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A case–control analysis of oral contraceptive use and breast cancer subtypes in the African American Breast Cancer Epidemiology and Risk Consortium

机译:非裔美国人乳腺癌流行病学和风险协会对口服避孕药使用和乳腺癌亚型的病例对照分析

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IntroductionRecent oral contraceptive (OC) use has been consistently associated with increased risk of breast cancer, but evidence on specific breast cancer subtypes is sparse.MethodsWe investigated recency and duration of OC use in relation to molecular subtypes of breast cancer in a pooled analysis of data from the African American Breast Cancer Epidemiology and Risk Consortium. The study included 1,848 women with estrogen receptor-positive (ER+) breast cancer, 1,043 with ER-negative (ER-) breast cancer (including 494 triple negative (TN) tumors, which do not have receptors for estrogen, progesterone, and human epidermal growth factor 2), and 10,044 controls. Multivariable polytomous logistic regression models were used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for exposure categories relative to never use, controlling for potential confounding variables.ResultsOC use within the previous 5?years was associated with increased risk of ER+ (OR 1.46, 95% CI 1.18 to 1.81), ER- (OR 1.57, 95% CI 1.22 to 1.43), and TN (OR 1.78, 95% CI 1.25 to 2.53) breast cancer. The risk declined after cessation of use but was apparent for ER+ cancer for 15 to 19?years after cessation and for ER- breast cancer for an even longer interval after cessation. Long duration of use was also associated with increased risk of each subtype, particularly ER-.ConclusionsOur results suggest that OC use, particularly recent use of long duration, is associated with an increased risk of ER+, ER-, and TN breast cancer in African American women. Research into mechanisms that explain these findings, especially the association with ER- breast cancer, is needed.
机译:前言最近口服避孕药(OC)一直与乳腺癌风险增加有关,但有关特定乳腺癌亚型的证据很少。方法我们在汇总数据分析中调查了与乳腺癌分子亚型相关的OC近期使用和持续时间来自非裔美国人乳腺癌流行病学和风险协会。该研究包括1,848名患有雌激素受体阳性(ER +)乳腺癌的妇女,1,043名患有ER阴性(ER-)乳腺癌(包括494例三阴性(TN)肿瘤)的妇女,这些肿瘤没有雌激素,孕激素和人类表皮受体生长因子2)和10044个对照。多变量多因素logistic回归模型用于估计暴露类别相对于从未使用的比值比(OR)和95%置信区间(CI),以控制潜在的混杂变量。结果在过去5年内使用OC与患病风险增加相关ER +(OR 1.46,95%CI 1.18至1.81),ER-(OR 1.57,95%CI 1.22至1.43)和TN(OR 1.78,95%CI 1.25至2.53)乳腺癌。停止使用后风险降低,但在停止使用ER +癌症后15到19年明显,而停止使用ER-乳腺癌的风险甚至更长。结论长时间使用还与每种亚型,特别是ER-的风险增加相关。结论我们的结果表明,在非洲,OC的使用,尤其是近期的长期使用,与ER +,ER-和TN乳腺癌风险增加相关美国妇女。需要研究解释这些发现的机制,尤其是与ER-乳腺癌的关系。

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