Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Harlyne J Norris Cancer Research Tower, 1450 Biggy Street, Los Angeles, CA, 90033, USA.
Breast Cancer Res Treat. 2010 Feb;120(1):175-83. doi: 10.1007/s10549-009-0455-5. Epub 2009 Jul 14.
The potential effects of oral contraceptive (OC) and postmenopausal hormone (PMH) use are not well understood among BRCA1 or BRCA2 (BRCA1/2) deleterious mutation carriers with a history of breast cancer. We investigated the association between OC and PMH use and risk of contralateral breast cancer (CBC) in the WECARE (Women's Environment, Cancer, and Radiation Epidemiology) Study. The WECARE Study is a population-based case-control study of 705 women with asynchronous CBC and 1,398 women with unilateral breast cancer, including 181 BRCA1/2 mutation carriers. Risk-factor information was assessed by telephone interview. Mutation status was measured using denaturing high-performance liquid chromatography followed by direct sequencing in all participants. Outcomes, treatment, and tumor characteristics were abstracted from medical records. Ever use of OCs was not associated with risk among noncarriers (RR = 0.87; 95% CI = 0.66-1.15) or BRCA2 carriers (RR = 0.82; 95% CI = 0.21-3.13). BRCA1 carriers who used OCs had a nonsignificant greater risk than nonusers (RR = 2.38; 95% CI = 0.72-7.83). Total duration of OC use and at least 5 years of use before age 30 were associated with a nonsignificant increased risk among mutation carriers but not among noncarriers. Few women had ever used PMH and we found no significant associations between lifetime use and CBC risk among carriers and noncarriers. In conclusion, the association between OC/PMH use and risk of CBC does not differ significantly between carriers and noncarriers; however, because carriers have a higher baseline risk of second primaries, even a potential small increase in risk as a result of OC use may be clinically relevant.
口服避孕药 (OC) 和绝经后激素 (PMH) 在有乳腺癌病史的 BRCA1 或 BRCA2 (BRCA1/2) 有害突变携带者中的潜在影响尚不清楚。我们研究了 OC 和 PMH 使用与 WECARE(妇女环境、癌症和辐射流行病学)研究中对侧乳腺癌 (CBC) 风险之间的关联。WECARE 研究是一项基于人群的病例对照研究,纳入了 705 例对侧 CBC 女性和 1398 例单侧乳腺癌女性,包括 181 例 BRCA1/2 突变携带者。通过电话访谈评估风险因素信息。在所有参与者中,使用变性高效液相色谱法 (DHPLC) 结合直接测序来测量突变状态。结局、治疗和肿瘤特征从病历中提取。从未使用过 OC 的非携带者 (RR = 0.87; 95%CI = 0.66-1.15) 或 BRCA2 携带者 (RR = 0.82; 95%CI = 0.21-3.13) 中,OC 使用与风险无关。与非使用者相比,OC 使用者的 BRCA1 携带者风险有增加的趋势,但无统计学意义 (RR = 2.38; 95%CI = 0.72-7.83)。OC 使用的总时长和 30 岁之前至少使用 5 年与突变携带者而非非携带者的风险增加无显著关联。很少有女性曾使用过 PMH,我们未发现携带者和非携带者终生使用 PMH 与 CBC 风险之间存在显著关联。总之,OC/PMH 使用与 CBC 风险之间的关联在携带者和非携带者之间无显著差异;然而,由于携带者的二次原发性疾病的基线风险较高,因此 OC 使用导致的潜在风险增加可能具有临床意义。