Differences between screen-detected and interval breast cancers among BRCA mutation carriers

Author:

Pilewskie MelissaORCID,Zabor Emily C.,Gilbert Elizabeth,Stempel Michelle,Petruolo Oriana,Mangino Debra,Robson Mark,Jochelson Maxine S.

Funder

NIH/NCI Cancer Center Support Grant

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

Reference39 articles.

1. Chen S, Parmigiani G (2007) Meta-analysis of BRCA1 and BRCA2 penetrance. J Clin Oncol Off J Am Soc Clin Oncol 25(11):1329–1333. https://doi.org/10.1200/JCO.2006.09.1066

2. King MC, Marks JH, Mandell JB, New York Breast Cancer Study Group (2003) Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 302(5645):643–646. https://doi.org/10.1126/science.1088759

3. Kuchenbaecker KB, Hopper JL, Barnes DR, Phillips KA, Mooij TM, Roos-Blom MJ et al (2017) Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers. JAMA 317(23):2402–2416. https://doi.org/10.1001/jama.2017.7112

4. National Comprehensive Cancer Network (NCCN) NCCN clinical practice guidelines in oncology. BRCA-related breast and/or ovarian cancer syndrome. https://www.nccn.org . Accessed 30 Aug 2018

5. American Cancer Society (2015) American Cancer Society recommendations for the early detection of breast cancer. https://www.cancer.org/cancer/breast-cancer/screening-tests-and-early-detection/american-cancer-society-recommendations-for-the-early-detection-of-breast-cancer.html . Accessed 3 July 2018

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