squamous Cell Carcinoma, Int J Radiat Oncol Biol Phys, 2013. 85(5): p. 1275-81., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607201/pdf/nihms428673.pdf
522. Jenni, D., Karpova, M., Mühleisen, B., Mangana, J., Dreier, J., Hafner, J., et.al. A prospective clinical trial to assess lapatinib effects on cutaneous squamous cell carcinoma and actinic keratosis, ESMO Open, 2016. 1(1):, https://pubmed.ncbi.nlm.nih.gov/27843579/
523. Cavalieri, S, Perrone, F, Miceli, R, Ascierto, PA, Locati, LD, Bergamini, C, et.al. Efficacy and safety of single-agent pan-human epidermal growth factor receptor (HER) inhibitor dacomitinib in locally advanced unresectable or metastatic skin squamous cell cancer., Eur J Cancer, 2018. 97 (): p. 7-15., https://pubmed.ncbi.nlm.nih.gov/29734047/
524. Gold, KA, Kies, MS, William, WN, Johnson, FM, Lee, JJ, Glisson, BS, Erlotinib in the treatment of recurrent or metastatic cutaneous squamous cell carcinoma: A single-arm phase 2 clinical trial., Cancer, 2018. 124 (10)(10): p. 2169-2173., https://pubmed.ncbi.nlm.nih.gov/29579331/
525. Leiter, U, Loquai, C, Reinhardt, L, Rafei-Shamsabadi, D, Gutzmer, R, Kaehler, K, et.al. Immune checkpoint inhibition therapy for advanced skin cancer in patients with concomitant hematological malignancy: a retrospective multicenter DeCOG study of 84 patients., J Immunother Cancer, 2020. 8 (2)(2):, https://pubmed.ncbi.nlm.nih.gov/33093156/
526. Salgo, R., Gossmann, J., Schofer, H., Kachel, H. G., Kuck, J., Geiger, H., et.al. Switch to a sirolimus-based immunosuppression in long-term renal transplant recipients: reduced rate of (pre-)malignancies and nonmelanoma skin cancer in a prospective, randomized, assessor-blinded, controlled clinical trial, Am J Transplant, 2010. 10(6): p. 1385-93., https://www.ncbi.nlm.nih.gov/pubmed/20121752
527. Campbell, S. B., Walker, R., Tai, S. S., Jiang, Q., Russ, G. R., Randomized controlled trial of sirolimus for renal transplant recipients at high risk for nonmelanoma skin cancer, Am J Transplant, 2012. 12(5): p. 1146-56., https://www.ncbi.nlm.nih.gov/pubmed/22420843
528. Euvrard , Sylvie, Morelon , Emmanuel, Rostaing , Lionel, Goffin , Eric, Brocard , Anabelle, Tromme , Isabelle, et.al. Sirolimus and Secondary Skin-Cancer Prevention in Kidney Transplantation, New England Journal of Medicine, 2012. 367(4): p. 329-339., http://www.nejm.org/doi/full/10.1056/NEJMoa1204166, http://www.nejm.org/doi/pdf/10.1056/NEJMoa1204166
529. Hoogendijk-van den Akker, J. M., Harden, P. N., Hoitsma, A. J., Proby, C. M., Wolterbeek, R., Bouwes Bavinck, J. N., et.al. Two-year randomized controlled prospective trial converting treatment of stable renal transplant recipients with cutaneous invasive squamous cell carcinomas to sirolimus, J Clin Oncol, 2013. 31(10): p. 1317-23., https://www.ncbi.nlm.nih.gov/pubmed/23358973
530. Tio, M, Rai, R, Ezeoke, OM, McQuade, JL, Zimmer, L, Khoo, C, et.al. Anti-PD-1/PD-L1 immunotherapy in patients with solid organ transplant, HIV or hepatitis B/C infection., Eur J Cancer, 2018. 104 (): p. 137-144., https://pubmed.ncbi.nlm.nih.gov/30347289/
531. Lehmann, K, Eshmuminov, D, Bauerfeind, P, Gubler, C, Veit-Haibach, P, Weber, A, et.al. None, Eur J Surg Oncol, 2017. 43 (1)(1): p. 196-202., https://pubmed.ncbi.nlm.nih.gov/27692533/
532. Hitt, R., Irigoyen, A., Cortes-Funes, H., Grau, J. J., Garcia-Saenz, J. A., Cruz-Hernandez, J. J., Phase II study of the combination of cetuximab and weekly paclitaxel in the first-line treatment of patients with recurrent and/or metastatic squamous cell carcinoma of head and neck, Ann Oncol, 2012. 23(4): p. 1016-22., https://www.ncbi.nlm.nih.gov/pubmed/21865152
533. Vermorken , Jan B., Mesia , Ricard, Rivera , Fernando, Remenar , Eva, Kawecki , Andrzej, Rottey , Sylvie, et.al. Platinum-Based Chemotherapy plus Cetuximab in Head and Neck Cancer, New England Journal of Medicine, 2008. 359(11): p. 1116-1127., http://www.nejm.org/doi/full/10.1056/NEJMoa0802656
534. Vardhan, M, Flaminio, Z, Sapru, S, Tilley, CP, Fu, MR, Comfort, C, et.al. The Microbiome, Malignant Fungating Wounds, and Palliative Care., Front Cell Infect Microbiol, 2019. 9 (): p. 373., https://pubmed.ncbi.nlm.nih.gov/31737576/
535. Kähler, KC, Egberts, F, Gutzmer, R, Palliative treatment of skin metastases in dermato-oncology., J Dtsch Dermatol Ges, 2013. 11 (11)(11): p. 1041-5; quiz 1046., https://pubmed.ncbi.nlm.nih.gov/24015966/
536. Probst, U, Fuhrmann, I, Beyer, L, Wiggermann, P, Electrochemotherapy as a New Modality in Interventional Oncology: A Review., Technol Cancer Res Treat, 2018. 17 (): p. 1533033818785329., https://pubmed.ncbi.nlm.nih.gov/29986632/
537. Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF): Palliativmedizin für Patienten mit einer nicht-heilbaren Krebserkrankung, Langversion 2.2, 2020., https://www.leitlinienprogramm-onkologie.de/leitlinien/palliativmedizin/
538. Teunissen, SC, Wesker, W, Kruitwagen, C, de Haes, HC, Voest, EE, de Graeff, A, Symptom prevalence in patients with incurable cancer: a systematic review., J Pain Symptom Manage, 2007. 34 (1)(1): p. 94-104., https://pubmed.ncbi.nlm.nih.gov/17509812/
539. McCarthy, W. H., Shaw, H. M., Thompson, J. F., Milton, G. W., Time and frequency of recurrence of cutaneous stage I malignant melanoma with guidelines for follow-up study, Surgery, gynecology & obstetrics, 1988. 166(6): p. 497-502., http://europepmc.org/abstract/MED/3375961
540. Wassberg, C., Thorn, M., Yuen, J., Ringborg, U., Hakulinen, T., Second primary cancers in patients with squamous cell carcinoma of the skin: a population-based study in Sweden, Int J Cancer, 1999. 80(4): p. 511-5., https://www.ncbi.nlm.nih.gov/pubmed/9935149
541. Balch, C. M., Gershenwald, J. E., Soong, S. J., Thompson, J. F., Atkins, M. B., Byrd, D. R., et.al. Final version of 2009 AJCC melanoma staging and classification, J Clin Oncol, 2009. 27(36): p. 6199-206., https://www.ncbi.nlm.nih.gov/pubmed/19917835
542. Dancey, A., Rayatt, S., Courthold, J., Roberts, J., Views of UK melanoma patients on routine follow-up care, Br J Plast Surg, 2005. 58(2): p. 245-50., https://www.ncbi.nlm.nih.gov/pubmed/15710122
543. Wehner, MR, Linos, E, Parvataneni, R, Stuart, SE, Boscardin, WJ, Chren, MM, Timing of subsequent new tumors in patients who present with basal cell carcinoma or cutaneous squamous cell carcinoma., JAMA Dermatol, 2015. 151 (4)(4): p. 382-8., https://pubmed.ncbi.nlm.nih.gov/25588079/
544. Madeleine, MM, Patel, NS, Plasmeijer, EI, Engels, EA, Bouwes Bavinck, JN, Toland, AE, et.al. Epidemiology of keratinocyte carcinomas after organ transplantation., Br J Dermatol, 2017. 177 (5)(5): p. 1208-1216., https://pubmed.ncbi.nlm.nih.gov/28994104/
545. Xing, Y., Bronstein, Y., Ross, M. I., Askew, R. L., Lee, J. E., Gershenwald, J. E., et.al. Contemporary diagnostic imaging modalities for the staging and surveillance of melanoma patients: a meta-analysis, J Natl Cancer Inst, 2011. 103(2): p. 129-42., https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022618/pdf/djq455.pdf
546. Bafounta, M. L., Beauchet, A., Chagnon, S., Saiag, P., Ultrasonography or palpation for detection of melanoma nodal invasion: a meta-analysis, Lancet Oncol, 2004. 5(11): p. 673-80., https://www.ncbi.nlm.nih.gov/pubmed/15522655
547. Sumi, Misa, Ohki, Masafumi, Nakamura, Takashi, Comparison of Sonography and CT for Differentiating Benign from Malignant Cervical Lymph Nodes in Patients with Squamous Cell Carcinoma of the Head and Neck, American Journal of Roentgenology, 2001. 176(4): p. 1019-1024., https://doi.org/10.2214/ajr.176.4.1761019
548. Richards, P. S., Peacock, T. E., The role of ultrasound in the detection of cervical lymph node metastases in clinically N0 squamous cell carcinoma of the head and neck, Cancer Imaging, 2007. 7(1): p. 167-178., http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151323/
549. Davis, S. D., CT evaluation for pulmonary metastases in patients with extrathoracic malignancy, Radiology, 1991. 180(1): p. 1-12., https://www.ncbi.nlm.nih.gov/pubmed/2052672
550. Hausmann, Daniel, Jochum, Susanne, Utikal, Jochen, Hoffmann, Richard Christian, Zechmann, Christian, Neff, Kurt Wolfgang, et.al. Comparison of the diagnostic accuracy of whole-body MRI and whole-body CT in stage III/IV malignant melanoma, JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2011. 9(3): p. 212-221., http://dx.doi.org/10.1111/j.1610-0387.2011.07614.x
551. Galloway, Thomas J., Morris, Christopher G., Mancuso, Anthony A., Amdur, Robert J., Mendenhall, William M., Impact of radiographic findings on prognosis for skin carcinoma with clinical perineural invasion, Cancer, 2005. 103(6): p. 1254-1257., http://dx.doi.org/10.1002/cncr.20913
552. Mendenhall, WM, Ferlito, A, Takes, RP, Bradford, CR, Corry, J, Fagan, JJ, et.al. Cutaneous head and neck basal and squamous cell carcinomas with perineural invasion., Oral Oncol, 2012. 48 (10)(10): p. 918-922., https://pubmed.ncbi.nlm.nih.gov/22425152/
553. Hao, Dr. Sheng-Po, Ng, Dr. Shu-Hang, Magnetic Resonance Imaging versus Clinical Palpation in Evaluating Cervical Metastasis from Head and Neck Cancer, Otolaryngology-Head and Neck Surgery, 2000. 123(3): p. 324-327., http://journals.sagepub.com/doi/abs/10.1067/mhn.2000.105252
554. Williams, Lorna Sohn, Mancuso, Anthony A., Mendenhall, William M., Perineural spread of cutaneous squamous and basal cell carcinoma: CT and MR detection and its impact on patient management and prognosis, International Journal of Radiation Oncology • Biology • Physics 49(4): p. 1061-1069., http://dx.doi.org/10.1016/S0360-3016(00)01407-3
555. Duncan, James Robert, Carr, David, Kaffenberger, Benjamin Harris, The utility of positron emission tomography with and without computed tomography in patients with nonmelanoma skin cancer, Journal of the American Academy of Dermatology, 2016. 75(1): p. 186-196., http://dx.doi.org/10.1016/j.jaad.2016.01.045
556. van der Leest, RJT, Hollestein, LM, Liu, L, Nijsten, T, de Vries, E, Risks of different skin tumour combinations after a first melanoma, squamous cell carcinoma and basal cell carcinoma in Dutch population-based cohorts: 1989-2009., J Eur Acad Dermatol Venereol, 2018. 32 (3)(3): p. 382-389., https://pubmed.ncbi.nlm.nih.gov/28898461/
557. Lau, AT, Li, M, Xie, R, He, QY, Chiu, JF, Opposed arsenite-induced signaling pathways promote cell proliferation or apoptosis in cultured lung cells., Carcinogenesis, 2004. 25 (1)(1): p. 21-8., https://pubmed.ncbi.nlm.nih.gov/14514659/
558. Neubauer, O., Arsenical cancer; a review., Br J Cancer, 1947. 1(2): p. 192 - 251.
559. Lichter, MD, Karagas, MR, Mott, LA, Spencer, SK, Stukel, TA, Greenberg, ER, Therapeutic ionizing radiation and the incidence of basal cell carcinoma and squamous cell carcinoma. The New Hampshire Skin Cancer Study Group., Arch Dermatol, 2000. 136 (8)(8): p. 1007-11., https://pubmed.ncbi.nlm.nih.gov/10926736/
560. Shore, RE, Radiation-induced skin cancer in humans., Med Pediatr Oncol, 2001. 36 (5)(5): p. 549-54., https://pubmed.ncbi.nlm.nih.gov/11340610/
561. Sugita, K, Yamamoto, O, Suenaga, Y, [Seven cases of radiation-induced cutaneous squamous cell carcinoma]., J UOEH, 2000. 22 (3)(3): p. 259-67., https://pubmed.ncbi.nlm.nih.gov/11019392/
562. Voelter-Mahlknecht, S, Scheriau, R, Zwahr, G, Koch, B, Escobar Pinzon, LC, Drexler, H, et.al. Skin tumors among employees of a tar refinery: the current data and their implications., Int Arch Occup Environ Health, 2007. 80 (6)(6): p. 485-95., https://pubmed.ncbi.nlm.nih.gov/17093963/
563. Bamberger Empfehlung, Empfehlung zur Begutachtung von arbeitsbedingten Hauterkrankungen und Hautkrebserkrankungen, 2017., https://publikationen.dguv.de/widgets/pdf/download/article/2058
564. Ärztliches Zentrum für Qualität in der Medizin (ÄZQ), Gramsch, E, Hoppe, JD, Jonitz, G, Köhler, A, Ollenschläger, G , et.al. Kompendium Q-M-A. Qualitätsmanagement in der ambulanten VersorgungDt. Ärzte-Verl., 2008.
565. Aerztliches Zentrum für Qualitaet in der Medizin (AeZQ), Manual Qualitaetsindikatoren. Manual für Autoren., 2009. aezq Schriftenreihe: 36:, http://www.aezq.de/mdb/edocs/pdf/schriftenreihe/schriftenreihe36.pdf