Patricia G. Moorman, Laura J. Havrilesky, Jennifer M. Gierisch, Remy R. Coeytaux, William J. Lowery, Vic Hasselblad, and Evan R. Myers, Duke University School of Medicine; Laura J. Havrilesky, Duke Cancer Institute, Duke University Health System; Jennifer M. Gierisch, Center for Health Services Research in Primary Care, Durham Veterans Affairs Medical Center; Jennifer M. Gierisch, Remy R. Coeytaux, Michaela Dinan, Amanda J. McBroom, and Gillian D. Sanders, Duke Clinical Research Institute, Durham; and Rachel Peragallo Urrutia, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC.
J Clin Oncol. 2013 Nov 20;31(33):4188-98. doi: 10.1200/JCO.2013.48.9021. Epub 2013 Oct 21.
To estimate the risks of ovarian cancer and breast cancer associated with oral contraceptive (OC) use among women at elevated risk owing to mutations in BRCA1/2 or a strong family history.
We searched PubMed, Embase, the Cochrane Database of Systematic Reviews, and ClinicalTrials.gov for studies published 2000 to 2012 that evaluated associations between OC use and breast or ovarian cancer among women who are carriers of a BRCA1/2 mutation or have a family history of breast or ovarian cancer.
From 6,476 unique citations, we identified six studies examining ovarian cancer risk in BRCA1/2 mutation carriers and eight studies examining breast cancer risk in BRCA1/2 mutation carriers. For BRCA1/2 mutation carriers combined, meta-analysis showed an inverse association between OC use and ovarian cancer (odds ratio [OR], 0.58; 95% CI, 0.46 to 0.73) and a nonstatistically significant association with breast cancer (OR, 1.21; 95% CI, 0.93 to 1.58). Findings were similar when examining BRCA1 and BRCA2 mutation carriers separately. Data were inadequate to perform meta-analyses examining duration or timing of use. For women with a family history of ovarian or breast cancer, we identified four studies examining risk for ovarian cancer and three for breast cancer, but differences between studies precluded combining the data for meta-analyses, and no overall pattern could be discerned.
Our analyses suggest that associations between ever use of OCs and ovarian and breast cancer among women who are BRCA1 or BRCA2 mutation carriers are similar to those reported for the general population.
评估因 BRCA1/2 突变或强烈家族史而处于高风险的女性使用口服避孕药(OC)与卵巢癌和乳腺癌风险之间的关系。
我们检索了 PubMed、Embase、Cochrane 系统评价数据库和 ClinicalTrials.gov,以评估 2000 年至 2012 年期间发表的研究,这些研究评估了携带 BRCA1/2 突变或有乳腺癌或卵巢癌家族史的女性中 OC 使用与乳腺癌或卵巢癌之间的关联。
从 6476 篇独特的参考文献中,我们确定了 6 项研究,评估了 BRCA1/2 突变携带者中卵巢癌风险,以及 8 项研究评估了 BRCA1/2 突变携带者中乳腺癌风险。综合 BRCA1/2 突变携带者的研究结果,荟萃分析显示 OC 使用与卵巢癌之间呈负相关(比值比 [OR],0.58;95%CI,0.46 至 0.73),与乳腺癌之间的相关性无统计学意义(OR,1.21;95%CI,0.93 至 1.58)。分别检查 BRCA1 和 BRCA2 突变携带者时,结果相似。数据不足,无法进行关于使用时间或持续时间的荟萃分析。对于有卵巢癌或乳腺癌家族史的女性,我们确定了 4 项研究评估卵巢癌风险,3 项研究评估乳腺癌风险,但研究之间存在差异,无法进行荟萃分析数据合并,也无法得出总体模式。
我们的分析表明,BRCA1 或 BRCA2 突变携带者中 OC 使用与卵巢癌和乳腺癌之间的关联与一般人群报告的相似。