Leitlinienprogramm OnkologieSoft Tissue Sarcoma

16. Literaturverzeichnis – Soft Tissue Sarcoma

Version 1.1 · May 2022 · AWMF 032/044OL
Leitlinienprogramm Onkologie · Deutsche Krebsgesellschaft · Deutsche Krebshilfe · AWMF

1. Balshem, H., Helfand, M., Schunemann, H. J., Oxman, A. D., Kunz, R., Brozek, J., et.al. GRADE guidelines: 3. Rating the quality of evidence, J Clin Epidemiol, 2011. 64(4): p. 401-6., https://www.ncbi.nlm.nih.gov/pubmed/21208779

2. Guyatt, G. H., Oxman, A. D., Vist, G., Kunz, R., Brozek, J., Alonso-Coello, P., et.al. GRADE guidelines: 4. Rating the quality of evidence--study limitations (risk of bias), J Clin Epidemiol, 2011. 64(4): p. 407-15., https://www.ncbi.nlm.nih.gov/pubmed/21247734

3. Guyatt, G. H., Oxman, A. D., Kunz, R., Woodcock, J., Brozek, J., Helfand, M., et.al. GRADE guidelines: 7. Rating the quality of evidence--inconsistency, J Clin Epidemiol, 2011. 64(12): p. 1294-302., https://www.ncbi.nlm.nih.gov/pubmed/21803546

4. Guyatt, G. H., Oxman, A. D., Kunz, R., Woodcock, J., Brozek, J., Helfand, M., et.al. GRADE guidelines: 8. Rating the quality of evidence--indirectness, J Clin Epidemiol, 2011. 64(12): p. 1303-10., https://www.ncbi.nlm.nih.gov/pubmed/21802903

5. Guyatt, G. H., Oxman, A. D., Kunz, R., Brozek, J., Alonso-Coello, P., Rind, D., et.al. GRADE guidelines 6. Rating the quality of evidence--imprecision, J Clin Epidemiol, 2011. 64(12): p. 1283-93., https://www.ncbi.nlm.nih.gov/pubmed/21839614

6. Guyatt, G. H., Oxman, A. D., Montori, V., Vist, G., Kunz, R., Brozek, J., et.al. GRADE guidelines: 5. Rating the quality of evidence--publication bias, J Clin Epidemiol, 2011. 64(12): p. 1277-82., https://www.ncbi.nlm.nih.gov/pubmed/21802904

7. Guyatt, G. H., Oxman, A. D., Sultan, S., Glasziou, P., Akl, E. A., Alonso-Coello, P., et.al. GRADE guidelines: 9. Rating up the quality of evidence, J Clin Epidemiol, 2011. 64(12): p. 1311-6., https://www.ncbi.nlm.nih.gov/pubmed/21802902

8. Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften - Ständige Kommission, Leitlinien, AWMF-Regelwerk "Leitlinien", 1. Auflage 2012. 09.12.2013:, http://www.awmf.org/leitlinien/awmf-regelwerk/awmf-regelwerk.html

9. Lahat, G., Lazar, A., Lev, D., Sarcoma epidemiology and etiology: potential environmental and genetic factors, Surg Clin North Am, 2008. 88(3): p. 451-81, v., https://www.ncbi.nlm.nih.gov/pubmed/18514694

10. Burningham, Z., Hashibe, M., Spector, L., Schiffman, J. D., The epidemiology of sarcoma, Clin Sarcoma Res, 2012. 2(1): p. 14., https://www.ncbi.nlm.nih.gov/pubmed/23036164

11. Toro, J. R., Travis, L. B., Wu, H. J., Zhu, K., Fletcher, C. D., Devesa, S. S., Incidence patterns of soft tissue sarcomas, regardless of primary site, in the surveillance, epidemiology and end results program, 1978-2001: An analysis of 26,758 cases, Int J Cancer, 2006. 119(12): p. 2922-30., https://www.ncbi.nlm.nih.gov/pubmed/17013893

12. Stiller, C. A., Trama, A., Serraino, D., Rossi, S., Navarro, C., Chirlaque, M. D., et.al. Descriptive epidemiology of sarcomas in Europe: report from the RARECARE project, Eur J Cancer, 2013. 49(3): p. 684-95., https://www.ncbi.nlm.nih.gov/pubmed/23079473

13. Krebs in Deutschland 2013/2014Robert Koch-Institut (Hrsg) und die Gesellschaft der epidemiologischen Krebsregister in Deutschland e.V. (Hrsg), 2017, 11 Ausgabe.

14. Ressing, M., Wardelmann, E., Hohenberger, P., Jakob, J., Kasper, B., Emrich, K., et.al. Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany, BMC Public Health, 2018. 18(1): p. 235., https://www.ncbi.nlm.nih.gov/pubmed/29433465

15. Herzog, C. E., Overview of sarcomas in the adolescent and young adult population, J Pediatr Hematol Oncol, 2005. 27(4): p. 215-8., https://www.ncbi.nlm.nih.gov/pubmed/15838394

16. Wibmer, C., Leithner, A., Zielonke, N., Sperl, M., Windhager, R., Increasing incidence rates of soft tissue sarcomas? A population-based epidemiologic study and literature review, Ann Oncol, 2010. 21(5): p. 1106-11., https://www.ncbi.nlm.nih.gov/pubmed/19858086

17. Gage, M. M., Nagarajan, N., Ruck, J. M., Canner, J. K., Khan, S., Giuliano, K., et.al. Sarcomas in the United States: Recent trends and a call for improved staging, Oncotarget, 2019. 10(25): p. 2462-2474., https://www.ncbi.nlm.nih.gov/pubmed/31069009

18. Bahl, S., Theis, B., Nishri, D., Marrett, L. D., Changing incidence of AIDS-related Kaposi sarcoma and non-Hodgkin lymphoma in Ontario, Canada, Cancer Causes Control, 2008. 19(10): p. 1251-8., https://www.ncbi.nlm.nih.gov/pubmed/18618279

19. Hirota, S., Isozaki, K., Moriyama, Y., Hashimoto, K., Nishida, T., Ishiguro, S., et.al. Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors, Science, 1998. 279(5350): p. 577-80., https://www.ncbi.nlm.nih.gov/pubmed/9438854

20. Ma, G. L., Murphy, J. D., Martinez, M. E., Sicklick, J. K., Epidemiology of gastrointestinal stromal tumors in the era of histology codes: results of a population-based study, Cancer Epidemiol Biomarkers Prev, 2015. 24(1): p. 298-302., https://www.ncbi.nlm.nih.gov/pubmed/25277795

21. Lv, M., Wu, C., Zheng, Y., Zhao, N., Incidence and survival analysis of gastrointestinal stromal tumors in shanghai: a population-based study from 2001 to 2010, Gastroenterol Res Pract, 2014. 2014: p. 834136., https://www.ncbi.nlm.nih.gov/pubmed/24864136

22. Maretty-Nielsen, K., Aggerholm-Pedersen, N., Keller, J., Safwat, A., Baerentzen, S., Pedersen, A. B., Relative mortality in soft tissue sarcoma patients: a Danish population-based cohort study, BMC Cancer, 2014. 14: p. 682., https://www.ncbi.nlm.nih.gov/pubmed/25239186

23. Selik, R. M., Starcher, E. T., Curran, J. W., Opportunistic diseases reported in AIDS patients: frequencies, associations, and trends, AIDS, 1987. 1(3): p. 175-82., https://www.ncbi.nlm.nih.gov/pubmed/2831912

24. Bhatia, K., Shiels, M. S., Berg, A., Engels, E. A., Sarcomas other than Kaposi sarcoma occurring in immunodeficiency: interpretations from a systematic literature review, Curr Opin Oncol, 2012. 24(5): p. 537-46., https://www.ncbi.nlm.nih.gov/pubmed/22729152

25. Chang, Y., Cesarman, E., Pessin, M. S., Lee, F., Culpepper, J., Knowles, D. M., et.al. Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi's sarcoma, Science, 1994. 266(5192): p. 1865-9., https://www.ncbi.nlm.nih.gov/pubmed/7997879

26. Moore, P. S., Chang, Y., Detection of herpesvirus-like DNA sequences in Kaposi's sarcoma in patients with and those without HIV infection, N Engl J Med, 1995. 332(18): p. 1181-5., https://www.ncbi.nlm.nih.gov/pubmed/7700310

27. Hatano, M., Takada, H., Nomura, A., Ohga, S., Ohshima, K., Saeki, I., et.al. Epstein-Barr virus-associated bronchial leiomyoma in a boy with cellular immunodeficiency, Pediatr Pulmonol, 2006. 41(4): p. 371-3., https://www.ncbi.nlm.nih.gov/pubmed/16429426

28. Fernandez, M. P., Krejci-Manwaring, J., Davis, T. L., Epstein-Barr virus is not associated with angioleiomyomas, or other cutaneous smooth muscle tumors in immunocompetent individuals, J Cutan Pathol, 2010. 37(4): p. 507-10., https://www.ncbi.nlm.nih.gov/pubmed/19615017

29. Stubbins, R. J., Alami Laroussi, N., Peters, A. C., Urschel, S., Dicke, F., Lai, R. L., et.al. Epstein-Barr virus associated smooth muscle tumors in solid organ transplant recipients: Incidence over 31 years at a single institution and review of the literature, Transpl Infect Dis, 2019. 21(1): p. e13010., https://www.ncbi.nlm.nih.gov/pubmed/30298678

30. Cohen, J. I., Dropulic, L., Hsu, A. P., Zerbe, C. S., Krogmann, T., Dowdell, K., et.al. Association of GATA2 Deficiency With Severe Primary Epstein-Barr Virus (EBV) Infection and EBV-associated Cancers, Clin Infect Dis, 2016. 63(1): p. 41-7., https://www.ncbi.nlm.nih.gov/pubmed/27169477

31. Monforte-Munoz, H., Kapoor, N., Saavedra, J. A., Epstein-Barr virus-associated leiomyomatosis and posttransplant lymphoproliferative disorder in a child with severe combined immunodeficiency: case report and review of the literature, Pediatr Dev Pathol, 2003. 6(5): p. 449-57., https://www.ncbi.nlm.nih.gov/pubmed/14708738

32. Rubino, C., Shamsaldin, A., Le, M. G., Labbe, M., Guinebretiere, J. M., Chavaudra, J., et.al. Radiation dose and risk of soft tissue and bone sarcoma after breast cancer treatment, Breast Cancer Res Treat, 2005. 89(3): p. 277-88., https://www.ncbi.nlm.nih.gov/pubmed/15754127

33. Virtanen, A., Pukkala, E., Auvinen, A., Incidence of bone and soft tissue sarcoma after radiotherapy: a cohort study of 295,712 Finnish cancer patients, Int J Cancer, 2006. 118(4): p. 1017-21., https://www.ncbi.nlm.nih.gov/pubmed/16152578

34. Menu-Branthomme, A., Rubino, C., Shamsaldin, A., Hawkins, M. M., Grimaud, E., Dondon, M. G., et.al. Radiation dose, chemotherapy and risk of soft tissue sarcoma after solid tumours during childhood, Int J Cancer, 2004. 110(1): p. 87-93., https://www.ncbi.nlm.nih.gov/pubmed/15054872

35. Jenkinson, H. C., Winter, D. L., Marsden, H. B., Stovall, M. A., Stevens, M. C., Stiller, C. A., et.al. A study of soft tissue sarcomas after childhood cancer in Britain, Br J Cancer, 2007. 97(5): p. 695-9., https://www.ncbi.nlm.nih.gov/pubmed/17653071

36. MacCarthy, A., Bayne, A. M., Brownbill, P. A., Bunch, K. J., Diggens, N. L., Draper, G. J., et.al. Second and subsequent tumours among 1927 retinoblastoma patients diagnosed in Britain 1951-2004, Br J Cancer, 2013. 108(12): p. 2455-63., https://www.ncbi.nlm.nih.gov/pubmed/23674091

37. Farzaliyev, F., Hamacher, R., Steinau Professor, H. U., Bertram, S., Podleska, L. E., Secondary angiosarcoma: A fatal complication of chronic lymphedema, J Surg Oncol, 2020. 121(1): p. 85-90., https://www.ncbi.nlm.nih.gov/pubmed/31236970

38. Shavit, E., Alavi, A., Limacher, J. J., Sibbald, R. G., Angiosarcoma complicating lower leg elephantiasis in a male patient: An unusual clinical complication, case report and literature review, SAGE Open Med Case Rep, 2018. 6: p. 2050313X18796343., https://www.ncbi.nlm.nih.gov/pubmed/30397474

39. Lipshutz, G. S., Brennan, T. V., Warren, R. S., Thorotrast-induced liver neoplasia: a collective review, J Am Coll Surg, 2002. 195(5): p. 713-8., https://www.ncbi.nlm.nih.gov/pubmed/12437262

40. Coulier, B., Pierard, F., Gielen, I., Maldague, P., Hepatic angiosarcoma occurring 65 years after thorium dioxide (Thorotrast) exposure: imaging, surgical and histo- pathologic findings of a historical case, JBR-BTR, 2014. 97(4): p. 254-8., https://www.ncbi.nlm.nih.gov/pubmed/25603638

41. Pukkala, E., Martinsen, J. I., Lynge, E., Gunnarsdottir, H. K., Sparen, P., Tryggvadottir, L., et.al. Occupation and cancer - follow-up of 15 million people in five Nordic countries, Acta Oncol, 2009. 48(5): p. 646-790., https://www.ncbi.nlm.nih.gov/pubmed/19925375

42. Hoppin, J. A., Tolbert, P. E., Flanders, W. D., Zhang, R. H., Daniels, D. S., Ragsdale, B. D., et.al. Occupational risk factors for sarcoma subtypes, Epidemiology, 1999. 10(3): p. 300-6., https://www.ncbi.nlm.nih.gov/pubmed/10230842

43. Mundt, K. A., Dell, L. D., Crawford, L., Gallagher, A. E., Quantitative estimated exposure to vinyl chloride and risk of angiosarcoma of the liver and hepatocellular cancer in the US industry-wide vinyl chloride cohort: mortality update through 2013, Occup Environ Med, 2017. 74(10): p. 709-716., https://www.ncbi.nlm.nih.gov/pubmed/28490663

44. Zahm, S. H., Blair, A., Holmes, F. F., Boysen, C. D., Robel, R. J., Fraumeni, J. F., Jr., A case-control study of soft-tissue sarcoma, Am J Epidemiol, 1989. 130(4): p. 665-74., https://www.ncbi.nlm.nih.gov/pubmed/2773915

45. Serraino, D., Franceschi, S., Talamini, R., Frustaci, S., La Vecchia, C., Non-occupational risk factors for adult soft-tissue sarcoma in northern Italy, Cancer Causes Control, 1991. 2(3): p. 157-64., https://www.ncbi.nlm.nih.gov/pubmed/1873445

46. Jouenne, F., Chauvot de Beauchene, I., Bollaert, E., Avril, M. F., Caron, O., Ingster, O., et.al. Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma, J Med Genet, 2017. 54(9): p. 607-612., https://www.ncbi.nlm.nih.gov/pubmed/28592523

47. Schneider, K., Zelley, K., Nichols, K. E., Garber, J., Li-Fraumeni Syndrome, in GeneReviews((R)), Adam, M. P.Ardinger, H. H.Pagon, R. A.Wallace, S. E.Bean, L. J. H.Mirzaa, G. and Amemiya, A., Editors. 1993: Seattle (WA)., https://www.ncbi.nlm.nih.gov/pubmed/20301488

48. von Mehren, M., Randall, R. L., Benjamin, R. S., Boles, S., Bui, M. M., Casper, E. S., et.al. Soft tissue sarcoma, version 2.2014, J Natl Compr Canc Netw, 2014. 12(4): p. 473-83., https://www.ncbi.nlm.nih.gov/pubmed/24717567

49. Ognjanovic, S., Olivier, M., Bergemann, T. L., Hainaut, P., Sarcomas in TP53 germline mutation carriers: a review of the IARC TP53 database, Cancer, 2012. 118(5): p. 1387-96., https://www.ncbi.nlm.nih.gov/pubmed/21837677

50. Mai, P. L., Best, A. F., Peters, J. A., DeCastro, R. M., Khincha, P. P., Loud, J. T., et.al. Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort, Cancer, 2016. 122(23): p. 3673-3681., https://www.ncbi.nlm.nih.gov/pubmed/27496084

51. Kleihues, P., Schauble, B., zur Hausen, A., Esteve, J., Ohgaki, H., Tumors associated with p53 germline mutations: a synopsis of 91 families, Am J Pathol, 1997. 150(1): p. 1-13., https://www.ncbi.nlm.nih.gov/pubmed/9006316

52. Ognjanovic, S., Martel, G., Manivel, C., Olivier, M., Langer, E., Hainaut, P., Low Prevalence of TP53 Mutations and MDM2 Amplifications in Pediatric Rhabdomyosarcoma, Sarcoma, 2012. 2012: p. 492086., https://www.ncbi.nlm.nih.gov/pubmed/22550420

53. Doros, L., Yang, J., Dehner, L., Rossi, C. T., Skiver, K., Jarzembowski, J. A., et.al. DICER1 mutations in embryonal rhabdomyosarcomas from children with and without familial PPB-tumor predisposition syndrome, Pediatr Blood Cancer, 2012. 59(3): p. 558-60., https://www.ncbi.nlm.nih.gov/pubmed/22180160

54. Diller, L., Sexsmith, E., Gottlieb, A., Li, F. P., Malkin, D., Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma, J Clin Invest, 1995. 95(4): p. 1606-11., https://www.ncbi.nlm.nih.gov/pubmed/7706467

55. Hettmer, S., Archer, N. M., Somers, G. R., Novokmet, A., Wagers, A. J., Diller, L., et.al. Anaplastic rhabdomyosarcoma in TP53 germline mutation carriers, Cancer, 2014. 120(7): p. 1068-75., https://www.ncbi.nlm.nih.gov/pubmed/24382691

56. Wang, W. L., Nero, C., Pappo, A., Lev, D., Lazar, A. J., Lopez-Terrada, D., CTNNB1 genotyping and APC screening in pediatric desmoid tumors: a proposed algorithm, Pediatr Dev Pathol, 2012. 15(5): p. 361-7., https://www.ncbi.nlm.nih.gov/pubmed/22372443

57. Kattentidt Mouravieva, A. A., Geurts-Giele, I. R., de Krijger, R. R., van Noesel, M. M., van de Ven, C. P., van den Ouweland, A. M., et.al. Identification of Familial Adenomatous Polyposis carriers among children with desmoid tumours, Eur J Cancer, 2012. 48(12): p. 1867-74., https://www.ncbi.nlm.nih.gov/pubmed/22305464

58. Brueckl, W. M., Ballhausen, W. G., Fortsch, T., Gunther, K., Fiedler, W., Gentner, B., et.al. Genetic testing for germline mutations of the APC gene in patients with apparently sporadic desmoid tumors but a family history of colorectal carcinoma, Dis Colon Rectum, 2005. 48(6): p. 1275-81., https://www.ncbi.nlm.nih.gov/pubmed/15793634

59. Farid, M., Ngeow, J., Sarcomas Associated With Genetic Cancer Predisposition Syndromes: A Review, Oncologist, 2016. 21(8): p. 1002-13., https://www.ncbi.nlm.nih.gov/pubmed/27401891

60. Bottillo, I., Ahlquist, T., Brekke, H., Danielsen, S. A., van den Berg, E., Mertens, F., et.al. Germline and somatic NF1 mutations in sporadic and NF1-associated malignant peripheral nerve sheath tumours, J Pathol, 2009. 217(5): p. 693-701., https://www.ncbi.nlm.nih.gov/pubmed/19142971

61. Upadhyaya, M., Spurlock, G., Monem, B., Thomas, N., Friedrich, R. E., Kluwe, L., et.al. Germline and somatic NF1 gene mutations in plexiform neurofibromas, Hum Mutat, 2008. 29(8): p. E103-11., https://www.ncbi.nlm.nih.gov/pubmed/18484666

62. Crucis, A., Richer, W., Brugieres, L., Bergeron, C., Marie-Cardine, A., Stephan, J. L., et.al. Rhabdomyosarcomas in children with neurofibromatosis type I: A national historical cohort, Pediatr Blood Cancer, 2015. 62(10): p. 1733-8., https://www.ncbi.nlm.nih.gov/pubmed/25893277

63. Postow, M. A., Robson, M. E., Inherited gastrointestinal stromal tumor syndromes: mutations, clinical features, and therapeutic implications, Clin Sarcoma Res, 2012. 2(1): p. 16., https://www.ncbi.nlm.nih.gov/pubmed/23036227

64. Pantaleo, M. A., Astolfi, A., Urbini, M., Nannini, M., Paterini, P., Indio, V., et.al. Analysis of all subunits, SDHA, SDHB, SDHC, SDHD, of the succinate dehydrogenase complex in KIT/PDGFRA wild-type GIST, Eur J Hum Genet, 2014. 22(1): p. 32-9., https://www.ncbi.nlm.nih.gov/pubmed/23612575

65. Boikos, S. A., Pappo, A. S., Killian, J. K., LaQuaglia, M. P., Weldon, C. B., George, S., et.al. Molecular Subtypes of KIT/PDGFRA Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Gastrointestinal Stromal Tumor Clinic, JAMA Oncol, 2016. 2(7): p. 922-8., https://www.ncbi.nlm.nih.gov/pubmed/27011036

66. Bachet, J. B., Emile, J. F., Diagnostic criteria, specific mutations, and genetic predisposition in gastrointestinal stromal tumors, Appl Clin Genet, 2010. 3: p. 85-101., https://www.ncbi.nlm.nih.gov/pubmed/23776354

67. Kleinerman, R. A., Schonfeld, S. J., Tucker, M. A., Sarcomas in hereditary retinoblastoma, Clin Sarcoma Res, 2012. 2(1): p. 15., https://www.ncbi.nlm.nih.gov/pubmed/23036192

68. Francis, J. H., Kleinerman, R. A., Seddon, J. M., Abramson, D. H., Increased risk of secondary uterine leiomyosarcoma in hereditary retinoblastoma, Gynecol Oncol, 2012. 124(2): p. 254-9., https://www.ncbi.nlm.nih.gov/pubmed/22027510

69. Wu, M. K., Vujanic, G. M., Fahiminiya, S., Watanabe, N., Thorner, P. S., O'Sullivan, M. J., et.al. Anaplastic sarcomas of the kidney are characterized by DICER1 mutations, Mod Pathol, 2018. 31(1): p. 169-178., https://www.ncbi.nlm.nih.gov/pubmed/28862265

70. Dehner, L. P., Jarzembowski, J. A., Hill, D. A., Embryonal rhabdomyosarcoma of the uterine cervix: a report of 14 cases and a discussion of its unusual clinicopathological associations, Mod Pathol, 2012. 25(4): p. 602-14., https://www.ncbi.nlm.nih.gov/pubmed/22157934

71. Yang, X. R., Ng, D., Alcorta, D. A., Liebsch, N. J., Sheridan, E., Li, S., et.al. T (brachyury) gene duplication confers major susceptibility to familial chordoma, Nat Genet, 2009. 41(11): p. 1176-8., https://www.ncbi.nlm.nih.gov/pubmed/19801981

72. Urso, E., Agostini, M., Pucciarelli, S., Bedin, C., D'Angelo, E., Mescoli, C., et.al. Soft tissue sarcoma and the hereditary non-polyposis colorectal cancer (HNPCC) syndrome: formulation of an hypothesis, Mol Biol Rep, 2012. 39(10): p. 9307-10., https://www.ncbi.nlm.nih.gov/pubmed/22782591

73. Hettmer, S., Teot, L. A., Kozakewich, H., Werger, A. M., Davies, K. J., Fletcher, C. D., et.al. Myogenic tumors in nevoid Basal cell carcinoma syndrome, J Pediatr Hematol Oncol, 2015. 37(2): p. 147-9., https://www.ncbi.nlm.nih.gov/pubmed/24517962

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75. Young, M. A., Herlihy, A., Mitchell, G., Thomas, D. M., Ballinger, M., Tucker, K., et.al. The attitudes of people with sarcoma and their family towards genomics and incidental information arising from genetic research, Clin Sarcoma Res, 2013. 3(1): p. 11., https://www.ncbi.nlm.nih.gov/pubmed/23898988

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77. Villani, A., Shore, A., Wasserman, J. D., Stephens, D., Kim, R. H., Druker, H., et.al. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study, Lancet Oncol, 2016. 17(9): p. 1295-305., https://www.ncbi.nlm.nih.gov/pubmed/27501770

78. Villani, A., Tabori, U., Schiffman, J., Shlien, A., Beyene, J., Druker, H., et.al. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study, Lancet Oncol, 2011. 12(6): p. 559-67., https://www.ncbi.nlm.nih.gov/pubmed/21601526

79. Ballinger, M. L., Best, A., Mai, P. L., Khincha, P. P., Loud, J. T., Peters, J. A., et.al. Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis, JAMA Oncol, 2017. 3(12): p. 1634-1639., https://www.ncbi.nlm.nih.gov/pubmed/28772291

80. Stacchiotti, S., Frezza, A. M., Blay, J. Y., Baldini, E. H., Bonvalot, S., Bovee, Jvmg, et.al. Ultra-rare sarcomas: A consensus paper from the Connective Tissue Oncology Society community of experts on the incidence threshold and the list of entities, Cancer, 2021., https://www.ncbi.nlm.nih.gov/pubmed/33910263

81. Lahat, G., Madewell, J. E., Anaya, D. A., Qiao, W., Tuvin, D., Benjamin, R. S., et.al. Computed tomography scan-driven selection of treatment for retroperitoneal liposarcoma histologic subtypes, Cancer, 2009. 115(5): p. 1081-90., https://www.ncbi.nlm.nih.gov/pubmed/19156920

82. Holzapfel, K, Regler, J, Baum, T, Rechl, H, Specht, K, Haller, B, et.al. Local Staging of Soft-Tissue Sarcoma: Emphasis on Assessment of Neurovascular Encasement-Value of MR Imaging in 174 Confirmed Cases., Radiology, 2015. 275 (2)(2): p. 501-9., https://pubmed.ncbi.nlm.nih.gov/25584707/

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