Germline Mutation in <i>BRCA1</i> or <i>BRCA2</i> and Ten-Year Survival for Women Diagnosed with Epithelial Ovarian Cancer

Francisco José Cândido dos Reis(Universidade de São Paulo), Honglin Song(Cancer Research UK Cambridge Center), Ellen L. Goode(Mayo Clinic), Julie M. Cunningham(Mayo Clinic), Brooke L. Fridley(University of Kansas Medical Center), Melissa C. Larson(Mayo Clinic), Kathryn Alsop(Peter MacCallum Cancer Centre), Ed Dicks(Cancer Research UK Cambridge Center), Patricia Harrington(Cancer Research UK Cambridge Center), Susan J. Ramus(University of Southern California), Anna de Fazio(Millennium Institute), Gillian Mitchell(Peter MacCallum Cancer Centre), Sián Fereday(Peter MacCallum Cancer Centre), Kelly L. Bolton(National Cancer Institute), Charlie Gourley(Edinburgh Cancer Research), Caroline O. Michie(Ninewells Hospital), Beth Y. Karlan(Cedars-Sinai Medical Center), Jenny Lester(Cedars-Sinai Medical Center), Christine Walsh(Cedars-Sinai Medical Center), Ilana Cass(Cedars-Sinai Medical Center), Håkan Olsson(Lund University), Martin Gore(Royal Marsden NHS Foundation Trust), Javier Benı́tez(Spanish National Cancer Research Centre), María J. García(Spanish National Cancer Research Centre), Irene L. Andrulis(Lunenfeld-Tanenbaum Research Institute), Anna Marie Mulligan(University Health Network), Gord Glendon(University Health Network), Ignacio Blanco(Institut Català d'Oncologia), Conxi Lázaro(Institut Català d'Oncologia), Alice S. Whittemore(Stanford Health Care), Valerie McGuire(Stanford Health Care), Weiva Sieh(Stanford Health Care), Marco Montagna(Istituto Oncologico Veneto), Elisa Alducci(Istituto Oncologico Veneto), Siegal Sadetzki(Sheba Medical Center), Angela Chetrit(Sheba Medical Center), Ava Kwong(International Hereditary Cancer Center), Susanne K. Kjær(Danish Cancer Society), Allan Jensen(Danish Cancer Society), Estrid Høgdall(Herlev Hospital), Susan L. Neuhausen(City of Hope), Robert L. Nussbaum(Cancer Research Institute), Mary B. Daly(Fox Chase Cancer Center), Mark H. Greene(National Cancer Institute), Phuong L. Mai(National Cancer Institute), Jennifer T. Loud(National Cancer Institute), Kirsten Moysich(Roswell Park Comprehensive Cancer Center), Amanda E. Toland(The Ohio State University), Diether Lambrechts(VIB-KU Leuven Center for Microbiology), Steve Ellis(Cancer Research UK Cambridge Center), Debra Frost(Cancer Research UK Cambridge Center), James D. Brenton(University of Cambridge), Marc Tischkowitz(University of Cambridge), Douglas F. Easton(Cancer Research UK Cambridge Center), Antonis C. Antoniou(Cancer Research UK Cambridge Center), Georgia Chenevix‐Trench(QIMR Berghofer Medical Research Institute), Simon A. Gayther(University of Southern California), David D.L. Bowtell(Peter MacCallum Cancer Centre), Paul D.P. Pharoah(Cancer Research UK Cambridge Center)
Clinical Cancer Research
November 15, 2014
Cited by 160Open Access
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Abstract

PURPOSE: To analyze the effect of germline mutations in BRCA1 and BRCA2 on mortality in patients with ovarian cancer up to 10 years after diagnosis. EXPERIMENTAL DESIGN: We used unpublished survival time data for 2,242 patients from two case-control studies and extended survival time data for 4,314 patients from previously reported studies. All participants had been screened for deleterious germline mutations in BRCA1 and BRCA2. Survival time was analyzed for the combined data using Cox proportional hazard models with BRCA1 and BRCA2 as time-varying covariates. Competing risks were analyzed using Fine and Gray model. RESULTS: The combined 10-year overall survival rate was 30% [95% confidence interval (CI), 28%-31%] for non-carriers, 25% (95% CI, 22%-28%) for BRCA1 carriers, and 35% (95% CI, 30%-41%) for BRCA2 carriers. The HR for BRCA1 was 0.53 at time zero and increased over time becoming greater than one at 4.8 years. For BRCA2, the HR was 0.42 at time zero and increased over time (predicted to become greater than 1 at 10.5 years). The results were similar when restricted to 3,202 patients with high-grade serous tumors and to ovarian cancer-specific mortality. CONCLUSIONS: BRCA1/2 mutations are associated with better short-term survival, but this advantage decreases over time and in BRCA1 carriers is eventually reversed. This may have important implications for therapy of both primary and relapsed disease and for analysis of long-term survival in clinical trials of new agents, particularly those that are effective in BRCA1/2 mutation carriers.


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