4.7 Article

Effects of BRCA1- and BRCA2-Related Mutations on Ovarian and Breast Cancer Survival: A Meta-analysis

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CLINICAL CANCER RESEARCH
卷 21, 期 1, 页码 211-220

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-14-1816

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  1. NIH [P50-CA83638, R01-CA142776]
  2. Department of Defense [W81XWH-10-1-0082]
  3. Ovarian Cancer Research Fund
  4. Basser Research Center for BRCA grant
  5. Marsha Rivkin Center for Ovarian Cancer Research grant
  6. Sichuan University
  7. National Natural Science Foundation of China [0040215401068]
  8. NATIONAL CANCER INSTITUTE [R01CA142776, P50CA083638, P30CA016520] Funding Source: NIH RePORTER

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Purpose: To estimate the effects of BRCA1 and BRCA2 mutations on ovarian cancer and breast cancer survival. Experimental Design: We searched PubMed and EMBASE for studies that evaluated the associations between BRCA mutations and ovarian or breast cancer survival. Meta-analysis was conducted to generate combined HRs with 95% confidence intervals (CI) for overall survival (OS) and progression-free survival (PFS). Results: From 1,201 unique citations, we identified 27 articles that compared prognosis between BRCA mutation carriers and noncarriers in patients with ovarian or breast cancer. Fourteen studies examined ovarian cancer survival and 13 studies examined breast cancer survival. For ovarian cancer, meta-analysis demonstrated that both BRCA1 and BRCA2 mutation carriers had better OS (HR, 0.76; 95% CI, 0.70-0.83 for BRCA1 mutation carriers; HR, 0.58; 95% CI, 0.50-0.66 for BRCA2 mutation carriers) and PFS (HR, 0.65; 95% CI, 0.52-0.81 for BRCA1 mutation carriers; HR, 0.61; 95% CI, 0.47-0.80 for BRCA2 mutation carriers) than noncarriers, regardless of tumor stage, grade, or histologic subtype. Among patients with breast cancer, BRCA1 mutation carriers had worse OS(HR, 1.50; 95% CI, 1.11-2.04) than noncarriers but were not significantly different from noncarriers in PFS. BRCA2 mutation was not associated with breast cancer prognosis. Conclusions: Our analyses suggest that BRCA mutations are robust predictors of outcomes in both ovarian and breast cancers and these mutations should be taken into account when devising appropriate therapeutic strategies. (C) 2014 AACR.

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