Bethea Traci N, Rosenberg Lynn, Hong Chi-Chen, Troester Melissa A, Lunetta Kathryn L, Bandera Elisa V, Schedin Pepper, Kolonel Laurence N, Olshan Andrew F, Ambrosone Christine B, Palmer Julie R
Breast Cancer Res. 2015 Feb 21;17(1):22. doi: 10.1186/s13058-015-0535-x.
Recent oral contraceptive (OC) use has been consistently associated with increased risk of breast cancer, but evidence on specific breast cancer subtypes is sparse.
We 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.
OC 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-.
Our 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.
近期使用口服避孕药(OC)一直与乳腺癌风险增加相关,但关于特定乳腺癌亚型的证据却很稀少。
我们在对非裔美国乳腺癌流行病学与风险联盟的数据进行汇总分析时,研究了OC使用的近期情况和持续时间与乳腺癌分子亚型之间的关系。该研究纳入了1848例雌激素受体阳性(ER+)乳腺癌女性、1043例雌激素受体阴性(ER-)乳腺癌女性(包括494例三阴性(TN)肿瘤,即不具有雌激素、孕激素和人表皮生长因子2受体)以及10044例对照。使用多变量多分类逻辑回归模型来估计相对于从未使用者,暴露类别对应的比值比(OR)和95%置信区间(CI),同时控制潜在的混杂变量。
过去5年内使用OC与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)乳腺癌风险增加相关。停用后风险降低,但停用后15至19年ER+癌风险仍明显,ER-乳腺癌风险在停用后更长时间内仍明显。长期使用也与各亚型风险增加相关,尤其是ER-。
我们的结果表明,使用OC,尤其是近期长期使用,与非裔美国女性ER+、ER-和TN乳腺癌风险增加相关。需要对解释这些发现的机制进行研究,尤其是与ER-乳腺癌的关联。