Leitlinienprogramm OnkologieMammakarzinom

13. Literaturverzeichnis – Mammakarzinom

Version 5.1 · Juni 2026 · AWMF 032-045OL
Leitlinienprogramm Onkologie · Deutsche Krebsgesellschaft · Deutsche Krebshilfe · AWMF

1. Sørensen, K, Van den Broucke, S, Fullam, J, Doyle, G, Pelikan, J, Slonska, Z, et.al. Health literacy and public health: a systematic review and integration of definitions and models., BMC Public Health, 2012. 12 (): p. 80., https://pubmed.ncbi.nlm.nih.gov/22276600/

2. Sieber, W. J., Kaplan, R. M., Informed adherence: the need for shared medical decision making, Control Clin Trials, 2000. 21(5 Suppl): p. 233s-40s., https://www.ncbi.nlm.nih.gov/pubmed/11018581

3. Weinstein, James N, Editorial: The missing piece: Embracing shared decision making to reform health careLWW, 2000.

4. Wright, E. B., Holcombe, C., Salmon, P., Doctors' communication of trust, care, and respect in breast cancer: qualitative study, Bmj, 2004. 328(7444): p. 864., https://www.ncbi.nlm.nih.gov/pubmed/15054034

5. Gysels, M., Higginson, I. J., Interactive technologies and videotapes for patient education in cancer care: systematic review and meta-analysis of randomised trials, Support Care Cancer, 2007. 15(1): p. 7-20., https://www.ncbi.nlm.nih.gov/pubmed/17024500

6. Wofford, J. L., Smith, E. D., Miller, D. P., The multimedia computer for office-based patient education: a systematic review, Patient Educ Couns, 2005. 59(2): p. 148-57., https://www.ncbi.nlm.nih.gov/pubmed/16257619

7. Beauchamp, Tom L, Childress, James F, Principles of biomedical ethicsOxford University Press, USA, 2001.

8. Zheng, H, Yang, L, Hu, J, Yang, Y, Frequency and Influencing Factors of Shared Decision Making Among Breast Cancer Patients Receiving Surgery: A Systematic Review and Meta-Analysis., Clin Breast Cancer, 2023. 23 (1)(1): p. e20-e31., https://pubmed.ncbi.nlm.nih.gov/36357267/

9. Katz, S. J., Lantz, P. M., Janz, N. K., Fagerlin, A., Schwartz, K., Liu, L., et.al. Patient involvement in surgery treatment decisions for breast cancer, J Clin Oncol, 2005. 23(24): p. 5526-33., https://www.ncbi.nlm.nih.gov/pubmed/16110013

10. Wagner, Katja, Koller, M, Keil, Astrid, Trott, Diana, Engenhart-Cabillic, Rita, Pfab, R, et.al. Strahlentherapie bei chirurgischen und nichtchirurgischen Patienten Therapieerwartungen, Lebensqualität und Arzteinschätzungen, Der Chirurg, 1998. 69(3): p. 252-258., https://pubmed.ncbi.nlm.nih.gov/9576035/

11. Weis, J., Giesler, J. M., Subjective dimensions of patient competence: relationships with selected healthcare usage behaviors and general features of self-rated competence, Patient Educ Couns, 2008. 73(3): p. 511-8., https://www.ncbi.nlm.nih.gov/pubmed/18952394

12. Albert, U-S, Koller, M, Wagner, U, Schulz, K-D, Survival chances and psychological aspects of quality of life in patients with localized early stage breast cancer, Inflammation Research, 2004. 53: p. S136-S141., https://www.ncbi.nlm.nih.gov/pubmed/15338065

13. Wildiers, H., Heeren, P., Puts, M., Topinkova, E., Janssen-Heijnen, M. L., Extermann, M., et.al. International Society of Geriatric Oncology consensus on geriatric assessment in older patients with cancer, J Clin Oncol, 2014. 32(24): p. 2595-603., https://www.ncbi.nlm.nih.gov/pubmed/25071125

14. Chouliara, Z., Kearney, N., Stott, D., Molassiotis, A., Miller, M., Perceptions of older people with cancer of information, decision making and treatment: a systematic review of selected literature, Ann Oncol, 2004. 15(11): p. 1596-602., https://www.ncbi.nlm.nih.gov/pubmed/15520059

15. Hagerty, R. G., Butow, P. N., Ellis, P. M., Dimitry, S., Tattersall, M. H., Communicating prognosis in cancer care: a systematic review of the literature, Ann Oncol, 2005. 16(7): p. 1005-53., https://www.ncbi.nlm.nih.gov/pubmed/15939716

16. Kautz-Freimuth, S, Redaèlli, M, Shukri, A, Kentenich, H, Simic, D, Mildenberger, V, et.al. Effectiveness of evidence-based decision aids for women with pathogenic BRCA1 or BRCA2 variants in the german health care context: results from a randomized controlled trial., BMC Med Inform Decis Mak, 2023. 23 (1)(1): p. 223., https://pubmed.ncbi.nlm.nih.gov/37845719/

17. Gilligan, T, Coyle, N, Frankel, RM, Berry, DL, Bohlke, K, Epstein, RM, et.al. Patient-Clinician Communication: American Society of Clinical Oncology Consensus Guideline., J Clin Oncol, 2017. 35 (31)(31): p. 3618-3632., https://pubmed.ncbi.nlm.nih.gov/28892432/

18. Nicholas Zdenkowski, , Butow, P, Tesson, S, Boyle, F, A systematic review of decision aids for patients making a decision about treatment for early breast cancer., Breast, 2016. 26 (): p. 31-45., https://pubmed.ncbi.nlm.nih.gov/27017240/

19. Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG), HTA-Bericht Behandlungsgespräche: Führt eine gemeinsame Entscheidungsfindung von Arzt und Patient bei der Therapiewahl zu besseren Ergebnissen? Projekt: HT22-01, 06.09.2023., https://www.iqwig.de/presse/pressemitteilungen/pressemitteilungen-detailseite_100418.html

20. Runowicz, Carolyn D, Leach, Corinne R, Henry, N Lynn, Henry, Karen S, Mackey, Heather T, Cowens‐Alvarado, Rebecca L, et.al. American Cancer society/American society of clinical oncology breast Cancer survivorship care guideline, CA: a cancer journal for clinicians, 2016. 66(1): p. 43-73., https://pubmed.ncbi.nlm.nih.gov/26641959/

21. Leitlinienprogramm Onkologie (Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF), S3-Leitlinie Psychoonkologische Diagnostik, Beratung und Behandlung von erwachsenen Krebspatient*innen, Version 2.1, 2023. AWMF-Registernummer: 032-051OL:, https://www.leitlinienprogramm-onkologie.de/leitlinien/psychoonkologie

22. Wanchai, A, Anderson, EA, Armer, JM, A systematic review of m-health apps on managing side effects of breast cancer treatment., Support Care Cancer, 2022. 31 (1)(1): p. 86., https://pubmed.ncbi.nlm.nih.gov/36574048/

23. Singleton, AC, Raeside, R, Hyun, KK, Partridge, SR, Di Tanna, GL, Hafiz, N, et.al. Electronic Health Interventions for Patients With Breast Cancer: Systematic Review and Meta-Analyses., J Clin Oncol, 2022. 40 (20)(20): p. 2257-2270., https://pubmed.ncbi.nlm.nih.gov/35500200/

24. Horn, A, Jírů-Hillmann, S, Widmann, J, Montellano, FA, Salmen, J, Pryss, R, et.al. Systematic review on the effectiveness of mobile health applications on mental health of breast cancer survivors., J Cancer Surviv, 2023. ():, https://pubmed.ncbi.nlm.nih.gov/37906420/

25. Stock, S, Isselhard, A, Jünger, S, Peters, S, Schneider, G, Haarig, F, et.al. [DNVF Memorandum Health Literacy (Part 2) - Operationalisation and Measuring of Health Literacy from a Health Services Research Perspective]., Gesundheitswesen, 2022. 84 (4)(4): p. e26-e41., https://pubmed.ncbi.nlm.nih.gov/35472769/

27. (ECIBC), European Commission Initiative on Breast Cancer, Evidencereport update, 2016., http://ecibc.jrc.ec.europa.eu/recommendations/list/3

28. Organization, World Health, WHO position paper on mammography screeningWorld Health Organization, 2014., https://pubmed.ncbi.nlm.nih.gov/25642524/

29. Broeders, M., Moss, S., Nystrom, L., Njor, S., Jonsson, H., Paap, E., et.al. The impact of mammographic screening on breast cancer mortality in Europe: a review of observational studies, J Med Screen, 2012. 19 Suppl 1: p. 14-25., https://pubmed.ncbi.nlm.nih.gov/22972807/

30. (IARC)., International Agency for Research on Cancer, Breast Cancer Screening. IARC Handbook of Cancer Prevention., 2016. 15:, http://publications.iarc.fr/Book-And-Report-Series/Iarc-Handbooks-Of-Cancer-Prevention/Breast-Cancer-Screening-2016

31. Siu, A. L., Screening for Breast Cancer: U.S. Preventive Services Task Force Recommendation Statement, Ann Intern Med, 2016. 164(4): p. 279-96., https://www.ncbi.nlm.nih.gov/pubmed/26757170

33. Lauby-Secretan, B., Scoccianti, C., Loomis, D., Benbrahim-Tallaa, L., Bouvard, V., Bianchini, F., et.al. Breast-cancer screening--viewpoint of the IARC Working Group, N Engl J Med, 2015. 372(24): p. 2353-8., https://www.ncbi.nlm.nih.gov/pubmed/26039523

34. Wolf, AMD, Oeffinger, KC, Shih, TY, Walter, LC, Church, TR, Fontham, ETH, et.al. Screening for lung cancer: 2023 guideline update from the American Cancer Society., CA Cancer J Clin, 2024. 74 (1)(1): p. 50-81., https://pubmed.ncbi.nlm.nih.gov/37909877/

35. Trentham-Dietz, A, Chapman, CH, Jayasekera, J, Lowry, KP, Heckman-Stoddard, BM, Hampton, JM, et.al. Collaborative Modeling to Compare Different Breast Cancer Screening Strategies: A Decision Analysis for the US Preventive Services Task Force., JAMA, 2024. 331 (22)(22): p. 1947-1960., https://pubmed.ncbi.nlm.nih.gov/38687505/

36. Braun, B, Khil, L, Tio, J, Krause-Bergmann, B, Fuhs, A, Heidinger, O, et.al. Differences in Breast Cancer Characteristics by Mammography Screening Participation or Non-Participation., Dtsch Arztebl Int, 2018. 115 (31-32)(31-32): p. 520-527., https://pubmed.ncbi.nlm.nih.gov/30149831/

37. Tabár, L, Dean, PB, Chen, TH, Yen, AM, Chen, SL, Fann, JC, et.al. The incidence of fatal breast cancer measures the increased effectiveness of therapy in women participating in mammography screening., Cancer, 2019. 125 (4)(4): p. 515-523., https://pubmed.ncbi.nlm.nih.gov/30411328/

38. Trocchi, P, Kuss, O, Kääb-Sanyal, V, Heidinger, O, Stang, A, Trends in surgical treatment for breast cancer in Germany after the implementation of the mammography screening program., Eur J Epidemiol, 2019. 34 (12)(12): p. 1143-1150., https://pubmed.ncbi.nlm.nih.gov/31650416/

39. Zorzi, M, Puliti, D, Vettorazzi, M, De Lisi, V, Falcini, F, Federico, M, et.al. Mastectomy rates are decreasing in the era of service screening: a population-based study in Italy (1997-2001)., Br J Cancer, 2006. 95 (9)(9): p. 1265-8., https://pubmed.ncbi.nlm.nih.gov/17043685/

40. Jahresbericht Evaluation 2021, Deutsches Mammographie-Screening-Programm.Kooperationsgemeinschaft Mammographie, November 2023.

41. Carter, JL, Coletti, RJ, Harris, RP, Quantifying and monitoring overdiagnosis in cancer screening: a systematic review of methods., BMJ, 2015. 350 (): p. g7773., https://pubmed.ncbi.nlm.nih.gov/25569206/

42. Lauby-Secretan, B, Loomis, D, Straif, K, Breast-Cancer Screening--Viewpoint of the IARC Working Group., N Engl J Med, 2015. 373 (15)(15): p. 1479., https://pubmed.ncbi.nlm.nih.gov/26444742/

43. Myers, E. R., Moorman, P., Gierisch, J. M., Havrilesky, L. J., Grimm, L. J., Ghate, S., et.al. Benefits and Harms of Breast Cancer Screening: A Systematic Review, Jama, 2015. 314(15): p. 1615-34., https://www.ncbi.nlm.nih.gov/pubmed/26501537

44. Perry, N., Broeders, M., de Wolf, C., Tornberg, S., Holland, R., von Karsa, L., European guidelines for quality assurance in breast cancer screening and diagnosis. Fourth edition--summary document, Ann Oncol, 2008. 19(4): p. 614-22., https://www.ncbi.nlm.nih.gov/pubmed/18024988

45. Heywang-Köbrunner, SH, Schreer, I, Hacker, A, Noftz, MR, Katalinic, A, Conclusions for mammography screening after 25-year follow-up of the Canadian National Breast Cancer Screening Study (CNBSS)., Eur Radiol, 2016. 26 (2)(2): p. 342-50., https://pubmed.ncbi.nlm.nih.gov/26017741/

46. Gemeinsamer Bundesausschuss, Krebsfrüherkennungs-Richtlinie, Richtlinie über die Früherkennung von Krebserkrankungen – KFE-RL, 2023. In Kraft getreten am: 01.07.2024:, https://www.g-ba.de/downloads/62-492-3478/KFE-RL_2023-09-21_iK-2024-07-01.pdf

47. Bundesamt der Justiz, Gesetz zum Schutz vor der schädlichen Wirkung ionisierender Strahlung (Strahlenschutzgesetz - StrlSchG), 2024., https://www.gesetze-im-internet.de/strlschg/__84.html

48. Albert, Ute Susann, Altland, H, Duda, V, Stufe-3-Leitlinie Brustkrebs-Früherkennung in DeutschlandZuckschwerdt München, 2008.

49. Group., Duke Evidence Synthesis, Systematic Review of Cancer Screening Literature for Updating American Cancer Society Breast Cancer Screening Guidelines.Duke Clinical Research Institute, Durham, NC: Guidelines Development Group, 2014., http://www.cancer.org/acs/groups/content/documents/document/acspc-046315.pdf

50. Organization, World Health, WHO position paper on mammography screeningWorld Health Organization, 2014., https://pubmed.ncbi.nlm.nih.gov/25642524/

51. Siu, A. L., Screening for Breast Cancer: U.S. Preventive Services Task Force Recommendation Statement, Ann Intern Med, 2016. 164(4): p. 279-96., https://www.ncbi.nlm.nih.gov/pubmed/26757170

52. (IARC)., International Agency for Research on Cancer, Breast Cancer Screening. IARC Handbook of Cancer Prevention., 2016. 15:, http://publications.iarc.fr/Book-And-Report-Series/Iarc-Handbooks-Of-Cancer-Prevention/Breast-Cancer-Screening-2016

53. Plevritis, SK, Munoz, D, Kurian, AW, Stout, NK, Alagoz, O, Near, AM, et.al. Association of Screening and Treatment With Breast Cancer Mortality by Molecular Subtype in US Women, 2000-2012., JAMA, 2018. 319 (2)(2): p. 154-164., https://pubmed.ncbi.nlm.nih.gov/29318276/

54. Pace, L. E., Keating, N. L., A systematic assessment of benefits and risks to guide breast cancer screening decisions, Jama, 2014. 311(13): p. 1327-35., https://www.ncbi.nlm.nih.gov/pubmed/24691608

55. Gemeinsamer Bundesausschuss, Mammographie-Screening -eine Entscheidungshilfe, 2023., https://www.g-ba.de/downloads/17-98-2232/2023-09-21_G-BA_Entscheidungshilfe_Mammographie_bf.pdf

56. Chen, TH, Yen, AM, Fann, JC, Gordon, P, Chen, SL, Chiu, SY, et.al. Clarifying the debate on population-based screening for breast cancer with mammography: A systematic review of randomized controlled trials on mammography with Bayesian meta-analysis and causal model., Medicine (Baltimore), 2017. 96 (3)(3): p. e5684., https://pubmed.ncbi.nlm.nih.gov/28099330/

57. Duffy, SW, Tabar, L, Chen, THH, Yen, AMF, Dean, PB, Smith, RA, A plea for more careful scholarship in reviewing evidence: the case of mammographic screening., BJR Open, 2023. 5 (1)(1): p. 20230041., https://pubmed.ncbi.nlm.nih.gov/37942497/

58. Nicholson, WK, Silverstein, M, Wong, JB, Barry, MJ, Chelmow, D, Coker, TR, et.al. Screening for Breast Cancer: US Preventive Services Task Force Recommendation Statement., JAMA, 2024. 331 (22)(22): p. 1918-1930., https://pubmed.ncbi.nlm.nih.gov/38687503/

59. Stout, NK, Miglioretti, DL, Su, YR, Lee, CI, Abraham, L, Alagoz, O, et.al. Breast Cancer Screening Using Mammography, Digital Breast Tomosynthesis, and Magnetic Resonance Imaging by Breast Density., JAMA Intern Med, 2024. 184 (10)(10): p. 1222-1231., https://pubmed.ncbi.nlm.nih.gov/39186304/

60. Hübner, J, Katalinic, A, Waldmann, A, Kraywinkel, K, Long-term Incidence and Mortality Trends for Breast Cancer in Germany., Geburtshilfe Frauenheilkd, 2020. 80 (6)(6): p. 611-618., https://pubmed.ncbi.nlm.nih.gov/32565551/

61. Katalinic, A, Eisemann, N, Kraywinkel, K, Noftz, MR, Hübner, J, Breast cancer incidence and mortality before and after implementation of the German mammography screening program., Int J Cancer, 2020. 147 (3)(3): p. 709-718., https://pubmed.ncbi.nlm.nih.gov/31675126/

62. bfs, Brustkrebsfrüherkennung mittels Röntgenmammographie bei Frauenab 70 Jahren Wissenschaftliche Bewertung des Bundesamtes für Strahlenschutz, Wissenschaftliche Bewertung des Bundesamtes für Strahlenschutz gemäß § 84 Absatz 3 Strahlenschutzgesetz, 2022., https://doris.bfs.de/jspui/bitstream/urn:nbn:de:0221-2022102634826/6/44-22-WissBericht_MSP70.pdf

63. IQWIG- Bericht 1383, Überprüfung der Altersgrenzen im Mammografie-Screening-Programm, 2022., https://www.iqwig.de/download/s21-01_altersgrenzen-im-mammografie-screening-programm_abschlussbericht_v1-1.pdf

64. Hölzel, D, Halfter, K, Schubert-Fritschle, G, Engel, J, Expanding mammography screening for women aged 40-80 years: evidence from a modeling approach using real-world data., Sci Rep, 2023. 13 (1)(1): p. 16229., https://pubmed.ncbi.nlm.nih.gov/37758770/

65. Canelo-Aybar, Carlos, Ferreira, Diogenes S, Ballesteros, Mónica, Posso, Margarita, Montero, Nadia, Solà, Ivan, et.al. Benefits and harms of breast cancer mammography screening for women at average risk of breast cancer: A systematic review for the European Commission Initiative on Breast CancerSAGE Publications, Journal of Medical Screening, 2021. 28(4): p. 389 - 404., https://doi.org/10.1177/0969141321993866

66. Moss, S. M., Wale, C., Smith, R., Evans, A., Cuckle, H., Duffy, S. W., Effect of mammographic screening from age 40 years on breast cancer mortality in the UK Age trial at 17 years' follow-up: a randomised controlled trial, Lancet Oncol, 2015. 16(9): p. 1123-32., https://www.ncbi.nlm.nih.gov/pubmed/26206144

67. bfs, Brustkrebsfrüherkennung mittels Röntgenmammographie bei Frauen unter 50 Jahren Wissenschaftliche Bewertung des Bundesamtes für Strahlenschutz gemäß § 84 Absatz 3 Strahlenschutzgesetz BfS-55/23, 2023., https://doris.bfs.de/jspui/bitstream/urn:nbn:de:0221-2023110840049/3/BfS-55-23.pdf

68. USPSTF Bulletin, Task Force Issues Final Recommendation Statement on Screening for Breast Cancer All women should be screened every other year starting at age 40, 30.04.2024., https://www.uspreventiveservicestaskforce.org/uspstf/sites/default/files/file/supporting_documents/breast-cancer-screening-final-rec-bulletin.pdf

69. Miglioretti, DL, Lange, J, van den Broek, JJ, Lee, CI, van Ravesteyn, NT, Ritley, D, et.al. Radiation-Induced Breast Cancer Incidence and Mortality From Digital Mammography Screening: A Modeling Study., Ann Intern Med, 2016. 164 (4)(4): p. 205-14., https://pubmed.ncbi.nlm.nih.gov/26756460/

70. National Institute for Health and Care Excellence (NICE), Familial breast cancer: classification, care and managing breast cancer and related risks in people with a family history of breast cancer, 2019. No. 164:, https://pubmed.ncbi.nlm.nih.gov/31940157/

71. Lee, A, Mavaddat, N, Wilcox, AN, Cunningham, AP, Carver, T, Hartley, S, et.al. BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors., Genet Med, 2019. 21 (8)(8): p. 1708-1718., https://pubmed.ncbi.nlm.nih.gov/30643217/

72. Hamad, W, Michell, MJ, Myles, JP, Gilbert, FJ, Chen, Y, Jin, H, et.al. Diagnostic performance of tomosynthesis plus synthetic mammography versus full-field digital mammography with or without tomosynthesis in breast cancer screening: A systematic review and meta-analysis., Int J Cancer, 2024. ():, https://pubmed.ncbi.nlm.nih.gov/39394862/

73. Heywang-Köbrunner, SH, Jänsch, A, Hacker, A, Weinand, S, Vogelmann, T, Digital breast tomosynthesis (DBT) plus synthesised two-dimensional mammography (s2D) in breast cancer screening is associated with higher cancer detection and lower recalls compared to digital mammography (DM) alone: results of a systematic review and meta-analysis., Eur Radiol, 2022. 32 (4)(4): p. 2301-2312., https://pubmed.ncbi.nlm.nih.gov/34694451/

74. Lin, H, Zhang, Y, Wu, L, Li, C, Diagnostic accuracy of digital breast tomosynthesis and digital mammography in women with dense or non-dense breast tissue: A systematic review and meta-analysis., Adv Clin Exp Med, 2024. ():, https://pubmed.ncbi.nlm.nih.gov/39087824/

75. Heindel, W, Weigel, S, Gerß, J, Hense, HW, Sommer, A, Krischke, M, et.al. Digital breast tomosynthesis plus synthesised mammography versus digital screening mammography for the detection of invasive breast cancer (TOSYMA): a multicentre, open-label, randomised, controlled, superiority trial., Lancet Oncol, 2022. 23 (5)(5): p. 601-611., https://pubmed.ncbi.nlm.nih.gov/35427470/

76. Alabousi, M, Wadera, A, Kashif Al-Ghita, M, Kashef Al-Ghetaa, R, Salameh, JP, Pozdnyakov, A, et.al. Performance of Digital Breast Tomosynthesis, Synthetic Mammography, and Digital Mammography in Breast Cancer Screening: A Systematic Review and Meta-Analysis., J Natl Cancer Inst, 2021. 113 (6)(6): p. 680-690., https://pubmed.ncbi.nlm.nih.gov/33372954/

77. Weigel, S, Heindel, W, Hense, HW, Decker, T, Gerß, J, Kerschke, L, Breast Density and Breast Cancer Screening with Digital Breast Tomosynthesis: A TOSYMA Trial Subanalysis., Radiology, 2023. 306 (2)(2): p. e221006., https://pubmed.ncbi.nlm.nih.gov/36194110/

78. Heywang-Köbrunner, SH, Jänsch, A, Hacker, A, Weinand, S, Vogelmann, T, Tomosynthesis with synthesised two-dimensional mammography yields higher cancer detection compared to digital mammography alone, also in dense breasts and in younger women: A systematic review and meta-analysis., Eur J Radiol, 2022. 152 (): p. 110324., https://pubmed.ncbi.nlm.nih.gov/35576720/

79. Li, T, Houssami, N, Noguchi, N, Zeng, A, Marinovich, ML, Differential detection by breast density for digital breast tomosynthesis versus digital mammography population screening: a systematic review and meta-analysis., Br J Cancer, 2022. 127 (1)(1): p. 116-125., https://pubmed.ncbi.nlm.nih.gov/35352019/

80. Libesman, S, Zackrisson, S, Hofvind, S, Seidler, AL, Bernardi, D, Lång, K, et.al. An individual participant data meta-analysis of breast cancer detection and recall rates for digital breast tomosynthesis versus digital mammography population screening., Clin Breast Cancer, 2022. 22 (5)(5): p. e647-e654., https://pubmed.ncbi.nlm.nih.gov/35246389/

81. Opitz, M, Zensen, S, Breuckmann, K, Bos, D, Forsting, M, Hoffmann, O, et.al. Breast Radiation Exposure of 3D Digital Breast Tomosynthesis Compared to Full-Field Digital Mammography in a Clinical Follow-Up Setting., Diagnostics (Basel), 2022. 12 (2)(2):, https://pubmed.ncbi.nlm.nih.gov/35204547/

82. Loveland, J, Mackenzie, A, Radiation doses received in the UK breast screening programmes 2019-2023., Br J Radiol, 2024. 97 (1156)(1156): p. 787-793., https://pubmed.ncbi.nlm.nih.gov/38291906/

83. Canelo-Aybar, C, Carrera, L, Beltrán, J, Posso, M, Rigau, D, Lebeau, A, et.al. Digital breast tomosynthesis compared to diagnostic mammographic projections (including magnification) among women recalled at screening mammography: a systematic review for the European Commission Initiative on Breast Cancer (ECIBC)., Cancer Med, 2021. 10 (7)(7): p. 2191-2204., https://pubmed.ncbi.nlm.nih.gov/33675147/

84. Houssami, N, Zackrisson, S, Blazek, K, Hunter, K, Bernardi, D, Lång, K, et.al. Meta-analysis of prospective studies evaluating breast cancer detection and interval cancer rates for digital breast tomosynthesis versus mammography population screening., Eur J Cancer, 2021. 148 (): p. 14-23., https://pubmed.ncbi.nlm.nih.gov/33706172/

85. Ohuchi, N, Suzuki, A, Sobue, T, Kawai, M, Yamamoto, S, Zheng, YF, et.al. Sensitivity and specificity of mammography and adjunctive ultrasonography to screen for breast cancer in the Japan Strategic Anti-cancer Randomized Trial (J-START): a randomised controlled trial., Lancet, 2016. 387 (10016)(10016): p. 341-348., https://pubmed.ncbi.nlm.nih.gov/26547101/

86. Harada-Shoji, N, Suzuki, A, Ishida, T, Zheng, YF, Narikawa-Shiono, Y, Sato-Tadano, A, et.al. Evaluation of Adjunctive Ultrasonography for Breast Cancer Detection Among Women Aged 40-49 Years With Varying Breast Density Undergoing Screening Mammography: A Secondary Analysis of a Randomized Clinical Trial., JAMA Netw Open, 2021. 4 (8)(8): p. e2121505., https://pubmed.ncbi.nlm.nih.gov/34406400/

87. Melnikow, J., Fenton, J. J., Whitlock, E. P., Miglioretti, D. L., Weyrich, M. S., Thompson, J. H., et.al. Supplemental Screening for Breast Cancer in Women With Dense Breasts: A Systematic Review for the U.S. Preventive Services Task Force, Ann Intern Med, 2016. 164(4): p. 268-78., https://www.ncbi.nlm.nih.gov/pubmed/26757021

88. Rebolj, M, Assi, V, Brentnall, A, Parmar, D, Duffy, SW, Addition of ultrasound to mammography in the case of dense breast tissue: systematic review and meta-analysis., Br J Cancer, 2018. 118 (12)(12): p. 1559-1570., https://pubmed.ncbi.nlm.nih.gov/29736009/

89. Yuan, WH, Hsu, HC, Chen, YY, Wu, CH, Supplemental breast cancer-screening ultrasonography in women with dense breasts: a systematic review and meta-analysis., Br J Cancer, 2020. 123 (4)(4): p. 673-688., https://pubmed.ncbi.nlm.nih.gov/32528118/

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773. Joseph, K, Vos, LJ, Gabos, Z, Pervez, N, Chafe, S, Tankel, K, et.al. Skin Toxicity in Early Breast Cancer Patients Treated with Field-In-Field Breast Intensity-Modulated Radiotherapy versus Helical Inverse Breast Intensity-Modulated Radiotherapy: Results of a Phase III Randomised Controlled Trial., Clin Oncol (R Coll Radiol), 2021. 33 (1)(1): p. 30-39., https://pubmed.ncbi.nlm.nih.gov/32711920/

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775. Fastner, G, Reitsamer, R, Gaisberger, C, Hitzl, W, Urbański, B, Murawa, D, et.al. Hypofractionated Whole Breast Irradiation and Boost-IOERT in Early Stage Breast Cancer (HIOB): First Clinical Results of a Prospective Multicenter Trial (NCT01343459)., Cancers (Basel), 2022. 14 (6)(6):, https://pubmed.ncbi.nlm.nih.gov/35326548/

776. Ciabattoni, A, Gregucci, F, Fastner, G, Cavuto, S, Spera, A, Drago, S, et.al. IOERT versus external beam electrons for boost radiotherapy in stage I/II breast cancer: 10-year results of a phase III randomized study., Breast Cancer Res, 2021. 23 (1)(1): p. 46., https://pubmed.ncbi.nlm.nih.gov/33849606/

777. Fastner, G, Reitsamer, R, Urbański, B, Kopp, P, Murawa, D, Adamczyk, B, et.al. Toxicity and cosmetic outcome after hypofractionated whole breast irradiation and boost-IOERT in early stage breast cancer (HIOB): First results of a prospective multicenter trial (NCT01343459)., Radiother Oncol, 2020. 146 (): p. 136-142., https://pubmed.ncbi.nlm.nih.gov/32151790/

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780. Ahn, SG, Bae, SJ, Lee, HW, Yoon, CI, Kim, JW, Lee, IJ, et.al. A phase II study investigating the acute toxicity of targeted intraoperative radiotherapy as tumor-bed boost plus whole breast irradiation after breast-conserving surgery in Korean patients., Breast Cancer Res Treat, 2019. 174 (1)(1): p. 157-163., https://pubmed.ncbi.nlm.nih.gov/30467660/

781. Sarria, GR, Ramos, ML, Palacios, A, Del Castillo, R, Castro, F, Calvo, A, et.al. Long-Term Outcomes of an International Cooperative Study of Intraoperative Radiotherapy Upfront Boost With Low Energy X-Rays in Breast Cancer., Front Oncol, 2022. 12 (): p. 850351., https://pubmed.ncbi.nlm.nih.gov/35371998/

782. Díaz-Gavela, AA, Cerro Peñalver, ED, Sanchez-Garcia, S, Pardo-Perez, E, Thuissard-Vasallo, IJ, Andreu-Vázquez, C, et.al. Hypofractionated whole breast IMRT with HDR brachytherapy boost in early-stage breast cancer: Long-term results from a single-center., Brachytherapy, 2024. 23 (3)(3): p. 342-354., https://pubmed.ncbi.nlm.nih.gov/38522961/

783. Strnad, V, Major, T, Polgar, C, Lotter, M, Guinot, JL, Gutierrez-Miguelez, C, et.al. ESTRO-ACROP guideline: Interstitial multi-catheter breast brachytherapy as Accelerated Partial Breast Irradiation alone or as boost - GEC-ESTRO Breast Cancer Working Group practical recommendations., Radiother Oncol, 2018. 128 (3)(3): p. 411-420., https://pubmed.ncbi.nlm.nih.gov/29691075/

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802. Offersen, BV, Alsner, J, Nielsen, HM, Jakobsen, EH, Nielsen, MH, Stenbygaard, L, et.al. Partial Breast Irradiation Versus Whole Breast Irradiation for Early Breast Cancer Patients in a Randomized Phase III Trial: The Danish Breast Cancer Group Partial Breast Irradiation Trial., J Clin Oncol, 2022. 40 (36)(36): p. 4189-4197., https://pubmed.ncbi.nlm.nih.gov/35930754/

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810. Shaitelman, SF, Anderson, BM, Arthur, DW, Bazan, JG, Bellon, JR, Bradfield, L, et.al. Partial Breast Irradiation for Patients With Early-Stage Invasive Breast Cancer or Ductal Carcinoma In Situ: An ASTRO Clinical Practice Guideline., Pract Radiat Oncol, 2024. 14 (2)(2): p. 112-132., https://pubmed.ncbi.nlm.nih.gov/37977261/

811. Anderson, B, Arthur, D, Hannoun-Levi, JM, Kamrava, M, Khan, A, Kuske, R, et.al. Partial breast irradiation: An updated consensus statement from the American brachytherapy society., Brachytherapy, 2022. 21 (6)(6): p. 726-747., https://pubmed.ncbi.nlm.nih.gov/36117086/

812. Strnad, V, Krug, D, Sedlmayer, F, Piroth, MD, Budach, W, Baumann, R, et.al. DEGRO practical guideline for partial-breast irradiation., Strahlenther Onkol, 2020. 196 (9)(9): p. 749-763., https://pubmed.ncbi.nlm.nih.gov/32350554/

813. Goldberg, M, Bridhikitti, J, Khan, AJ, McGale, P, Whelan, TJ, A Meta-Analysis of Trials of Partial Breast Irradiation., Int J Radiat Oncol Biol Phys, 2023. 115 (1)(1): p. 60-72., https://pubmed.ncbi.nlm.nih.gov/36155214/

814. Coles, CE, Griffin, CL, Kirby, AM, Titley, J, Agrawal, RK, Alhasso, A, et.al. Partial-breast radiotherapy after breast conservation surgery for patients with early breast cancer (UK IMPORT LOW trial): 5-year results from a multicentre, randomised, controlled, phase 3, non-inferiority trial., Lancet, 2017. 390 (10099)(10099): p. 1048-1060., https://pubmed.ncbi.nlm.nih.gov/28779963/

815. Meattini, I, Marrazzo, L, Saieva, C, Desideri, I, Scotti, V, Simontacchi, G, et.al. Accelerated Partial-Breast Irradiation Compared With Whole-Breast Irradiation for Early Breast Cancer: Long-Term Results of the Randomized Phase III APBI-IMRT-Florence Trial., J Clin Oncol, 2020. 38 (35)(35): p. 4175-4183., https://pubmed.ncbi.nlm.nih.gov/32840419/

816. Offersen, BV, Alsner, J, Nielsen, HM, Jakobsen, EH, Nielsen, MH, Stenbygaard, L, et.al. Partial Breast Irradiation Versus Whole Breast Irradiation for Early Breast Cancer Patients in a Randomized Phase III Trial: The Danish Breast Cancer Group Partial Breast Irradiation Trial., J Clin Oncol, 2022. 40 (36)(36): p. 4189-4197., https://pubmed.ncbi.nlm.nih.gov/35930754/

817. Strnad, V, Polgár, C, Ott, OJ, Hildebrandt, G, Kauer-Dorner, D, Knauerhase, H, et.al. Accelerated partial breast irradiation using sole interstitial multicatheter brachytherapy compared with whole-breast irradiation with boost for early breast cancer: 10-year results of a GEC-ESTRO randomised, phase 3, non-inferiority trial., Lancet Oncol, 2023. 24 (3)(3): p. 262-272., https://pubmed.ncbi.nlm.nih.gov/36738756/

818. Shaitelman, SF, Anderson, BM, Arthur, DW, Bazan, JG, Bellon, JR, Bradfield, L, et.al. Partial Breast Irradiation for Patients With Early-Stage Invasive Breast Cancer or Ductal Carcinoma In Situ: An ASTRO Clinical Practice Guideline., Pract Radiat Oncol, 2024. 14 (2)(2): p. 112-132., https://pubmed.ncbi.nlm.nih.gov/37977261/

819. Anderson, B, Arthur, D, Hannoun-Levi, JM, Kamrava, M, Khan, A, Kuske, R, et.al. Partial breast irradiation: An updated consensus statement from the American brachytherapy society., Brachytherapy, 2022. 21 (6)(6): p. 726-747., https://pubmed.ncbi.nlm.nih.gov/36117086/

820. Vaidya, JS, Bulsara, M, Baum, M, Wenz, F, Massarut, S, Pigorsch, S, et.al. Long term survival and local control outcomes from single dose targeted intraoperative radiotherapy during lumpectomy (TARGIT-IORT) for early breast cancer: TARGIT-A randomised clinical trial., BMJ, 2020. 370 (): p. m2836., https://pubmed.ncbi.nlm.nih.gov/32816842/

821. Vaidya, JS, Bulsara, M, Saunders, C, Flyger, H, Tobias, JS, Corica, T, et.al. Effect of Delayed Targeted Intraoperative Radiotherapy vs Whole-Breast Radiotherapy on Local Recurrence and Survival: Long-term Results From the TARGIT-A Randomized Clinical Trial in Early Breast Cancer., JAMA Oncol, 2020. 6 (7)(7): p. e200249., https://pubmed.ncbi.nlm.nih.gov/32239210/

822. Orecchia, R, Veronesi, U, Maisonneuve, P, Galimberti, VE, Lazzari, R, Veronesi, P, et.al. Intraoperative irradiation for early breast cancer (ELIOT): long-term recurrence and survival outcomes from a single-centre, randomised, phase 3 equivalence trial., Lancet Oncol, 2021. 22 (5)(5): p. 597-608., https://pubmed.ncbi.nlm.nih.gov/33845035/

823. Shumway, DA, Corbin, KS, Farah, MH, Viola, KE, Nayfeh, T, Saadi, S, et.al. Partial breast irradiation compared with whole breast irradiation: a systematic review and meta-analysis., J Natl Cancer Inst, 2023. 115 (9)(9): p. 1011-1019., https://pubmed.ncbi.nlm.nih.gov/37289549/

824. Polgár, C, Major, T, Takácsi-Nagy, Z, Fodor, J, Breast-Conserving Surgery Followed by Partial or Whole Breast Irradiation: Twenty-Year Results of a Phase 3 Clinical Study., Int J Radiat Oncol Biol Phys, 2021. 109 (4)(4): p. 998-1006., https://pubmed.ncbi.nlm.nih.gov/33186620/

825. Olivotto, IA, Whelan, TJ, Parpia, S, Kim, DH, Berrang, T, Truong, PT, et.al. Interim cosmetic and toxicity results from RAPID: a randomized trial of accelerated partial breast irradiation using three-dimensional conformal external beam radiation therapy., J Clin Oncol, 2013. 31 (32)(32): p. 4038-45., https://pubmed.ncbi.nlm.nih.gov/23835717/

826. McGale, P., Taylor, C., Correa, C., Cutter, D., Duane, F., Ewertz, M., et.al. Effect of radiotherapy after mastectomy and axillary surgery on 10-year recurrence and 20-year breast cancer mortality: meta-analysis of individual patient data for 8135 women in 22 randomised trials, Lancet, 2014. 383(9935): p. 2127-35., https://www.ncbi.nlm.nih.gov/pubmed/24656685

827. Gradishar, W. J., Anderson, B. O., Balassanian, R., Blair, S. L., Burstein, H. J., Cyr, A., et.al. Invasive Breast Cancer Version 1.2016, NCCN Clinical Practice Guidelines in Oncology, J Natl Compr Canc Netw, 2016. 14(3): p. 324-54., https://www.ncbi.nlm.nih.gov/pubmed/26957618

828. Wang, H., Kong, L., Zhang, C., Chen, D., Zhu, H., Yu, J., Should all breast cancer patients with four or more positive lymph nodes who underwent modified radical mastectomy be treated with postoperative radiotherapy? A population-based study, Oncotarget, 2016. 7(46): p. 75492-75502., https://www.ncbi.nlm.nih.gov/pubmed/27690343

829. Elmore, Leisha, Deshpande, Anjali, Daly, MacKenzie, Margenthaler, Julie A, Postmastectomy radiation therapy in T3 node-negative breast cancer, Journal of Surgical Research, 2015. 199(1): p. 90-96., https://www.ncbi.nlm.nih.gov/pubmed/25976852

830. Francis, S. R., Frandsen, J., Kokeny, K. E., Gaffney, D. K., Poppe, M. M., Outcomes and utilization of postmastectomy radiotherapy for T3N0 breast cancers, Breast, 2017. 32: p. 156-161., https://www.ncbi.nlm.nih.gov/pubmed/28193571

831. Karlsson, P., Cole, B. F., Chua, B. H., Price, K. N., Lindtner, J., Collins, J. P., et.al. Patterns and risk factors for locoregional failures after mastectomy for breast cancer: an International Breast Cancer Study Group report, Ann Oncol, 2012. 23(11): p. 2852-8., https://www.ncbi.nlm.nih.gov/pubmed/22776708

832. Kyndi, Marianne, Overgaard, Marie, Nielsen, Hanne M, Sørensen, Flemming B, Knudsen, Helle, Overgaard, Jens, High local recurrence risk is not associated with large survival reduction after postmastectomy radiotherapy in high-risk breast cancer: a subgroup analysis of DBCG 82 b&c, Radiotherapy and Oncology, 2009. 90(1): p. 74-79., https://pubmed.ncbi.nlm.nih.gov/18471914/

833. Nagao, T., Kinoshita, T., Tamura, N., Hojo, T., Morota, M., Kagami, Y., Locoregional recurrence risk factors in breast cancer patients with positive axillary lymph nodes and the impact of postmastectomy radiotherapy, Int J Clin Oncol, 2013. 18(1): p. 54-61., https://www.ncbi.nlm.nih.gov/pubmed/22068463

834. Nielsen, H. M., Overgaard, M., Grau, C., Jensen, A. R., Overgaard, J., Study of failure pattern among high-risk breast cancer patients with or without postmastectomy radiotherapy in addition to adjuvant systemic therapy: long-term results from the Danish Breast Cancer Cooperative Group DBCG 82 b and c randomized studies, J Clin Oncol, 2006. 24(15): p. 2268-75., https://www.ncbi.nlm.nih.gov/pubmed/16618947

835. Recht, A., Comen, E. A., Fine, R. E., Fleming, G. F., Hardenbergh, P. H., Ho, A. Y., et.al. Postmastectomy Radiotherapy: An American Society of Clinical Oncology, American Society for Radiation Oncology, and Society of Surgical Oncology Focused Guideline Update, J Clin Oncol, 2016. 34(36): p. 4431-4442., https://www.ncbi.nlm.nih.gov/pubmed/27646947

836. Wang, H., Zhang, C., Kong, L., Zhu, H., Yu, J., Better survival in PMRT of female breast cancer patients with >5 negative lymph nodes: A population-based study, Medicine (Baltimore), 2017. 96(4): p. e5998., https://www.ncbi.nlm.nih.gov/pubmed/28121956

837. Headon, Hannah, Kasem, Abdul, Almukbel, Reham, Mokbel, Kefah, Improvement of survival with postmastectomy radiotherapy in patients with 1-3 positive axillary lymph nodes: A systematic review and meta-analysis of the current literature, Molecular and Clinical Oncology, 2016. 5(4): p. 429-436., https://www.ncbi.nlm.nih.gov/pubmed/27699038

838. Valli, M. C., Controversies in loco-regional treatment: post-mastectomy radiation for pT2-pT3N0 breast cancer arguments in favour, Crit Rev Oncol Hematol, 2012. 84 Suppl 1: p. e70-4., https://www.ncbi.nlm.nih.gov/pubmed/21134765

839. Overgaard, M., Hansen, P. S., Overgaard, J., Rose, C., Andersson, M., Bach, F., et.al. Postoperative radiotherapy in high-risk premenopausal women with breast cancer who receive adjuvant chemotherapy. Danish Breast Cancer Cooperative Group 82b Trial, N Engl J Med, 1997. 337(14): p. 949-55., https://www.ncbi.nlm.nih.gov/pubmed/9395428

840. Overgaard, M., Jensen, M. B., Overgaard, J., Hansen, P. S., Rose, C., Andersson, M., et.al. Postoperative radiotherapy in high-risk postmenopausal breast-cancer patients given adjuvant tamoxifen: Danish Breast Cancer Cooperative Group DBCG 82c randomised trial, Lancet, 1999. 353(9165): p. 1641-8., https://www.ncbi.nlm.nih.gov/pubmed/10335782

841. Taghian, AG, Jeong, JH, Mamounas, EP, Parda, DS, Deutsch, M, Costantino, JP, et.al. Low locoregional recurrence rate among node-negative breast cancer patients with tumors 5 cm or larger treated by mastectomy, with or without adjuvant systemic therapy and without radiotherapy: results from five national surgical adjuvant breast and bowel project randomized clinical trials., J Clin Oncol, 2006. 24 (24)(24): p. 3927-32., https://pubmed.ncbi.nlm.nih.gov/16921044/

842. Taghian, A, Jeong, JH, Mamounas, E, Anderson, S, Bryant, J, Deutsch, M, et.al. Patterns of locoregional failure in patients with operable breast cancer treated by mastectomy and adjuvant chemotherapy with or without tamoxifen and without radiotherapy: results from five National Surgical Adjuvant Breast and Bowel Project randomized clinical trials., J Clin Oncol, 2004. 22 (21)(21): p. 4247-54., https://pubmed.ncbi.nlm.nih.gov/15452182/

843. Rusthoven, C. G., Rabinovitch, R. A., Jones, B. L., Koshy, M., Amini, A., Yeh, N., et.al. The impact of postmastectomy and regional nodal radiation after neoadjuvant chemotherapy for clinically lymph node-positive breast cancer: a National Cancer Database (NCDB) analysis, Ann Oncol, 2016. 27(5): p. 818-27., https://www.ncbi.nlm.nih.gov/pubmed/26861597

844. Mamounas, E. P., Anderson, S. J., Dignam, J. J., Bear, H. D., Julian, T. B., Geyer, C. E., Jr., et.al. Predictors of locoregional recurrence after neoadjuvant chemotherapy: results from combined analysis of National Surgical Adjuvant Breast and Bowel Project B-18 and B-27, J Clin Oncol, 2012. 30(32): p. 3960-6., https://www.ncbi.nlm.nih.gov/pubmed/23032615

845. Kishan, A. U., McCloskey, S. A., Postmastectomy radiation therapy after neoadjuvant chemotherapy: review and interpretation of available data, Ther Adv Med Oncol, 2016. 8(1): p. 85-97., https://www.ncbi.nlm.nih.gov/pubmed/26753007

846. Kantor, O., Pesce, C., Singh, P., Miller, M., Tseng, J., Wang, C. H., et.al. Post-mastectomy radiation therapy and overall survival after neoadjuvant chemotherapy, J Surg Oncol, 2017., https://www.ncbi.nlm.nih.gov/pubmed/28083910

847. Krug, D, Baumann, R, Budach, W, Dunst, J, Feyer, P, Fietkau, R, et.al. Individualization of post-mastectomy radiotherapy and regional nodal irradiation based on treatment response after neoadjuvant chemotherapy for breast cancer : A systematic review., Strahlenther Onkol, 2018. 194 (7)(7): p. 607-618., https://pubmed.ncbi.nlm.nih.gov/29383405/

848. Nikyar, N, Tegnelius, E, Valachis, A, Adjuvant locoregional radiation therapy in breast cancer patients with pathologic complete response after neoadjuvant chemotherapy: A systematic review and meta-analysis., Clin Transl Radiat Oncol, 2022. 33 (): p. 45-52., https://pubmed.ncbi.nlm.nih.gov/35036587/

849. Wang, K, Jin, X, Wang, W, Yu, X, Huang, J, The role of postmastectomy radiation in patients with ypN0 breast cancer after neoadjuvant chemotherapy: a meta-analysis., BMC Cancer, 2021. 21 (1)(1): p. 728., https://pubmed.ncbi.nlm.nih.gov/34172014/

850. de Wild, SR, de Munck, L, Simons, JM, Verloop, J, van Dalen, T, Elkhuizen, PHM, et.al. De-escalation of radiotherapy after primary chemotherapy in cT1-2N1 breast cancer (RAPCHEM; BOOG 2010-03): 5-year follow-up results of a Dutch, prospective, registry study., Lancet Oncol, 2022. 23 (9)(9): p. 1201-1210., https://pubmed.ncbi.nlm.nih.gov/35952707/

851. Krug, D, Baumann, R, Budach, W, Dunst, J, Feyer, P, Fietkau, R, et.al. Neoadjuvant chemotherapy for breast cancer-background for the indication of locoregional treatment., Strahlenther Onkol, 2018. 194 (9)(9): p. 797-805., https://pubmed.ncbi.nlm.nih.gov/29974132/

852. McGuire, S. E., Gonzalez-Angulo, A. M., Huang, E. H., Tucker, S. L., Kau, S. W., Yu, T. K., et.al. Postmastectomy radiation improves the outcome of patients with locally advanced breast cancer who achieve a pathologic complete response to neoadjuvant chemotherapy, Int J Radiat Oncol Biol Phys, 2007. 68(4): p. 1004-9., https://www.ncbi.nlm.nih.gov/pubmed/17418973

853. Nagar, H., Mittendorf, E. A., Strom, E. A., Perkins, G. H., Oh, J. L., Tereffe, W., et.al. Local-regional recurrence with and without radiation therapy after neoadjuvant chemotherapy and mastectomy for clinically staged T3N0 breast cancer, Int J Radiat Oncol Biol Phys, 2011. 81(3): p. 782-7., https://www.ncbi.nlm.nih.gov/pubmed/21885207

854. Nagar, H., Boothe, D., Ginter, P. S., Sison, C., Vahdat, L., Shin, S., et.al. Disease-free survival according to the use of postmastectomy radiation therapy after neoadjuvant chemotherapy, Clin Breast Cancer, 2015. 15(2): p. 128-34., https://www.ncbi.nlm.nih.gov/pubmed/25459070

855. Le Scodan, R., Selz, J., Stevens, D., Bollet, M. A., de la Lande, B., Daveau, C., et.al. Radiotherapy for stage II and stage III breast cancer patients with negative lymph nodes after preoperative chemotherapy and mastectomy, Int J Radiat Oncol Biol Phys, 2012. 82(1): p. e1-7., https://www.ncbi.nlm.nih.gov/pubmed/21377284

856. Shim, S. J., Park, W., Huh, S. J., Choi, D. H., Shin, K. H., Lee, N. K., et.al. The role of postmastectomy radiation therapy after neoadjuvant chemotherapy in clinical stage II-III breast cancer patients with pN0: a multicenter, retrospective study (KROG 12-05), Int J Radiat Oncol Biol Phys, 2014. 88(1): p. 65-72., https://www.ncbi.nlm.nih.gov/pubmed/24161425

857. Eleftherios Mamounas, Hanna Bandos, Julia White, Thomas Julian, Atif Khan, Simona Shaitelman, Mylin Torres, Frank Vicini, Patricia Ganz, Susan McCloskey, Nilendu Gupta, X. Allen Li, Peter Lucas, Nadeem Abu-Rustum, Saumil Gandhi, Rahul Tendulkar, Robert Coleman, Keiichi Fujiwara, Samantha Seaward, William Irvin, Kristin Higgins, Robert Mutter, Jean-Francois Boileau, Andrew Muskovitz, Reshma Jagsi, Anna Weiss, Curran Walter, Norman Wolmark, Abstract GS02-07: Loco-Regional Irradiation in Patients with Biopsy-proven Axillary Node Involvement at Presentation Who Become Pathologically Node-negative After Neoadjuvant Chemotherapy: Primary Outcomes of NRG Oncology/NSABP B-51/RTOG 1304ACR; Cancer Res 2024, 2023., https://doi.org/10.1158/1538-7445.sabcs23-gs02-07

858. Selz, J., Le Scodan, R., Menard, J., Hennequin, C., Quero, L., [Indication of radiotherapy after neoadjuvant chemotherapy in breast cancer], Cancer Radiother, 2014. 18(3): p. 229-34., https://www.ncbi.nlm.nih.gov/pubmed/24819247

859. Huang, E. H., Tucker, S. L., Strom, E. A., McNeese, M. D., Kuerer, H. M., Hortobagyi, G. N., et.al. Predictors of locoregional recurrence in patients with locally advanced breast cancer treated with neoadjuvant chemotherapy, mastectomy, and radiotherapy, Int J Radiat Oncol Biol Phys, 2005. 62(2): p. 351-7., https://www.ncbi.nlm.nih.gov/pubmed/15890574

860. Fowble, B. L., Einck, J. P., Kim, D. N., McCloskey, S., Mayadev, J., Yashar, C., et.al. Role of postmastectomy radiation after neoadjuvant chemotherapy in stage II-III breast cancer, Int J Radiat Oncol Biol Phys, 2012. 83(2): p. 494-503., https://www.ncbi.nlm.nih.gov/pubmed/22579377

861. Bernier, J., Post-mastectomy radiotherapy after neodjuvant chemotherapy in breast cancer patients: A review, Crit Rev Oncol Hematol, 2015. 93(3): p. 180-9., https://www.ncbi.nlm.nih.gov/pubmed/25465740

862. Rueth, N. M., Lin, H. Y., Bedrosian, I., Shaitelman, S. F., Ueno, N. T., Shen, Y., et.al. Underuse of trimodality treatment affects survival for patients with inflammatory breast cancer: an analysis of treatment and survival trends from the National Cancer Database, J Clin Oncol, 2014. 32(19): p. 2018-24., https://www.ncbi.nlm.nih.gov/pubmed/24888808

863. van Uden, D. J., Bretveld, R., Siesling, S., de Wilt, J. H., Blanken-Peeters, C. F., Inflammatory breast cancer in the Netherlands; improved survival over the last decades, Breast Cancer Res Treat, 2017. 162(2): p. 365-374., https://www.ncbi.nlm.nih.gov/pubmed/28138891

864. Hennequin, C., Bossard, N., Servagi-Vernat, S., Maingon, P., Dubois, J. B., Datchary, J., et.al. Ten-year survival results of a randomized trial of irradiation of internal mammary nodes after mastectomy, Int J Radiat Oncol Biol Phys, 2013. 86(5): p. 860-6., https://www.ncbi.nlm.nih.gov/pubmed/23664327

865. Budach, W., Bolke, E., Kammers, K., Gerber, P. A., Nestle-Kramling, C., Matuschek, C., Adjuvant radiation therapy of regional lymph nodes in breast cancer - a meta-analysis of randomized trials- an update, Radiat Oncol, 2015. 10: p. 258., https://www.ncbi.nlm.nih.gov/pubmed/26691175

866. Kim, YB, Byun, HK, Kim, DY, Ahn, SJ, Lee, HS, Park, W, et.al. Effect of Elective Internal Mammary Node Irradiation on Disease-Free Survival in Women With Node-Positive Breast Cancer: A Randomized Phase 3 Clinical Trial., JAMA Oncol, 2022. 8 (1)(1): p. 96-105., https://pubmed.ncbi.nlm.nih.gov/34695841/

867. Poortmans, PM, Weltens, C, Fortpied, C, Kirkove, C, Peignaux-Casasnovas, K, Budach, V, et.al. Internal mammary and medial supraclavicular lymph node chain irradiation in stage I-III breast cancer (EORTC 22922/10925): 15-year results of a randomised, phase 3 trial., Lancet Oncol, 2020. 21 (12)(12): p. 1602-1610., https://pubmed.ncbi.nlm.nih.gov/33152277/

868. Thorsen, LBJ, Overgaard, J, Matthiessen, LW, Berg, M, Stenbygaard, L, Pedersen, AN, et.al. Internal Mammary Node Irradiation in Patients With Node-Positive Early Breast Cancer: Fifteen-Year Results From the Danish Breast Cancer Group Internal Mammary Node Study., J Clin Oncol, 2022. 40 (36)(36): p. 4198-4206., https://pubmed.ncbi.nlm.nih.gov/35394824/

869. Recht, A., Edge, S. B., Solin, L. J., Robinson, D. S., Estabrook, A., Fine, R. E., et.al. Postmastectomy radiotherapy: clinical practice guidelines of the American Society of Clinical Oncology, J Clin Oncol, 2001. 19(5): p. 1539-69., https://www.ncbi.nlm.nih.gov/pubmed/11230499

870. Yates, L., Kirby, A., Crichton, S., Gillett, C., Cane, P., Fentiman, I., et.al. Risk factors for regional nodal relapse in breast cancer patients with one to three positive axillary nodes, Int J Radiat Oncol Biol Phys, 2012. 82(5): p. 2093-103., https://www.ncbi.nlm.nih.gov/pubmed/21530101

871. Poortmans, Philip M, Collette, Sandra, Kirkove, Carine, Van Limbergen, Erik, Budach, Volker, Struikmans, Henk, et.al. Internal mammary and medial supraclavicular irradiation in breast cancer, New England Journal of Medicine, 2015. 373(4): p. 317-327., https://www.ncbi.nlm.nih.gov/pubmed/26200978

872. Thorsen, L. B., Offersen, B. V., Dano, H., Berg, M., Jensen, I., Pedersen, A. N., et.al. DBCG-IMN: A Population-Based Cohort Study on the Effect of Internal Mammary Node Irradiation in Early Node-Positive Breast Cancer, J Clin Oncol, 2016. 34(4): p. 314-20., https://www.ncbi.nlm.nih.gov/pubmed/26598752

873. Whelan, Timothy J, Olivotto, Ivo A, Parulekar, Wendy R, Ackerman, Ida, Chua, Boon H, Nabid, Abdenour, et.al. Regional nodal irradiation in early-stage breast cancer, New England Journal of Medicine, 2015. 373(4): p. 307-316., https://pubmed.ncbi.nlm.nih.gov/26200977/

874. Hennequin, C., Bossard, N., Servagi-Vernat, S., Maingon, P., Dubois, J. B., Datchary, J., et.al. Ten-year survival results of a randomized trial of irradiation of internal mammary nodes after mastectomy, Int J Radiat Oncol Biol Phys, 2013. 86(5): p. 860-6., https://www.ncbi.nlm.nih.gov/pubmed/23664327

875. Budach, W., Bolke, E., Kammers, K., Gerber, P. A., Nestle-Kramling, C., Matuschek, C., Adjuvant radiation therapy of regional lymph nodes in breast cancer - a meta-analysis of randomized trials- an update, Radiat Oncol, 2015. 10: p. 258., https://www.ncbi.nlm.nih.gov/pubmed/26691175

876. Korzets, Yasmin, Levitas, Dina, Grubstein, Ahuva, Corn, Benjamin, Amir, Eitan, Goldvaser, Hadar, Efficacy and Safety of the Addition of Internal Mammary Irradiation to Standard Adjuvant Radiation in Early-Stage Breast Cancer: A Systematic Review and Meta-Analysis, 2022/09/17. 29: p. 6657 - 6673., https://pubmed.ncbi.nlm.nih.gov/36135092/

877. Jia, Sicong, Liu, Zhikun, Zhang, Jun, Zhao, Chenguang, Zhu, Longyu, Kong, Jie, et.al. Can internal mammary lymph nodes irradiation bring survival benefits for breast cancer patients? A systematic review and meta-analysis of 12,705 patients in 12 studies, 2021/02/23. 16:, https://pubmed.ncbi.nlm.nih.gov/33622345/

878. Caussa, L., Kirova, Y. M., Gault, N., Pierga, J. Y., Savignoni, A., Campana, F., et.al. The acute skin and heart toxicity of a concurrent association of trastuzumab and locoregional breast radiotherapy including internal mammary chain: a single-institution study, Eur J Cancer, 2011. 47(1): p. 65-73., https://www.ncbi.nlm.nih.gov/pubmed/20843680

879. Shaffer, R., Tyldesley, S., Rolles, M., Chia, S., Mohamed, I., Acute cardiotoxicity with concurrent trastuzumab and radiotherapy including internal mammary chain nodes: a retrospective single-institution study, Radiother Oncol, 2009. 90(1): p. 122-6., https://www.ncbi.nlm.nih.gov/pubmed/18976826

880. Thorsen, L. B., Thomsen, M. S., Berg, M., Jensen, I., Josipovic, M., Overgaard, M., et.al. CT-planned internal mammary node radiotherapy in the DBCG-IMN study: benefit versus potentially harmful effects, Acta Oncol, 2014. 53(8): p. 1027-34., https://www.ncbi.nlm.nih.gov/pubmed/24957557

881. Popescu, C. C., Olivotto, I. A., Beckham, W. A., Ansbacher, W., Zavgorodni, S., Shaffer, R., et.al. Volumetric modulated arc therapy improves dosimetry and reduces treatment time compared to conventional intensity-modulated radiotherapy for locoregional radiotherapy of left-sided breast cancer and internal mammary nodes, Int J Radiat Oncol Biol Phys, 2010. 76(1): p. 287-95., https://www.ncbi.nlm.nih.gov/pubmed/19775832

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897. Bartelink, H., Rubens, R. D., van der Schueren, E., Sylvester, R., Hormonal therapy prolongs survival in irradiated locally advanced breast cancer: a European Organization for Research and Treatment of Cancer Randomized Phase III Trial, J Clin Oncol, 1997. 15(1): p. 207-15., https://www.ncbi.nlm.nih.gov/pubmed/8996144

898. Scotti, V., Desideri, I., Meattini, I., Di Cataldo, V., Cecchini, S., Petrucci, A., et.al. Management of inflammatory breast cancer: focus on radiotherapy with an evidence-based approach, Cancer Treat Rev, 2013. 39(2): p. 119-24., https://www.ncbi.nlm.nih.gov/pubmed/22564719

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900. Gaui, MF, Amorim, G, Arcuri, RA, Pereira, G, Moreira, D, Djahjah, C, et.al. A phase II study of second-line neoadjuvant chemotherapy with capecitabine and radiation therapy for anthracycline-resistant locally advanced breast cancer., Am J Clin Oncol, 2007. 30 (1)(1): p. 78-81., https://pubmed.ncbi.nlm.nih.gov/17278899/

901. Woodward, WA, Fang, P, Arriaga, L, Gao, H, Cohen, EN, Reuben, JM, et.al. A phase 2 study of capecitabine and concomitant radiation in women with advanced breast cancer., Int J Radiat Oncol Biol Phys, 2017. 99 (4)(4): p. 777-783., https://pubmed.ncbi.nlm.nih.gov/28843370/

902. Jagsi, R, Mason, G, Overmoyer, BA, Woodward, WA, Badve, S, Schneider, RJ, et.al. Inflammatory breast cancer defined: proposed common diagnostic criteria to guide treatment and research., Breast Cancer Res Treat, 2022. 192 (2)(2): p. 235-243., https://pubmed.ncbi.nlm.nih.gov/34973083/

903. McGuire, S. E., Gonzalez-Angulo, A. M., Huang, E. H., Tucker, S. L., Kau, S. W., Yu, T. K., et.al. Postmastectomy radiation improves the outcome of patients with locally advanced breast cancer who achieve a pathologic complete response to neoadjuvant chemotherapy, Int J Radiat Oncol Biol Phys, 2007. 68(4): p. 1004-9., https://www.ncbi.nlm.nih.gov/pubmed/17418973

904. Nagar, H., Mittendorf, E. A., Strom, E. A., Perkins, G. H., Oh, J. L., Tereffe, W., et.al. Local-regional recurrence with and without radiation therapy after neoadjuvant chemotherapy and mastectomy for clinically staged T3N0 breast cancer, Int J Radiat Oncol Biol Phys, 2011. 81(3): p. 782-7., https://www.ncbi.nlm.nih.gov/pubmed/21885207

905. Nagar, H., Boothe, D., Ginter, P. S., Sison, C., Vahdat, L., Shin, S., et.al. Disease-free survival according to the use of postmastectomy radiation therapy after neoadjuvant chemotherapy, Clin Breast Cancer, 2015. 15(2): p. 128-34., https://www.ncbi.nlm.nih.gov/pubmed/25459070

906. Ahmed, M, Jozsa, F, Douek, M, A systematic review of neo-adjuvant radiotherapy in the treatment of breast cancer., Ecancermedicalscience, 2021. 15 (): p. 1175., https://pubmed.ncbi.nlm.nih.gov/33680089/

907. Corradini, S, Krug, D, Meattini, I, Matuschek, C, Bölke, E, Francolini, G, et.al. Preoperative radiotherapy: A paradigm shift in the treatment of breast cancer? A review of literature., Crit Rev Oncol Hematol, 2019. 141 (): p. 102-111., https://pubmed.ncbi.nlm.nih.gov/31272045/

908. Bellon, J. R., Come, S. E., Gelman, R. S., Henderson, I. C., Shulman, L. N., Silver, B. J., et.al. Sequencing of chemotherapy and radiation therapy in early-stage breast cancer: updated results of a prospective randomized trial, J Clin Oncol, 2005. 23(9): p. 1934-40., https://www.ncbi.nlm.nih.gov/pubmed/15774786

909. Hickey, B. E., Francis, D., Lehman, M. H., Sequencing of chemotherapy and radiation therapy for early breast cancer, Cochrane Database Syst Rev, 2006. p. Cd005212., https://www.ncbi.nlm.nih.gov/pubmed/23633328

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911. Pinnaro, P., Rambone, R., Giordano, C., Giannarelli, D., Strigari, L., Arcangeli, G., Long-term results of a randomized trial on the sequencing of radiotherapy and chemotherapy in breast cancer, Am J Clin Oncol, 2011. 34(3): p. 238-44., https://www.ncbi.nlm.nih.gov/pubmed/20805741

912. Chen, Z., King, W., Pearcey, R., Kerba, M., Mackillop, W. J., The relationship between waiting time for radiotherapy and clinical outcomes: a systematic review of the literature, Radiother Oncol, 2008. 87(1): p. 3-16., https://www.ncbi.nlm.nih.gov/pubmed/18160158

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914. Li, Y. F., Chang, L., Li, W. H., Xiao, M. Y., Wang, Y., He, W. J., et.al. Radiotherapy concurrent versus sequential with endocrine therapy in breast cancer: A meta-analysis, Breast, 2016. 27: p. 93-8., https://www.ncbi.nlm.nih.gov/pubmed/27054754

915. Tsoutsou, PG, Belkacemi, Y, Gligorov, J, Kuten, A, Boussen, H, Bese, N, et.al. Optimal sequence of implied modalities in the adjuvant setting of breast cancer treatment: an update on issues to consider., Oncologist, 2010. 15 (11)(11): p. 1169-78., https://pubmed.ncbi.nlm.nih.gov/21041378/

916. Karlsson, P, Cole, BF, Colleoni, M, Roncadin, M, Chua, BH, Murray, E, et.al. Timing of radiotherapy and outcome in patients receiving adjuvant endocrine therapy., Int J Radiat Oncol Biol Phys, 2011. 80 (2)(2): p. 398-402., https://pubmed.ncbi.nlm.nih.gov/20729007/

917. Winzer, KJ, Sauerbrei, W, Braun, M, Liersch, T, Dunst, J, Guski, H, et.al. Radiation therapy and tamoxifen after breast-conserving surgery: updated results of a 2 x 2 randomised clinical trial in patients with low risk of recurrence., Eur J Cancer, 2010. 46 (1)(1): p. 95-101., https://pubmed.ncbi.nlm.nih.gov/19879131/

918. Azria, D, Belkacemi, Y, Romieu, G, Gourgou, S, Gutowski, M, Zaman, K, et.al. Concurrent or sequential adjuvant letrozole and radiotherapy after conservative surgery for early-stage breast cancer (CO-HO-RT): a phase 2 randomised trial., Lancet Oncol, 2010. 11 (3)(3): p. 258-65., https://pubmed.ncbi.nlm.nih.gov/20138810/

919. Bourgier, C, Kerns, S, Gourgou, S, Lemanski, C, Gutowski, M, Fenoglietto, P, et.al. Concurrent or sequential letrozole with adjuvant breast radiotherapy: final results of the CO-HO-RT phase II randomized trial., Ann Oncol, 2016. 27 (3)(3): p. 474-80., https://pubmed.ncbi.nlm.nih.gov/26681684/

920. Meattini, I, Becherini, C, Caini, S, Coles, CE, Cortes, J, Curigliano, G, et.al. International multidisciplinary consensus on the integration of radiotherapy with new systemic treatments for breast cancer: European Society for Radiotherapy and Oncology (ESTRO)-endorsed recommendations., Lancet Oncol, 2024. 25 (2)(2): p. e73-e83., https://pubmed.ncbi.nlm.nih.gov/38301705/

921. Matuschek, Christiane, Bölke, Edwin, Haussmann, Jan, Mohrmann, Svjetlana, Nestle-Krämling, Carolin, Gerber, Peter Arne, et.al. The benefit of adjuvant radiotherapy after breast conserving surgery in older patients with low risk breast cancer- a meta-analysis of randomized trials, 2017. 12(1): p. 60., https://doi.org/10.1186/s13014-017-0796-x

922. McGee, S.F., Mazzarello, Sasha, Caudrelier, Jean-Michel, Lima, M.A.G., Hutton, Brian, Sienkiewicz, M., et.al. Optimal Sequence of Adjuvant Endocrine and Radiation Therapy in Early-Stage Breast Cancer – A Systematic Review, 2018/06/01. 69:, https://pubmed.ncbi.nlm.nih.gov/30014951/

923. Bachir, B, Anouti, S, Abi Jaoude, J, Kayali, M, Tfayli, A, de Azambuja, E, et.al. Evaluation of Cardiotoxicity in HER-2-Positive Breast Cancer Patients Treated With Radiation Therapy and Trastuzumab., Int J Radiat Oncol Biol Phys, 2022. 113 (1)(1): p. 135-142., https://pubmed.ncbi.nlm.nih.gov/34986381/

924. Belkacémi, Y, Gligorov, J, Concurrent trastuzumab--internal mammary irradiation for HER2 positive breast cancer: "It hurts to be on the cutting edge"., Radiother Oncol, 2010. 94 (1)(1): p. 119-20; author reply 120-1., https://pubmed.ncbi.nlm.nih.gov/19410315/

925. Belkacémi, Y, Gligorov, J, Ozsahin, M, Marsiglia, H, De Lafontan, B, Laharie-Mineur, H, et.al. Concurrent trastuzumab with adjuvant radiotherapy in HER2-positive breast cancer patients: acute toxicity analyses from the French multicentric study., Ann Oncol, 2008. 19 (6)(6): p. 1110-6., https://pubmed.ncbi.nlm.nih.gov/18344537/

926. Jacob, J, Belin, L, Pierga, JY, Gobillion, A, Vincent-Salomon, A, Dendale, R, et.al. Concurrent administration of trastuzumab with locoregional breast radiotherapy: long-term results of a prospective study., Breast Cancer Res Treat, 2014. 148 (2)(2): p. 345-53., https://pubmed.ncbi.nlm.nih.gov/25318926/

927. Caussa, L, Kirova, YM, Gault, N, Pierga, JY, Savignoni, A, Campana, F, et.al. The acute skin and heart toxicity of a concurrent association of trastuzumab and locoregional breast radiotherapy including internal mammary chain: a single-institution study., Eur J Cancer, 2011. 47 (1)(1): p. 65-73., https://pubmed.ncbi.nlm.nih.gov/20843680/

928. Aboudaram, A, Loap, P, Loirat, D, Dhia, SB, Cao, K, Fourquet, A, et.al. Pertuzumab and Trastuzumab Combination with Concomitant Locoregional Radiotherapy for the Treatment of Breast Cancers with HER2 Receptor Overexpression., Cancers (Basel), 2021. 13 (19)(19):, https://pubmed.ncbi.nlm.nih.gov/34638275/

929. de Azambuja, E, Agostinetto, E, Procter, M, Eiger, D, Pondé, N, Guillaume, S, et.al. Cardiac safety of dual anti-HER2 blockade with pertuzumab plus trastuzumab in early HER2-positive breast cancer in the APHINITY trial., ESMO Open, 2023. 8 (1)(1): p. 100772., https://pubmed.ncbi.nlm.nih.gov/36681013/

930. von Minckwitz, G, Procter, M, de Azambuja, E, Zardavas, D, Benyunes, M, Viale, G, et.al. Adjuvant Pertuzumab and Trastuzumab in Early HER2-Positive Breast Cancer., N Engl J Med, 2017. 377 (2)(2): p. 122-131., https://pubmed.ncbi.nlm.nih.gov/28581356/

931. von Minckwitz, G, Huang, CS, Mano, MS, Loibl, S, Mamounas, EP, Untch, M, et.al. Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer., N Engl J Med, 2019. 380 (7)(7): p. 617-628., https://pubmed.ncbi.nlm.nih.gov/30516102/

932. Bellon, JR, Tayob, N, Yang, DD, Tralins, J, Dang, CT, Isakoff, SJ, et.al. Local Therapy Outcomes and Toxicity From the ATEMPT Trial (TBCRC 033): A Phase II Randomized Trial of Adjuvant Trastuzumab Emtansine Versus Paclitaxel in Combination With Trastuzumab in Women With Stage I HER2-Positive Breast Cancer., Int J Radiat Oncol Biol Phys, 2022. 113 (1)(1): p. 117-124., https://pubmed.ncbi.nlm.nih.gov/34990776/

933. Salvestrini, V, Kim, K, Caini, S, Alkner, S, Ekholm, M, Skyttä, T, et.al. Safety profile of trastuzumab-emtansine (T-DM1) with concurrent radiation therapy: A systematic review and meta-analysis., Radiother Oncol, 2023. 186 (): p. 109805., https://pubmed.ncbi.nlm.nih.gov/37437610/

934. Piroth, MD, Krug, D, Sedlmayer, F, Duma, MN, Baumann, R, Budach, W, et.al. Post-neoadjuvant treatment with capecitabine and trastuzumab emtansine in breast cancer patients-sequentially, or better simultaneously?, Strahlenther Onkol, 2021. 197 (1)(1): p. 1-7., https://pubmed.ncbi.nlm.nih.gov/32737515/

935. McArthur, Heather, Cortes, Javier, Dent, Rebecca, O’Shaughnessy, Joyce, Pusztai, Lajos, Küemmel, Sherko, et.al. Abstract PD3-01: Neoadjuvant pembrolizumab + chemotherapy vs placebo + chemotherapy followed by adjuvant pembrolizumab vs placebo for early TNBC: Post hoc analysis of adjuvant radiation therapy in the phase 3 KEYNOTE-522 study, 2023/03/01. 83: p. PD3 - 01.

936. Schmid, P, Cortes, J, Dent, R, Pusztai, L, McArthur, H, Kümmel, S, et.al. Event-free Survival with Pembrolizumab in Early Triple-Negative Breast Cancer., N Engl J Med, 2022. 386 (6)(6): p. 556-567., https://pubmed.ncbi.nlm.nih.gov/35139274/

937. Becherini, C, Visani, L, Caini, S, Bhattacharya, IS, Kirby, AM, Nader Marta, G, et.al. Safety profile of cyclin-dependent kinase (CDK) 4/6 inhibitors with concurrent radiation therapy: A systematic review and meta-analysis., Cancer Treat Rev, 2023. 119 (): p. 102586., https://pubmed.ncbi.nlm.nih.gov/37336117/

938. Balduzzi, A., Leonardi, M. C., Cardillo, A., Orecchia, R., Dellapasqua, S., Iorfida, M., et.al. Timing of adjuvant systemic therapy and radiotherapy after breast-conserving surgery and mastectomy, Cancer Treat Rev, 2010. 36(6): p. 443-50., https://www.ncbi.nlm.nih.gov/pubmed/20304562

939. Benchalal, M., Le Prise, E., de Lafontan, B., Berton-Rigaud, D., Belkacemi, Y., Romestaing, P., et.al. Influence of the time between surgery and radiotherapy on local recurrence in patients with lymph node-positive, early-stage, invasive breast carcinoma undergoing breast-conserving surgery: results of the French Adjuvant Study Group, Cancer, 2005. 104(2): p. 240-50., https://www.ncbi.nlm.nih.gov/pubmed/15948160

940. Azria, D., Belkacemi, Y., Romieu, G., Gourgou, S., Gutowski, M., Zaman, K., et.al. Concurrent or sequential adjuvant letrozole and radiotherapy after conservative surgery for early-stage breast cancer (CO-HO-RT): a phase 2 randomised trial, Lancet Oncol, 2010. 11(3): p. 258-65., https://www.ncbi.nlm.nih.gov/pubmed/20138810

941. Bourgier, C., Kerns, S., Gourgou, S., Lemanski, C., Gutowski, M., Fenoglietto, P., et.al. Concurrent or sequential letrozole with adjuvant breast radiotherapy: final results of the CO-HO-RT phase II randomized trial, Ann Oncol, 2016. 27(3): p. 474-80., https://www.ncbi.nlm.nih.gov/pubmed/26681684

942. Ishitobi, M., Komoike, Y., Motomura, K., Koyama, H., Nishiyama, K., Inaji, H., Retrospective analysis of concurrent vs. sequential administration of radiotherapy and hormone therapy using aromatase inhibitor for hormone receptor-positive postmenopausal breast cancer, Anticancer Res, 2009. 29(11): p. 4791-4., https://www.ncbi.nlm.nih.gov/pubmed/20032437

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945. Tsoutsou, P. G., Belkacemi, Y., Gligorov, J., Kuten, A., Boussen, H., Bese, N., et.al. Optimal sequence of implied modalities in the adjuvant setting of breast cancer treatment: an update on issues to consider, Oncologist, 2010. 15(11): p. 1169-78., https://www.ncbi.nlm.nih.gov/pubmed/21041378

946. Schmid, P, Cortes, J, Pusztai, L, McArthur, H, Kümmel, S, Bergh, J, et.al. Pembrolizumab for Early Triple-Negative Breast Cancer., N Engl J Med, 2020. 382 (9)(9): p. 810-821., https://pubmed.ncbi.nlm.nih.gov/32101663/

947. Gnant, M, Dueck, AC, Frantal, S, Martin, M, Burstein, HJ, Greil, R, et.al. Adjuvant Palbociclib for Early Breast Cancer: The PALLAS Trial Results (ABCSG-42/AFT-05/BIG-14-03)., J Clin Oncol, 2022. 40 (3)(3): p. 282-293., https://pubmed.ncbi.nlm.nih.gov/34874182/

948. Loibl, S, Marmé, F, Martin, M, Untch, M, Bonnefoi, H, Kim, SB, et.al. Palbociclib for Residual High-Risk Invasive HR-Positive and HER2-Negative Early Breast Cancer-The Penelope-B Trial., J Clin Oncol, 2021. 39 (14)(14): p. 1518-1530., https://pubmed.ncbi.nlm.nih.gov/33793299/

949. Loap, P, Loirat, D, Berger, F, Rodrigues, M, Bazire, L, Pierga, JY, et.al. Concurrent Olaparib and Radiotherapy in Patients With Triple-Negative Breast Cancer: The Phase 1 Olaparib and Radiation Therapy for Triple-Negative Breast Cancer Trial., JAMA Oncol, 2022. 8 (12)(12): p. 1802-1808., https://pubmed.ncbi.nlm.nih.gov/36301572/

950. Jagsi, R, Griffith, KA, Bellon, JR, Woodward, WA, Horton, JK, Ho, A, et.al. Concurrent Veliparib With Chest Wall and Nodal Radiotherapy in Patients With Inflammatory or Locoregionally Recurrent Breast Cancer: The TBCRC 024 Phase I Multicenter Study., J Clin Oncol, 2018. 36 (13)(13): p. 1317-1322., https://pubmed.ncbi.nlm.nih.gov/29558281/

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957. Campbell, KL, Winters-Stone, KM, Wiskemann, J, May, AM, Schwartz, AL, Courneya, KS, et.al. Exercise Guidelines for Cancer Survivors: Consensus Statement from International Multidisciplinary Roundtable., Med Sci Sports Exerc, 2019. 51 (11)(11): p. 2375-2390., https://pubmed.ncbi.nlm.nih.gov/31626055/

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996. Wang, K, Li, F, Zhang, X, Li, Z, Li, H, Smoking increases risks of all-cause and breast cancer specific mortality in breast cancer individuals: a dose-response meta-analysis of prospective cohort studies involving 39725 breast cancer cases., Oncotarget, 2016. 7 (50)(50): p. 83134-83147., https://pubmed.ncbi.nlm.nih.gov/27863414/

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999. Kwan, ML, Kushi, LH, Weltzien, E, Tam, EK, Castillo, A, Sweeney, C, et.al. Alcohol consumption and breast cancer recurrence and survival among women with early-stage breast cancer: the life after cancer epidemiology study., J Clin Oncol, 2010. 28 (29)(29): p. 4410-6., https://pubmed.ncbi.nlm.nih.gov/20805458/

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1017. Gnant, M, Fitzal, F, Rinnerthaler, G, Steger, GG, Greil-Ressler, S, Balic, M, et.al. Duration of Adjuvant Aromatase-Inhibitor Therapy in Postmenopausal Breast Cancer., N Engl J Med, 2021. 385 (5)(5): p. 395-405., https://pubmed.ncbi.nlm.nih.gov/34320285/

1018. Blok, EJ, Kroep, JR, Meershoek-Klein Kranenbarg, E, Duijm-de Carpentier, M, Putter, H, van den Bosch, J, et.al. Optimal Duration of Extended Adjuvant Endocrine Therapy for Early Breast Cancer; Results of the IDEAL Trial (BOOG 2006-05)., J Natl Cancer Inst, 2018. 110 (1)(1):, https://pubmed.ncbi.nlm.nih.gov/28922787/

1019. Aromatase inhibitors versus tamoxifen in premenopausal women with oestrogen receptor-positive early-stage breast cancer treated with ovarian suppression: a patient-level meta-analysis of 7030 women from four randomised trials., Lancet Oncol, 2022. 23 (3)(3): p. 382-392., https://pubmed.ncbi.nlm.nih.gov/35123662/

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1683. Simon, P, Barrou, J, Cohen, M, Rua, S, Lambaudie, E, Houvenaeghel, G, Types of Mastectomies and Immediate Reconstructions for Ipsilateral Breast Local Recurrences., Front Oncol, 2020. 10 (): p. 567298., https://pubmed.ncbi.nlm.nih.gov/33363007/

1684. Delenne, S, Philip, CA, Guimont, I, Bienstman, J, Mojallal, AA, Cortet, M, Mastectomies for breast cancer: Comparison between peri-operative morbidity after simple mastectomy or after immediate breast reconstruction in a unicentric serie of 210 patients., J Gynecol Obstet Hum Reprod, 2024. 53 (1)(1): p. 102695., https://pubmed.ncbi.nlm.nih.gov/37995939/

1685. Browne, JP, Jeevan, R, Gulliver-Clarke, C, Pereira, J, Caddy, CM, van der Meulen, JHP, The association between complications and quality of life after mastectomy and breast reconstruction for breast cancer., Cancer, 2017. 123 (18)(18): p. 3460-3467., https://pubmed.ncbi.nlm.nih.gov/28513834/

1686. Eriksen, C, Frisell, J, Wickman, M, Lidbrink, E, Krawiec, K, Sandelin, K, Immediate reconstruction with implants in women with invasive breast cancer does not affect oncological safety in a matched cohort study., Breast Cancer Res Treat, 2011. 127 (2)(2): p. 439-46., https://pubmed.ncbi.nlm.nih.gov/21409394/

1687. Ryu, JM, Paik, HJ, Park, S, Yi, HW, Nam, SJ, Kim, SW, et.al. Oncologic Outcomes after Immediate Breast Reconstruction Following Total Mastectomy in Patients with Breast Cancer: A Matched Case-Control Study., J Breast Cancer, 2017. 20 (1)(1): p. 74-81., https://pubmed.ncbi.nlm.nih.gov/28382097/

1688. O'Connell, RL, Rattay, T, Dave, RV, Trickey, A, Skillman, J, Barnes, NLP, et.al. The impact of immediate breast reconstruction on the time to delivery of adjuvant therapy: the iBRA-2 study., Br J Cancer, 2019. 120 (9)(9): p. 883-895., https://pubmed.ncbi.nlm.nih.gov/30923359/

1689. Lagendijk, M, van Egdom, LSE, van Veen, FEE, Vos, EL, Mureau, MAM, van Leeuwen, N, et.al. Patient-Reported Outcome Measures May Add Value in Breast Cancer Surgery., Ann Surg Oncol, 2018. 25 (12)(12): p. 3563-3571., https://pubmed.ncbi.nlm.nih.gov/30178391/

1690. Roy, N, Downes, MH, Ibelli, T, Amakiri, UO, Li, T, Tebha, SS, et.al. The psychological impacts of post-mastectomy breast reconstruction: a systematic review., Ann Breast Surg, 2024. 8 ():, https://pubmed.ncbi.nlm.nih.gov/39100730/

1691. Yoon, AP, Qi, J, Brown, DL, Kim, HM, Hamill, JB, Erdmann-Sager, J, et.al. Outcomes of immediate versus delayed breast reconstruction: Results of a multicenter prospective study., Breast, 2018. 37 (): p. 72-79., https://pubmed.ncbi.nlm.nih.gov/29102781/

1692. Broyles, JM, Balk, EM, Adam, GP, Cao, W, Bhuma, MR, Mehta, S, et.al. Implant-based versus Autologous Reconstruction after Mastectomy for Breast Cancer: A Systematic Review and Meta-analysis., Plast Reconstr Surg Glob Open, 2022. 10 (3)(3): p. e4180., https://pubmed.ncbi.nlm.nih.gov/35291333/

1693. Miseré, RM, van Kuijk, SM, Claassens, EL, Heuts, EM, Piatkowski, AA, van der Hulst, RR, Breast-related and body-related quality of life following autologous breast reconstruction is superior to implant-based breast reconstruction - A long-term follow-up study., Breast, 2021. 59 (): p. 176-182., https://pubmed.ncbi.nlm.nih.gov/34271290/

1694. Persichetti, P, Barone, M, Salzillo, R, Cogliandro, A, Brunetti, B, Ciarrocchi, S, et.al. Impact on Patient's Appearance Perception of Autologous and Implant Based Breast Reconstruction Following Mastectomy Using BREAST-Q., Aesthetic Plast Surg, 2022. 46 (3)(3): p. 1153-1163., https://pubmed.ncbi.nlm.nih.gov/35229192/

1695. Sadok, N, Krabbe-Timmerman, IS, Buisman, NH, van Aalst, VC, de Bock, GH, Werker, PMN, Short-Term Quality of Life after Autologous Compared with Alloplastic Breast Reconstruction: A Prospective Study., Plast Reconstr Surg, 2023. 152 (4S)(4S): p. 55S-68S., https://pubmed.ncbi.nlm.nih.gov/37036311/

1696. von Glinski, M, Holler, N, Kümmel, S, Reinisch, M, Wallner, C, Wagner, JM, et.al. Autologous vs. implant-based breast reconstruction after skin- and nipple-sparing mastectomy-A deeper insight considering surgical and patient-reported outcomes., Front Surg, 2022. 9 (): p. 903734., https://pubmed.ncbi.nlm.nih.gov/36132203/

1697. Cai, L, Momeni, A, The Impact of Reconstructive Modality and Postoperative Complications on Decision Regret and Patient-Reported Outcomes following Breast Reconstruction., Aesthetic Plast Surg, 2022. 46 (2)(2): p. 655-660., https://pubmed.ncbi.nlm.nih.gov/34845512/

1698. Gao, P, Bai, P, Kong, X, Fang, Y, Gao, J, Wang, J, Patient-Reported Outcomes and Complications Following Breast Reconstruction: A Comparison Between Biological Matrix-Assisted Direct-to-Implant and Latissimus Dorsi Flap., Front Oncol, 2022. 12 (): p. 766076., https://pubmed.ncbi.nlm.nih.gov/35155227/

1699. Nelson, JA, Shamsunder, MG, Myers, PL, Polanco, TO, Coriddi, MR, McCarthy, CM, et.al. Matched Preliminary Analysis of Patient-Reported Outcomes following Autologous and Implant-Based Breast Reconstruction., Ann Surg Oncol, 2022. 29 (8)(8): p. 5266-5275., https://pubmed.ncbi.nlm.nih.gov/35366702/

1700. Eltahir, Y, Werners, LLCH, Dreise, MM, Zeijlmans van Emmichoven, IA, Werker, PMN, de Bock, GH, Which breast is the best? Successful autologous or alloplastic breast reconstruction: patient-reported quality-of-life outcomes., Plast Reconstr Surg, 2015. 135 (1)(1): p. 43-50., https://pubmed.ncbi.nlm.nih.gov/25539295/

1701. Kouwenberg, CAE, de Ligt, KM, Kranenburg, LW, Rakhorst, H, de Leeuw, D, Siesling, S, et.al. Long-Term Health-Related Quality of Life after Four Common Surgical Treatment Options for Breast Cancer and the Effect of Complications: A Retrospective Patient-Reported Survey among 1871 Patients., Plast Reconstr Surg, 2020. 146 (1)(1): p. 1-13., https://pubmed.ncbi.nlm.nih.gov/32590633/

1702. McCarthy, CM, Mehrara, BJ, Long, T, Garcia, P, Kropf, N, Klassen, AF, et.al. Chest and upper body morbidity following immediate postmastectomy breast reconstruction., Ann Surg Oncol, 2014. 21 (1)(1): p. 107-12., https://pubmed.ncbi.nlm.nih.gov/24201740/

1703. Brito, Íris M., Fernandes, Andreia, Andresen, Carolina, Barbosa, Rui, Ribeiro, Matilde, Valença-Filipe, Rita, Patient satisfaction with breast reconstruction: how much do timing and surgical technique matter?, 2020. 43(6): p. 809 - 818., https://doi.org/10.1007/s00238-020-01663-7

1704. Tallroth, L, Velander, P, Klasson, S, A short-term comparison of expander prosthesis and DIEP flap in breast reconstructions: A prospective randomized study., J Plast Reconstr Aesthet Surg, 2021. 74 (6)(6): p. 1193-1202., https://pubmed.ncbi.nlm.nih.gov/33436336/

1705. Bachour, Y, Bargon, CA, de Blok, CJM, Ket, JCF, Ritt, MJPF, Niessen, FB, Risk factors for developing capsular contracture in women after breast implant surgery: A systematic review of the literature., J Plast Reconstr Aesthet Surg, 2018. 71 (9)(9): p. e29-e48., https://pubmed.ncbi.nlm.nih.gov/29980456/

1706. Hillard, C, Fowler, JD, Barta, R, Cunningham, B, Silicone breast implant rupture: a review., Gland Surg, 2017. 6 (2)(2): p. 163-168., https://pubmed.ncbi.nlm.nih.gov/28497020/

1707. McGuire, P, Clauw, DJ, Hammer, J, Haws, M, Adams, WP, A Practical Guide to Managing Patients With Systemic Symptoms and Breast Implants., Aesthet Surg J, 2022. 42 (4)(4): p. 397-407., https://pubmed.ncbi.nlm.nih.gov/34687293/

1708. Niraula, S, Katel, A, Barua, A, Weiss, A, Strawderman, MS, Zhang, H, et.al. A Systematic Review of Breast Implant-Associated Squamous Cell Carcinoma., Cancers (Basel), 2023. 15 (18)(18):, https://pubmed.ncbi.nlm.nih.gov/37760485/

1709. Santanelli di Pompeo, F, Clemens, MW, Atlan, M, Botti, G, Cordeiro, PG, De Jong, D, et.al. 2022 Practice Recommendation Updates From the World Consensus Conference on BIA-ALCL., Aesthet Surg J, 2022. 42 (11)(11): p. 1262-1278., https://pubmed.ncbi.nlm.nih.gov/35639805/

1710. Santanelli di Pompeo, F, Clemens, MW, Paolini, G, Firmani, G, Panagiotakos, D, Sorotos, M, Epidemiology of Breast Implant-Associated Anaplastic Large Cell Lymphoma in the United States: A Systematic Review., Aesthet Surg J, 2023. 44 (1)(1): p. NP32-NP40., https://pubmed.ncbi.nlm.nih.gov/37616552/

1711. McCarthy, CM, Loyo-Berríos, N, Qureshi, AA, Mullen, E, Gordillo, G, Pusic, AL, et.al. Patient Registry and Outcomes for Breast Implants and Anaplastic Large Cell Lymphoma Etiology and Epidemiology (PROFILE): Initial Report of Findings, 2012-2018., Plast Reconstr Surg, 2019. 143 (3S A Review of Breast Implant-Associated Anaplastic Large Cell Lymphoma)(3S A Review of Breast Implant-Associated Anaplastic Large Cell Lymphoma): p. 65S-73S., https://pubmed.ncbi.nlm.nih.gov/30817558/

1712. Möllhoff, N, Ehrl, D, Fuchs, B, Frank, K, Alt, V, Mayr, D, et.al. [Breast implant-associated squamous cell carcinoma: a systematic literature review]., Handchir Mikrochir Plast Chir, 2023. 55 (4)(4): p. 268-277., https://pubmed.ncbi.nlm.nih.gov/37473774/

1713. Ablatio mammae e.V., Selbstbewusst ohne Brust: Nach der Mastektomie. (n.d.), Retrieved September 10, 2024., https://amsob.de/

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1715. Aesthetic Flat Closure - Going Flat Photos & Resources - NPOAS. (n.d.)., Retrieved September 10, 2024., https://notputtingonashirt.org/whatisflatclosure/

1716. ‘Going Flat’ After Breast Cancer - The New York Times. (n.d.)., Retrieved September 10, 2024., https://www.nytimes.com/2016/11/01/well/live/going-flat-after-breast-cancer.html

1717. Resources for Providers - Oncoplastic Mastectomy - Aesthetic Flat Closure - NPOAS. (n.d.)., Retrieved September 9, 2024., https://notputtingonashirt.org/providers/#Articles

1718. Baker, JL, The Era of Flat Closure Mastectomy (Is Still Here). Are You Ready?, Ann Surg Oncol, 2023. 30 (11)(11): p. 6293-6295., https://pubmed.ncbi.nlm.nih.gov/37587363/

1719. Johnson, MK, Cortina, CS, Hsu, TL, Huang, S, Frebault, J, Huang, CC, et.al. National Trends in "Going Flat" After Mastectomy., Ann Surg Oncol, 2023. 30 (11)(11): p. 6374-6382., https://pubmed.ncbi.nlm.nih.gov/37458947/

1720. Crown, A, Buchanan, C, My surgical practice: Presenting aesthetic flat closure as an equal option to mastectomy with reconstruction and technical considerations to optimize cosmesis., Am J Surg, 2022. 223 (2)(2): p. 436-437., https://pubmed.ncbi.nlm.nih.gov/34412900/

1721. Klenotic, E., Ochoa, D., Stephenson, K., Croswell, C., Sullivan, S., Sherman, A., et.al. Flat Aesthetic Mastectomy Closure with the Angel Wing Technique to Address Lateral Adiposity: Technique and Outcome Analysis, 2024/03/25. 2024:, https://pubmed.ncbi.nlm.nih.gov/39742365/

1722. Morrison, KA, Karp, NS, Not Just a Linear Closure: Aesthetic Flat Closure after Mastectomy., Plast Reconstr Surg Glob Open, 2022. 10 (5)(5): p. e4327., https://pubmed.ncbi.nlm.nih.gov/35620492/

1723. Tyner, TE, Lee, MA, Satisfaction Outcomes in Women Who "Choose to Go Flat" After Mastectomy: An Integrative Review., ANS Adv Nurs Sci 44 (1)(1): p. 31-51., https://pubmed.ncbi.nlm.nih.gov/32956091/

1724. Baker, JL, Dizon, DS, Wenziger, CM, Streja, E, Thompson, CK, Lee, MK, et.al. "Going Flat" After Mastectomy: Patient-Reported Outcomes by Online Survey., Ann Surg Oncol, 2021. 28 (5)(5): p. 2493-2505., https://pubmed.ncbi.nlm.nih.gov/33393025/

1725. Baker, JL, Attai, DJ, ASO Author Reflections: Patients Who Go Flat After Mastectomy Deserve an Aesthetic Flat Closure., Ann Surg Oncol, 2021. 28 (5)(5): p. 2506., https://pubmed.ncbi.nlm.nih.gov/33475882/

1726. Wakeley, ME, Bare, CF, Pine, R, Dube, C, Gass, JS, Taneja, C, et.al. A social media survey of women who do not pursue reconstruction after mastectomy for breast cancer: Characterizing the "Going Flat" movement., Breast J, 2020. 26 (7)(7): p. 1455-1457., https://pubmed.ncbi.nlm.nih.gov/32067326/

1727. van der Wielen, A, Negenborn, V, Burchell, GL, Remmelzwaal, S, Lapid, O, Driessen, C, Less is more? One-stage versus two-stage implant-based breast reconstruction: A systematic review and meta-analysis of comparative studies., J Plast Reconstr Aesthet Surg, 2023. 86 (): p. 109-127., https://pubmed.ncbi.nlm.nih.gov/37716248/

1728. Aliotta, RE, Duraes, EFR, Scomacao, I, Morisada, M, Orra, S, Moreira, A, et.al. A controlled cost and outcomes analysis of acellular dermal matrix and implant-based reconstruction., J Plast Reconstr Aesthet Surg, 2021. 74 (6)(6): p. 1229-1238., https://pubmed.ncbi.nlm.nih.gov/33526361/

1729. Azouz, V, Lopez, S, Wagner, DS, Surgeon-Controlled Comparison of Direct-to-Implant and 2-Stage Tissue Expander-Implant Immediate Breast Reconstruction Outcomes., Ann Plast Surg, 2018. 80 (3)(3): p. 212-216., https://pubmed.ncbi.nlm.nih.gov/28984661/

1730. Bennett, KG, Qi, J, Kim, HM, Hamill, JB, Pusic, AL, Wilkins, EG, Comparison of 2-Year Complication Rates Among Common Techniques for Postmastectomy Breast Reconstruction., JAMA Surg, 2018. 153 (10)(10): p. 901-908., https://pubmed.ncbi.nlm.nih.gov/29926077/

1731. Caputo, GG, Vigato, E, Rampino Cordaro, E, Parodi, PC, Governa, M, Comparative study of patient outcomes between direct to implant and two-stage implant-based breast reconstruction after mastectomy., J Plast Reconstr Aesthet Surg, 2021. 74 (10)(10): p. 2573-2579., https://pubmed.ncbi.nlm.nih.gov/33947651/

1732. Casella, D, Di Taranto, G, Onesti, MG, Greco, M, Ribuffo, D, A retrospective comparative analysis of risk factors and outcomes in direct-to-implant and two-stages prepectoral breast reconstruction: BMI and radiotherapy as new selection criteria of patients., Eur J Surg Oncol, 2019. 45 (8)(8): p. 1357-1363., https://pubmed.ncbi.nlm.nih.gov/30827802/

1733. Damen, TH, Wei, W, Mureau, MA, Tjong-Joe-Wai, R, Hofer, SO, Essink-Bot, ML, et.al. Medium-term cost analysis of breast reconstructions in a single Dutch centre: a comparison of implants, implants preceded by tissue expansion, LD transpositions and DIEP flaps., J Plast Reconstr Aesthet Surg, 2011. 64 (8)(8): p. 1043-53., https://pubmed.ncbi.nlm.nih.gov/21317054/

1734. Davila, AA, Mioton, LM, Chow, G, Wang, E, Merkow, RP, Bilimoria, KY, et.al. Immediate two-stage tissue expander breast reconstruction compared with one-stage permanent implant breast reconstruction: a multi-institutional comparison of short-term complications., J Plast Surg Hand Surg, 2013. 47 (5)(5): p. 344-9., https://pubmed.ncbi.nlm.nih.gov/23547540/

1735. Dikmans, RE, Negenborn, VL, Bouman, MB, Winters, HA, Twisk, JW, Ruhé, PQ, et.al. Two-stage implant-based breast reconstruction compared with immediate one-stage implant-based breast reconstruction augmented with an acellular dermal matrix: an open-label, phase 4, multicentre, randomised, controlled trial., Lancet Oncol, 2017. 18 (2)(2): p. 251-258., https://pubmed.ncbi.nlm.nih.gov/28012977/

1736. Dimovska, EOF, Chen, C, Chou, HH, Lin, YL, Cheng, MH, Outcomes and quality of life in immediate one-stage versus two-stage breast reconstructions without an acellular dermal matrix: 17- years of experience., J Surg Oncol, 2021. 124 (4)(4): p. 510-520., https://pubmed.ncbi.nlm.nih.gov/34133023/

1737. Gao, P, Bai, P, Ren, Y, Kong, X, Wang, Z, Fang, Y, et.al. Biological Matrix-Assisted One-Stage Implant-Based Breast Reconstruction Versus Two-Stage Implant-Based Breast Reconstruction: Patient-Reported Outcomes and Complications., Aesthetic Plast Surg, 2021. 45 (6)(6): p. 2581-2590., https://pubmed.ncbi.nlm.nih.gov/34350500/

1738. Hangge, PT, Jogerst, K, Mohsen, A, Kosiorek, H, Cronin, PA, Stucky, CH, et.al. Making an informed choice: Which breast reconstruction type has the lowest complication rate?, Am J Surg, 2019. 218 (6)(6): p. 1040-1045., https://pubmed.ncbi.nlm.nih.gov/31606126/

1739. Hillberg, NS, Ferdinandus, PI, Dikmans, REG, Winkens, B, Hommes, J, van der Hulst, RRWJ, Is single-stage implant-based breast reconstruction (SSBR) with an acellular matrix safe?: Strattice™ or Meso Biomatrix® in SSBR., Eur J Plast Surg, 2018. 41 (4)(4): p. 429-438., https://pubmed.ncbi.nlm.nih.gov/30100676/

1740. Hwang, YJ, Lee, HC, Park, SH, Yoon, ES, A Comparative Study of Breast Sensibility and Patient Satisfaction After Breast Reconstruction: Autologous, 2-Stage Implant-Based, and Prepectoral Direct-to-Implant Reconstruction., Ann Plast Surg, 2022. 88 (3)(3): p. 262-270., https://pubmed.ncbi.nlm.nih.gov/35130204/

1741. Innocenti, A, Melita, D, Affortunati, M, Susini, T, Innocenti, M, Immediate-implant-based-breast-reconstruction with two-stage expander-implant reconstruction versus one-stage-reconstruction with acellular dermal matrix: analysis of patients' satisfaction., Acta Biomed, 2021. 92 (3)(3): p. e2021228., https://pubmed.ncbi.nlm.nih.gov/34212931/

1742. Meshulam-Derazon, S, Shay, T, Lewis, S, Adler, N, Immediate Breast Reconstruction: Comparative Outcome Study of One-Stage Direct-to-Implant and Two-Stage/Tissue Expander Techniques., Isr Med Assoc J, 2018. 20 (6)(6): p. 340-344., https://pubmed.ncbi.nlm.nih.gov/29911752/

1743. Negenborn, VL, Young-Afat, DA, Dikmans, REG, Smit, JM, Winters, HAH, Don Griot, JPW, et.al. Quality of life and patient satisfaction after one-stage implant-based breast reconstruction with an acellular dermal matrix versus two-stage breast reconstruction (BRIOS): primary outcome of a randomised, controlled trial., Lancet Oncol, 2018. 19 (9)(9): p. 1205-1214., https://pubmed.ncbi.nlm.nih.gov/30104147/

1744. Negenborn, VL, Smit, JM, Dikmans, REG, Winters, HAH, Twisk, JWR, Ruhé, PQ, et.al. Short-term cost-effectiveness of one-stage implant-based breast reconstruction with an acellular dermal matrix versus two-stage expander-implant reconstruction from a multicentre randomized clinical trial., Br J Surg, 2019. 106 (5)(5): p. 586-595., https://pubmed.ncbi.nlm.nih.gov/30835827/

1745. Riggio, E, Alfieri, S, Toffoli, E, Borreani, C, A descriptive comparison of satisfaction and well-being between expander-based and direct-to-implant breast reconstruction after Nipple-Sparing Mastectomy., Aesthetic Plast Surg, 2023. 47 (1)(1): p. 30-39., https://pubmed.ncbi.nlm.nih.gov/36018329/

1746. Roostaeian, J, Sanchez, I, Vardanian, A, Herrera, F, Galanis, C, Da Lio, A, et.al. Comparison of immediate implant placement versus the staged tissue expander technique in breast reconstruction., Plast Reconstr Surg, 2012. 129 (6)(6): p. 909e-918e., https://pubmed.ncbi.nlm.nih.gov/22634689/

1747. Sgarzani, R, Pasquali, S, Buggi, F, Tognali, D, Marongiu, F, Mingozzi, M, et.al. Sub-muscular Reconstruction after NAC Sparing Mastectomy: Direct to Implant Breast Reconstruction with Human ADM Versus Tissue Expander., Aesthetic Plast Surg, 2021. 45 (2)(2): p. 413-420., https://pubmed.ncbi.nlm.nih.gov/33078212/

1748. Susarla, SM, Ganske, I, Helliwell, L, Morris, D, Eriksson, E, Chun, YS, Comparison of clinical outcomes and patient satisfaction in immediate single-stage versus two-stage implant-based breast reconstruction., Plast Reconstr Surg, 2015. 135 (1)(1): p. 1e-8e., https://pubmed.ncbi.nlm.nih.gov/25539329/

1749. Theunissen, CIJM, Brohet, RM, Hu, Y, van Uchelen, JH, Mensen, JHC, van Rijssen, AL, Risk of breast implant removal after one- versus two-stage breast reconstructive surgery., J Plast Reconstr Aesthet Surg, 2022. 75 (5)(5): p. 1610-1616., https://pubmed.ncbi.nlm.nih.gov/34975002/

1750. Innocenti, Alessandro, Melita, Dario, Two-stage expander/implant breast reconstruction versus prepectoral breast reconstruction with acellular dermal matrix: a cost analysis, 2022. 45(4): p. 601 - 615., https://doi.org/10.1007/s00238-021-01829-x

1751. Han, HH, Kim, HB, Kim, EK, Eom, JS, Direct-to-Implant as a Frontline Option for Immediate Breast Reconstruction: A Comparative Study With 2-Stage Reconstruction., Ann Plast Surg, 2018. 81 (3)(3): p. 274-279., https://pubmed.ncbi.nlm.nih.gov/29916885/

1752. Damen, TH, Wei, W, Mureau, MA, Tjong-Joe-Wai, R, Hofer, SO, Essink-Bot, ML, et.al. Medium-term cost analysis of breast reconstructions in a single Dutch centre: a comparison of implants, implants preceded by tissue expansion, LD transpositions and DIEP flaps., J Plast Reconstr Aesthet Surg, 2011. 64 (8)(8): p. 1043-53., https://pubmed.ncbi.nlm.nih.gov/21317054/

1753. Negenborn, VL, Dikmans, REG, Bouman, MB, Winters, HAH, Twisk, JWR, Ruhé, PQ, et.al. Predictors of complications after direct-to-implant breast reconstruction with an acellular dermal matrix from a multicentre randomized clinical trial., Br J Surg, 2018. 105 (10)(10): p. 1305-1312., https://pubmed.ncbi.nlm.nih.gov/29663320/

1754. Beier, L, Faridi, A, Neumann, C, Paepke, S, Mau, C, Keller, M, et.al. Human Acellular Dermal Matrix (Epiflex®) in Immediate Implant-Based Breast Reconstruction after Skin- and Nipple-Sparing Mastectomy and Treatment of Capsular Fibrosis: Results of a Multicenter, Prospective, Observational NOGGO-AWOGyn Study., Breast Care (Basel), 2021. 16 (5)(5): p. 461-467., https://pubmed.ncbi.nlm.nih.gov/34720805/

1755. Thill, M, Faridi, A, Meiré, A, Gerber-Schäfer, C, Baumann, K, Blohmer, JU, et.al. Patient reported outcome and cosmetic evaluation following implant-based breast-reconstruction with a titanized polypropylene mesh (TiLOOP® Bra): A prospective clinical study in 269 patients., Eur J Surg Oncol, 2020. 46 (8)(8): p. 1484-1490., https://pubmed.ncbi.nlm.nih.gov/32336622/

1756. Weinzierl, A, Schmauss, D, Brucato, D, Harder, Y, Implant-Based Breast Reconstruction after Mastectomy, from the Subpectoral to the Prepectoral Approach: An Evidence-Based Change of Mind?, J Clin Med, 2022. 11 (11)(11):, https://pubmed.ncbi.nlm.nih.gov/35683465/

1757. Cook, H, Zargaran, D, Glynou, SP, Hamilton, S, Mosahebi, A, Does the use of acellular dermal matrices (ADM) in women undergoing pre-pectoral implant-based breast reconstruction increase operative success versus non-use of ADM in the same setting? A systematic review protocol., Syst Rev, 2024. 13 (1)(1): p. 153., https://pubmed.ncbi.nlm.nih.gov/38849880/

1758. Kappos, EA, Schulz, A, Regan, MM, Moffa, G, Harder, Y, Ribi, K, et.al. Prepectoral versus subpectoral implant-based breast reconstruction after skin-sparing mastectomy or nipple-sparing mastectomy (OPBC-02/ PREPEC): a pragmatic, multicentre, randomised, superiority trial., BMJ Open, 2021. 11 (9)(9): p. e045239., https://pubmed.ncbi.nlm.nih.gov/34475143/

1759. Micco, Rosa Di, Banys-Paluchowski, Maggie, Cardoso, Maria-Joao, de Boniface, Jana, Gulluoglu, Bahadir M., Kaidar-Person, Orit, et.al. Abstract PO5-19-02: I-PREPARE: International Prospective REgistry on Pre-pectorAl breast Reconstruction (EUBREAST 11R-NCT 05817175), 2024. 84(9_Supplement): p. PO5-19-02 - PO5-19-02., https://doi.org/10.1158/1538-7445.SABCS23-PO5-19-02

1760. Du, F, Liu, R, Zhang, H, Xiao, Y, Long, X, Post-mastectomy adjuvant radiotherapy for direct-to-implant and two-stage implant-based breast reconstruction: A meta-analysis., J Plast Reconstr Aesthet Surg, 2022. 75 (9)(9): p. 3030-3040., https://pubmed.ncbi.nlm.nih.gov/35961927/

1761. Allué Cabañuz, M, Arribas Del Amo, MD, Navarro Barlés, A, Guemes Sanchez, AT, Influence of radiotherapy on immediate breast reconstruction after skin-sparing mastectomy. Before or after: Does it matter?, Cir Esp (Engl Ed), 2019. 97 (3)(3): p. 156-161., https://pubmed.ncbi.nlm.nih.gov/30545644/

1762. Apte, A, Walsh, M, Balaji, P, Khor, B, Chandrasekharan, S, Chakravorty, A, Single stage immediate breast reconstruction with acellular dermal matrix and implant: Defining the risks and outcomes of post-mastectomy radiotherapy., Surgeon, 2020. 18 (4)(4): p. 202-207., https://pubmed.ncbi.nlm.nih.gov/31636037/

1763. Cordeiro, PG, Albornoz, CR, McCormick, B, Hudis, CA, Hu, Q, Heerdt, A, et.al. What Is the Optimum Timing of Postmastectomy Radiotherapy in Two-Stage Prosthetic Reconstruction: Radiation to the Tissue Expander or Permanent Implant?, Plast Reconstr Surg, 2015. 135 (6)(6): p. 1509-1517., https://pubmed.ncbi.nlm.nih.gov/25742523/

1764. Hamann, M, Brunnbauer, M, Scheithauer, H, Hamann, U, Braun, M, Pölcher, M, Quality of life in breast cancer patients and surgical results of immediate tissue expander/implant-based breast reconstruction after mastectomy., Arch Gynecol Obstet, 2019. 300 (2)(2): p. 409-420., https://pubmed.ncbi.nlm.nih.gov/31144025/

1765. Hille-Betz, U, Kniebusch, N, Wojcinski, S, Henseler, H, Heyl, V, Ohlinger, R, et.al. Breast reconstruction and revision surgery for implant-associated breast deformities using porcine acellular dermal matrix: a multicenter study of 156 cases., Ann Surg Oncol, 2015. 22 (4)(4): p. 1146-52., https://pubmed.ncbi.nlm.nih.gov/25300607/

1766. Korwar, V, Skillman, J, Matey, P, Skin reducing mastectomy and immediate reconstruction: the effect of radiotherapy on complications and patient reported outcomes., Eur J Surg Oncol, 2014. 40 (4)(4): p. 442-8., https://pubmed.ncbi.nlm.nih.gov/24512987/

1767. Loreti, A, Siri, G, De Carli, M, Fanelli, B, Arelli, F, Spallone, D, et.al. Immediate Breast Reconstruction after mastectomy with polyurethane implants versus textured implants: A retrospective study with focus on capsular contracture., Breast, 2020. 54 (): p. 127-132., https://pubmed.ncbi.nlm.nih.gov/33010626/

1768. Masià, J, The largest multicentre data collection on prepectoral breast reconstruction: The iBAG study., J Surg Oncol, 2020. 122 (5)(5): p. 848-860., https://pubmed.ncbi.nlm.nih.gov/32786089/

1769. Naoum, GE, Salama, L, Niemierko, A, Vieira, BL, Belkacemi, Y, Colwell, AS, et.al. Single Stage Direct-to-Implant Breast Reconstruction Has Lower Complication Rates Than Tissue Expander and Implant and Comparable Rates to Autologous Reconstruction in Patients Receiving Postmastectomy Radiation., Int J Radiat Oncol Biol Phys, 2020. 106 (3)(3): p. 514-524., https://pubmed.ncbi.nlm.nih.gov/31756414/

1770. Riggio, E, Toffoli, E, Tartaglione, C, Marano, G, Biganzoli, E, Local safety of immediate reconstruction during primary treatment of breast cancer. Direct-to-implant versus expander-based surgery., J Plast Reconstr Aesthet Surg, 2019. 72 (2)(2): p. 232-242., https://pubmed.ncbi.nlm.nih.gov/30497914/

1771. Salzberg, CA, Ashikari, AY, Berry, C, Hunsicker, LM, Acellular Dermal Matrix-Assisted Direct-to-Implant Breast Reconstruction and Capsular Contracture: A 13-Year Experience., Plast Reconstr Surg, 2016. 138 (2)(2): p. 329-337., https://pubmed.ncbi.nlm.nih.gov/27064232/

1772. Seth, AK, Silver, HR, Hirsch, EM, Kim, JY, Fine, NA, Comparison of Delayed and Immediate Tissue Expander Breast Reconstruction in the Setting of Postmastectomy Radiation Therapy., Ann Plast Surg, 2015. 75 (5)(5): p. 503-7., https://pubmed.ncbi.nlm.nih.gov/25180955/

1773. Sinnott, CJ, Persing, SM, Pronovost, M, Hodyl, C, McConnell, D, Ott Young, A, Impact of Postmastectomy Radiation Therapy in Prepectoral Versus Subpectoral Implant-Based Breast Reconstruction., Ann Surg Oncol, 2018. 25 (10)(10): p. 2899-2908., https://pubmed.ncbi.nlm.nih.gov/29978367/

1774. Spear, SL, Seruya, M, Rao, SS, Rottman, S, Stolle, E, Cohen, M, et.al. Two-stage prosthetic breast reconstruction using AlloDerm including outcomes of different timings of radiotherapy., Plast Reconstr Surg, 2012. 130 (1)(1): p. 1-9., https://pubmed.ncbi.nlm.nih.gov/22743866/

1775. Tejera Hernández, AA, Vega Benítez, VM, Rocca Cardenas, JC, Ortega Pérez, N, Rodríguez Ibarria, N, Gutiérrez Giner, MI, et.al. Inverse radiotherapy planning in reconstructive surgery for breast cancer., Int J Surg, 2019. 63 (): p. 77-82., https://pubmed.ncbi.nlm.nih.gov/30708063/

1776. Coudé Adam, H, Frisell, A, Liu, Y, Sackey, H, Oikonomou, I, Docherty Skogh, AC, et.al. Effect of radiotherapy on expanders and permanent implants in immediate breast reconstruction: long-term surgical and patient-reported outcomes in a large multicentre cohort., Br J Surg, 2021. 108 (12)(12): p. 1474-1482., https://pubmed.ncbi.nlm.nih.gov/34694356/

1777. Bernini, M, Meattini, I, Saieva, C, Becherini, C, Salvestrini, V, Visani, L, et.al. Pre-pectoral breast reconstruction: early and long-term safety evaluation of 146 unselected cases of the early pre-pectoral era of a single-institution, including cases with previous breast irradiation and post-mastectomy radiation therapy., Breast Cancer, 2022. 29 (2)(2): p. 302-313., https://pubmed.ncbi.nlm.nih.gov/34775540/

1778. Cagli, B, Morelli Coppola, M, Augelli, F, Segreto, F, Tenna, S, Cogliandro, A, et.al. Postmastectomy Radiation Therapy in the Setting of Two-Stage Retropectoral Implant-Based Breast Reconstruction: Should It be Delivered Before or After Implant Exchange? A Retrospective Analysis on 183 Patients., Aesthetic Plast Surg, 2022. 46 (6)(6): p. 2643-2654., https://pubmed.ncbi.nlm.nih.gov/35854008/

1779. de Boniface, J, Coudé Adam, H, Frisell, A, Oikonomou, I, Ansarei, D, Ljung Konstantinidou, A, et.al. Long-term outcomes of implant-based immediate breast reconstruction with and without radiotherapy: a population-based study., Br J Surg, 2022. 109 (11)(11): p. 1107-1115., https://pubmed.ncbi.nlm.nih.gov/35949111/

1780. Conte, B, Shermoen, C, Lubarsky, M, Fiser, CK, Liu, SN, Kesmodel, SB, et.al. Post-Mastectomy Implant Complications in the Hispanic Breast Cancer Patient Population., Anticancer Res, 2023. 43 (11)(11): p. 4953-4959., https://pubmed.ncbi.nlm.nih.gov/37909997/

1781. Jeon, HB, Lee, M, Roh, TS, Jeong, J, Ahn, SG, Bae, SJ, et.al. Complications Including Capsular Contracture in Direct-to-Implant Breast Reconstruction With Textured Anatomical Versus Smooth Round Implants: A Single Center Retrospective Analysis., J Breast Cancer, 2023. 26 (1)(1): p. 25-34., https://pubmed.ncbi.nlm.nih.gov/36852965/

1782. Kooijman, MML, Hage, JJ, Scholten, AN, Vrancken Peeters, MTFD, Woerdeman, LAE, Short-Term Surgical Complications of Skin-Sparing Mastectomy and Direct-to-Implant Immediate Breast Reconstruction in Women Concurrently Treated with Adjuvant Radiotherapy for Breast Cancer., Arch Plast Surg, 2022. 49 (3)(3): p. 332-338., https://pubmed.ncbi.nlm.nih.gov/35832162/

1783. Lee, KT, Kim, J, Jeon, BJ, Pyon, JK, Bang, SI, Mun, GH, Longitudinal analysis of long-term outcomes of abdominal flap-based microsurgical reconstruction and two-stage prosthetic reconstruction., Sci Rep, 2023. 13 (1)(1): p. 4062., https://pubmed.ncbi.nlm.nih.gov/36906629/

1784. Martins, LL, Barbosa, RF, Guerreiro, FC, Andresen, C, Pereira, MJ, Pinho, CJ, et.al. A Two-Year Retrospective Analysis of the Clinical Outcomes of Immediate Submuscular Breast Reconstructions With Native® Acellular Dermal Matrix., Cureus, 2023. 15 (7)(7): p. e41343., https://pubmed.ncbi.nlm.nih.gov/37546031/

1785. Naoum, GE, Ioakeim, MI, Shui, AM, Salama, L, Colwell, A, Ho, AY, et.al. Radiation Modality (Proton/Photon), Timing, and Complication Rates in Patients With Breast Cancer Receiving 2-Stages Expander/Implant Reconstruction., Pract Radiat Oncol, 2022. 12 (6)(6): p. 475-486., https://pubmed.ncbi.nlm.nih.gov/35989216/

1786. Nelson, JA, Cordeiro, PG, Polanco, T, Shamsunder, MG, Patel, A, Allen, RJ, et.al. Association of Radiation Timing with Long-Term Satisfaction and Health-Related Quality of Life in Prosthetic Breast Reconstruction., Plast Reconstr Surg, 2022. 150 (1)(1): p. 32e-41e., https://pubmed.ncbi.nlm.nih.gov/35499580/

1787. Ostapenko, E, Nixdorf, L, Devyatko, Y, Exner, R, Wimmer, K, Fitzal, F, The Impact of Adjuvant Radiotherapy on Immediate Prepectoral Implant-Based Breast Reconstruction., Aesthetic Plast Surg, 2024. 48 (13)(13): p. 2432-2438., https://pubmed.ncbi.nlm.nih.gov/37737875/

1788. Polotto, S, Pedrazzi, G, Bergamini, M, D'Abbiero, N, Cattelani, L, ADM-Assisted Direct-to-Implant Prepectoral Breast Reconstruction in Postmastectomy Radiation Therapy Setting: Long-Term Results., Clin Breast Cancer, 2023. 23 (7)(7): p. 704-711., https://pubmed.ncbi.nlm.nih.gov/37479666/

1789. Safran, T, Al-Badarin, F, Al-Halabi, B, Viezel-Mathieu, A, Dionisopoulos, T, Aesthetic Limitations in Direct-to-Implant Prepectoral Breast Reconstruction., Plast Reconstr Surg, 2022. 150 (1)(1): p. 22e-31e., https://pubmed.ncbi.nlm.nih.gov/35499675/

1790. Saksornchai, K, Ganoksil, P, Rongkavilit, S, Suwajo, P, Impact of radiation on immediate breast reconstruction: a retrospective single institution cohort study., Gland Surg, 2023. 12 (8)(8): p. 1050-1059., https://pubmed.ncbi.nlm.nih.gov/37701294/

1791. Sewart, E, Turner, NL, Conroy, EJ, Cutress, RI, Skillman, J, Whisker, L, et.al. The Impact of Radiotherapy on Patient-reported Outcomes of Immediate Implant-based Breast Reconstruction With and Without Mesh., Ann Surg, 2022. 275 (5)(5): p. 992-1001., https://pubmed.ncbi.nlm.nih.gov/32657919/

1792. Stuart, SR, Munhoz, AM, Chaves, CLG, Montag, E, Cordeiro, TCS, Fuzisaki, TT, et.al. Complications after breast reconstruction with alloplastic material in breast cancer patients submitted or not to post mastectomy radiotherapy., Rep Pract Oncol Radiother, 2021. 26 (5)(5): p. 730-739., https://pubmed.ncbi.nlm.nih.gov/34760307/

1793. Sun, L, Zhu, W, Zhang, J, Zhong, B, Li, S, Li, H, et.al. The risk factors and the relationship between radiation dose and complications and prosthetic reconstruction failure in patients with post-mastectomy breast implant reconstruction: a retrospective cohort study., Gland Surg, 2022. 11 (11)(11): p. 1817-1831., https://pubmed.ncbi.nlm.nih.gov/36518801/

1794. Yin, Z, Wang, H, Liu, Y, Wang, Y, Chang, EI, Yin, J, Single-Institution Algorithm for Prevention and Management of Complications in Direct-to-Implant Breast Reconstruction., Plast Reconstr Surg, 2022. 150 (): p. 48S-60S., https://pubmed.ncbi.nlm.nih.gov/35943963/

1795. Dave, RV, Vucicevic, A, Barrett, E, Highton, L, Johnson, R, Kirwan, CC, et.al. Risk factors for complications and implant loss after prepectoral implant-based immediate breast reconstruction: medium-term outcomes in a prospective cohort., Br J Surg, 2021. 108 (5)(5): p. 534-541., https://pubmed.ncbi.nlm.nih.gov/34043774/

1796. Emanuele Lisa, AV, Salgarello, M, Huscher, A, Corsi, F, Piovani, D, Rubbino, F, et.al. The Effect of Adjuvant Radiotherapy on One- and Two-Stage Prosthetic Breast Reconstruction and on Autologous Reconstruction: A Multicenter Italian Study among 18 Senonetwork Breast Centres., Breast J, 2023. 2023 (): p. 6688466., https://pubmed.ncbi.nlm.nih.gov/37205012/

1797. Pires, G, Marquez, JL, Memmott, S, Sudduth, JD, Moss, W, Eddington, D, et.al. Early Complications after Prepectoral Tissue Expander Placement in Breast Reconstruction with and without Acellular Dermal Matrix., Plast Reconstr Surg, 2024. 153 (6)(6): p. 1221-1229., https://pubmed.ncbi.nlm.nih.gov/37285211/

1798. Lin, AM, Lorenzi, R, Van Der Hulst, JE, Liao, EC, Austen, WG, Webster, A, et.al. A Decade of Nipple-Sparing Mastectomy: Lessons Learned in 3035 Immediate Implant-Based Breast Reconstructions., Plast Reconstr Surg, 2024. 153 (2)(2): p. 277-287., https://pubmed.ncbi.nlm.nih.gov/37141449/

1799. Nava, MB, Pennati, AE, Lozza, L, Spano, A, Zambetti, M, Catanuto, G, Outcome of different timings of radiotherapy in implant-based breast reconstructions., Plast Reconstr Surg, 2011. 128 (2)(2): p. 353-359., https://pubmed.ncbi.nlm.nih.gov/21788827/

1800. Emanuele Lisa, AV, Salgarello, M, Huscher, A, Corsi, F, Piovani, D, Rubbino, F, et.al. The Effect of Adjuvant Radiotherapy on One- and Two-Stage Prosthetic Breast Reconstruction and on Autologous Reconstruction: A Multicenter Italian Study among 18 Senonetwork Breast Centres., Breast J, 2023. 2023 (): p. 6688466., https://pubmed.ncbi.nlm.nih.gov/37205012/

1801. Nelson, JA, Cordeiro, PG, Polanco, T, Shamsunder, MG, Patel, A, Allen, RJ, et.al. Association of Radiation Timing with Long-Term Satisfaction and Health-Related Quality of Life in Prosthetic Breast Reconstruction., Plast Reconstr Surg, 2022. 150 (1)(1): p. 32e-41e., https://pubmed.ncbi.nlm.nih.gov/35499580/

1802. Jagsi, R, Li, Y, Morrow, M, Janz, N, Alderman, A, Graff, J, et.al. Patient-reported Quality of Life and Satisfaction With Cosmetic Outcomes After Breast Conservation and Mastectomy With and Without Reconstruction: Results of a Survey of Breast Cancer Survivors., Ann Surg, 2015. 261 (6)(6): p. 1198-206., https://pubmed.ncbi.nlm.nih.gov/25654742/

1803. Ren, Y, Yu, Y, Xu, K, Li, Z, Wang, X, Meta-Analysis of Immediate Implant-Based Breast Reconstruction Versus Autologous Breast Reconstruction in the Setting of PMRT., Aesthetic Plast Surg, 2024. 48 (10)(10): p. 1940-1948., https://pubmed.ncbi.nlm.nih.gov/37380747/

1804. Matar, DY, Wu, M, Haug, V, Orgill, DP, Panayi, AC, Surgical complications in immediate and delayed breast reconstruction: A systematic review and meta-analysis., J Plast Reconstr Aesthet Surg, 2022. 75 (11)(11): p. 4085-4095., https://pubmed.ncbi.nlm.nih.gov/36202732/

1805. Barnes, LL, Patterson, A, Lem, M, Holland, MC, Lentz, R, Sbitany, H, et.al. Immediate Versus Delayed-Immediate Autologous Breast Reconstruction After Nipple-Sparing Mastectomy., Ann Plast Surg, 2023. 90 (5)(5): p. 432-436., https://pubmed.ncbi.nlm.nih.gov/37146309;, 34921369;, 36928907;, 35245253;, 34270511;, 35135030;, 34028673;, 36474094;, 35796741/

1806. Shammas, RL, Cason, RW, Sergesketter, AR, Glener, AD, Broadwater, G, Hollins, A, et.al. A Comparison of Surgical Complications in Patients Undergoing Delayed versus Staged Tissue-Expander and Free-Flap Breast Reconstruction., Plast Reconstr Surg, 2021. 148 (3)(3): p. 501-509., https://pubmed.ncbi.nlm.nih.gov/34270511/

1807. Shammas, RL, Gordee, A, Lee, HJ, Sergesketter, AR, Scales, CD, Hollenbeck, ST, et.al. Complications, Costs, and Healthcare Resource Utilization After Staged, Delayed, and Immediate Free-Flap Breast Reconstruction: A Longitudinal, Claims-Based Analysis., Ann Surg Oncol, 2023. 30 (4)(4): p. 2534-2549., https://pubmed.ncbi.nlm.nih.gov/36474094/

1808. Pittelkow, E, DeBrock, W, Christopher, L, Mercho, R, Suh, LJ, Fisher, CS, et.al. Advantages of the Delayed-Immediate Microsurgical Breast Reconstruction: Extending the Choice., J Reconstr Microsurg, 2022. 38 (7)(7): p. 579-584., https://pubmed.ncbi.nlm.nih.gov/35135030/

1809. Joosen, MEM, Schop, SJ, Reinhoudt, LL, van Kuijk, SMJ, Beugels, J, de Bruïne, AP, et.al. The difference in local, regional and distant breast cancer recurrence between the immediate and delayed DIEP flap procedure; a retrospective cohort study., Breast Cancer Res Treat, 2021. 188 (2)(2): p. 389-398., https://pubmed.ncbi.nlm.nih.gov/34028673/

1810. Christopher, AN, Morris, MP, Broach, RB, Serletti, JM, A Comparative Analysis of Immediate and Delayed-immediate Breast Reconstruction after Postmastectomy Radiation Therapy., J Reconstr Microsurg, 2022. 38 (6)(6): p. 499-505., https://pubmed.ncbi.nlm.nih.gov/34921369/

1811. Ochoa, O, Garza, R, Pisano, S, Chrysopoulo, M, Ledoux, P, Arishita, G, et.al. Prospective Longitudinal Patient-Reported Satisfaction and Health-Related Quality of Life following DIEP Flap Breast Reconstruction: Effects of Reconstruction Timing., Plast Reconstr Surg, 2022. 149 (5)(5): p. 848e-857e., https://pubmed.ncbi.nlm.nih.gov/35245253/

1812. Marquez, JL, Sudduth, JD, Kuo, K, Patel, AA, Eddington, D, Agarwal, JP, et.al. A Comparison of Postoperative Outcomes Between Immediate, Delayed Immediate, and Delayed Autologous Free Flap Breast Reconstruction: Analysis of 2010-2020 NSQIP Data., J Reconstr Microsurg, 2023. 39 (8)(8): p. 664-670., https://pubmed.ncbi.nlm.nih.gov/36928907/

1813. Wu Young, MY, Garza, RM, Chang, DW, "Immediate versus delayed autologous breast reconstruction in patients undergoing post-mastectomy radiation therapy: A paradigm shift"., J Surg Oncol, 2022. 126 (6)(6): p. 949-955., https://pubmed.ncbi.nlm.nih.gov/35796741/

1814. Beugels, J, Bod, L, van Kuijk, SMJ, Qiu, SS, Tuinder, SMH, Heuts, EM, et.al. Complications following immediate compared to delayed deep inferior epigastric artery perforator flap breast reconstructions., Breast Cancer Res Treat, 2018. 169 (2)(2): p. 349-357., https://pubmed.ncbi.nlm.nih.gov/29399731/

1815. DeBono, R, Thompson, A, Stevenson, JH, Immediate versus delayed free TRAM breast reconstruction: an analysis of perioperative factors and complications., Br J Plast Surg, 2002. 55 (2)(2): p. 111-6., https://pubmed.ncbi.nlm.nih.gov/11987942/

1816. Chang, EI, Chang, EI, Soto-Miranda, MA, Zhang, H, Nosrati, N, Ghali, S, et.al. Evolution of Bilateral Free Flap Breast Reconstruction over 10 Years: Optimizing Outcomes and Comparison to Unilateral Reconstruction., Plast Reconstr Surg, 2015. 135 (6)(6): p. 946e-953e., https://pubmed.ncbi.nlm.nih.gov/26017610/

1817. Dewael, S, Vandevoort, M, Fabré, G, Nanhekhan, L, Immediate versus delayed autologous breast reconstruction: A retrospective matched cohort study of irradiated patients., J Plast Reconstr Aesthet Surg, 2019. 72 (11)(11): p. 1769-1775., https://pubmed.ncbi.nlm.nih.gov/31235319/

1818. Prantl, L, Moellhoff, N, von Fritschen, U, Giunta, RE, Germann, G, Kehrer, A, et.al. Immediate versus secondary DIEP flap breast reconstruction: a multicenter outcome study., Arch Gynecol Obstet, 2020. 302 (6)(6): p. 1451-1459., https://pubmed.ncbi.nlm.nih.gov/32895743/

1819. Manyam, BV, Shah, C, Woody, NM, Reddy, CA, Weller, MA, Juloori, A, et.al. Long-Term Outcomes After Autologous or Tissue Expander/Implant-Based Breast Reconstruction and Postmastectomy Radiation for Breast Cancer., Pract Radiat Oncol, 2019. 9 (6)(6): p. e497-e505., https://pubmed.ncbi.nlm.nih.gov/31238166/

1820. Sternberg, EG, Perdikis, G, McLaughlin, SA, Terkonda, SP, Waldorf, JC, Latissimus dorsi flap remains an excellent choice for breast reconstruction., Ann Plast Surg, 2006. 56 (1)(1): p. 31-5., https://pubmed.ncbi.nlm.nih.gov/16374092/

1821. Maalouf, C, Bou-Merhi, J, Karam, E, Patocskai, E, Danino, AM, The impact of autologous breast reconstruction using DIEP flap on the oncologic efficacy of radiation therapy., Ann Chir Plast Esthet, 2017. 62 (6)(6): p. 630-636., https://pubmed.ncbi.nlm.nih.gov/28760638/

1822. Tran, NV, Chang, DW, Gupta, A, Kroll, SS, Robb, GL, Comparison of immediate and delayed free TRAM flap breast reconstruction in patients receiving postmastectomy radiation therapy., Plast Reconstr Surg, 2001. 108 (1)(1): p. 78-82., https://pubmed.ncbi.nlm.nih.gov/11420508/

1823. Yoon, AP, Qi, J, Brown, DL, Kim, HM, Hamill, JB, Erdmann-Sager, J, et.al. Outcomes of immediate versus delayed breast reconstruction: Results of a multicenter prospective study., Breast, 2018. 37 (): p. 72-79., https://pubmed.ncbi.nlm.nih.gov/29102781/

1824. Zhong, T, Hu, J, Bagher, S, Vo, A, O'Neill, AC, Butler, K, et.al. A Comparison of Psychological Response, Body Image, Sexuality, and Quality of Life between Immediate and Delayed Autologous Tissue Breast Reconstruction: A Prospective Long-Term Outcome Study., Plast Reconstr Surg, 2016. 138 (4)(4): p. 772-780., https://pubmed.ncbi.nlm.nih.gov/27673514/

1825. Khajuria, A, Charles, WN, Prokopenko, M, Beswick, A, Pusic, AL, Mosahebi, A, et.al. Immediate and delayed autologous abdominal microvascular flap breast reconstruction in patients receiving adjuvant, neoadjuvant or no radiotherapy: a meta-analysis of clinical and quality-of-life outcomes., BJS Open, 2020. 4 (2)(2): p. 182-196., https://pubmed.ncbi.nlm.nih.gov/32207573/

1826. Kronowitz, SJ, Kuerer, HM, Advances and surgical decision-making for breast reconstruction., Cancer, 2006. 107 (5)(5): p. 893-907., https://pubmed.ncbi.nlm.nih.gov/16862569/

1827. Hsieh, WC, Tee, R, Huang, YT, Kuo, WL, Huang, JJ, Surgical and patient-reported outcomes in an Asian female population with or without adjuvant radiotherapy after immediate free perforator flap breast reconstruction: A retrospective review., JPRAS Open, 2023. 38 (): p. 237-248., https://pubmed.ncbi.nlm.nih.gov/38021323/

1828. Jagsi, R, Momoh, AO, Qi, J, Hamill, JB, Billig, J, Kim, HM, et.al. Impact of Radiotherapy on Complications and Patient-Reported Outcomes After Breast Reconstruction., J Natl Cancer Inst, 2018. 110 (2)(2): p. 157-65., https://pubmed.ncbi.nlm.nih.gov/28954300/

1829. Liew, B, Southall, C, Kanapathy, M, Nikkhah, D, Does post-mastectomy radiation therapy worsen outcomes in immediate autologous breast flap reconstruction? A systematic review and meta-analysis., J Plast Reconstr Aesthet Surg, 2021. 74 (12)(12): p. 3260-3280., https://pubmed.ncbi.nlm.nih.gov/34565703/

1830. Ly, CL, Khetpal, S, Heller, DR, Higgins, SA, Killelea, B, Alperovich, M, et.al. Comparing complications in irradiated and non-irradiated free-flaps in patients with bilateral immediate breast reconstruction and unilateral post-mastectomy radiotherapy., Microsurgery, 2021. 41 (7)(7): p. 615-621., https://pubmed.ncbi.nlm.nih.gov/33886127/

1831. Williams, JK, Carlson, GW, Bostwick, J, Bried, JT, Mackay, G, The effects of radiation treatment after TRAM flap breast reconstruction., Plast Reconstr Surg, 1997. 100 (5)(5): p. 1153-60., https://pubmed.ncbi.nlm.nih.gov/9326776/

1832. Tran, NV, Evans, GR, Kroll, SS, Baldwin, BJ, Miller, MJ, Reece, GP, et.al. Postoperative adjuvant irradiation: effects on tranverse rectus abdominis muscle flap breast reconstruction., Plast Reconstr Surg, 2000. 106 (2)(2): p. 313-7; discussion 318-20., https://pubmed.ncbi.nlm.nih.gov/10946929/

1833. Rogers, NE, Allen, RJ, Radiation effects on breast reconstruction with the deep inferior epigastric perforator flap., Plast Reconstr Surg, 2002. 109 (6)(6): p. 1919-24; discussion 1925-6., https://pubmed.ncbi.nlm.nih.gov/11994594/

1834. Spear, SL, Ducic, I, Low, M, Cuoco, F, The effect of radiation on pedicled TRAM flap breast reconstruction: outcomes and implications., Plast Reconstr Surg, 2005. 115 (1)(1): p. 84-95., https://pubmed.ncbi.nlm.nih.gov/15622237/

1835. Carlson, GW, Page, AL, Peters, K, Ashinoff, R, Schaefer, T, Losken, A, Effects of radiation therapy on pedicled transverse rectus abdominis myocutaneous flap breast reconstruction., Ann Plast Surg, 2008. 60 (5)(5): p. 568-72., https://pubmed.ncbi.nlm.nih.gov/18434833/

1836. Mirzabeigi, MN, Smartt, JM, Nelson, JA, Fosnot, J, Serletti, JM, Wu, LC, An assessment of the risks and benefits of immediate autologous breast reconstruction in patients undergoing postmastectomy radiation therapy., Ann Plast Surg, 2013. 71 (2)(2): p. 149-55., https://pubmed.ncbi.nlm.nih.gov/23542828/

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