Ten-Year Multi-Institutional Results of Breast-Conserving Surgery and Radiotherapy in BRCA1/2-Associated Stage I/II Breast Cancer

Author:

Pierce Lori J.1,Levin Albert M.1,Rebbeck Timothy R.1,Ben-David Merav A.1,Friedman Eitan1,Solin Lawrence J.1,Harris Eleanor E.1,Gaffney David K.1,Haffty Bruce G.1,Dawson Laura A.1,Narod Steven A.1,Olivotto Ivo A.1,Eisen Andrea1,Whelan Timothy J.1,Olopade Olufunmilayo I.1,Isaacs Claudine1,Merajver Sofia D.1,Wong Julia S.1,Garber Judy E.1,Weber Barbara L.1

Affiliation:

1. From the University of Michigan School of Medicine; University of Michigan School of Public Health, Ann Arbor, MI; Center for Clinical Epidemiology and Biostatistics and Abramson Family Cancer Research Institute, University of Pennsylvania; University of Pennsylvania School of Medicine, Philadelphia, PA; University of Utah School of Medicine, Salt Lake City, UT; UMDNJ-Robert Wood Johnson Medical School, New Brunswick, NJ; Lombardi Cancer Center, Georgetown University, Washington, DC; Dana-Farber Cancer...

Abstract

Purpose We compared the outcome of breast-conserving surgery and radiotherapy in BRCA1/2 mutation carriers with breast cancer versus that of matched sporadic controls. Methods A total of 160 BRCA1/2 mutation carriers with breast cancer were matched with 445 controls with sporadic breast cancer. Primary end points were rates of in-breast tumor recurrence (IBTR) and contralateral breast cancers (CBCs). Median follow-up was 7.9 years for mutation carriers and 6.7 years for controls. Results There was no significant difference in IBTR overall between carriers and controls; 10- and 15-year estimates were 12% and 24% for carriers and 9% and 17% for controls, respectively (hazard ratio [HR], 1.37; P = .19). Multivariate analyses for IBTR found BRCA1/2 mutation status to be an independent predictor of IBTR when carriers who had undergone oophorectomy were removed from analysis (HR, 1.99; P = .04); the incidence of IBTR in carriers who had undergone oophorectomy was not significantly different from that in sporadic controls (P = .37). CBCs were significantly greater in carriers versus controls, with 10- and 15-year estimates of 26% and 39% for carriers and 3% and 7% for controls, respectively (HR, 10.43; P < .0001). Tamoxifen use significantly reduced risk of CBCs in mutation carriers (HR, 0.31; P = .05). Conclusion IBTR risk at 10 years is similar in BRCA1/2 carriers treated with breast conservation surgery who undergo oophorectomy versus sporadic controls. As expected, CBCs are significantly increased in carriers. Although the incidence of CBCs was significantly reduced in mutation carriers who received tamoxifen, this rate remained significantly greater than in controls. Additional strategies are needed to reduce contralateral cancers in these high-risk women.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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