Department of Community Medicine, University of Tromsø, Tromsø, Norway.
Int J Cancer. 2011 Jan 1;128(1):144-56. doi: 10.1002/ijc.25314.
Menopausal hormone therapy (MHT) is characterized by use of different constituents, regimens and routes of administration. We investigated the association between the use of different types of MHT and breast cancer risk in the EPIC cohort study. The analysis is based on data from 133,744 postmenopausal women. Approximately 133,744 postmenopausal women contributed to this analysis. Information on MHT was derived from country-specific self-administered questionnaires with a single baseline assessment. Incident breast cancers were identified through population cancer registries or by active follow-up (mean: 8.6 yr). Overall relative risks (RR) and 95% confidence interval (CI) were derived from country-specific Cox proportional hazard models estimates. A total of 4312 primary breast cancers were diagnosed during 1,153,747 person-years of follow-up. Compared with MHT never users, breast cancer risk was higher among current users of estrogen only (RR: 1.42, 95% CI 1.23-1.64) and higher still among current users of combined MHT (RR: 1.77, 95% CI 1.40-2.24; p = 0.02 for combined vs. estrogen-only). Continuous combined regimens conferred a 43% (95% CI: 19-72%) greater risk compared with sequential regimens. There was no significant difference between progesterone and testosterone derivatives in sequential regimens. There was no significant variation in risk linked to the estrogenic component of MHT, neither for oral vs. cutaneous administration nor for estradiol compounds vs. conjugated equine estrogens. Estrogen-only and combined MHT uses were associated with increased breast cancer risk. Continuous combined preparations were associated with the highest risk. Further studies are needed to disentangle the effects of the regimen and the progestin component.
绝经激素治疗(MHT)的特点是使用不同的成分、方案和给药途径。我们在 EPIC 队列研究中调查了不同类型的 MHT 使用与乳腺癌风险之间的关联。该分析基于 133744 名绝经后妇女的数据。大约有 133744 名绝经后妇女参与了这项分析。MHT 信息来自具有单一基线评估的特定国家的自我管理问卷。通过人群癌症登记处或主动随访(平均:8.6 年)确定新发乳腺癌病例。总体相对风险(RR)和 95%置信区间(CI)来自特定国家的 Cox 比例风险模型估计。在 1153747 人年的随访期间,共诊断出 4312 例原发性乳腺癌。与从未使用过 MHT 的女性相比,目前仅使用雌激素的女性乳腺癌风险更高(RR:1.42,95%CI 1.23-1.64),而目前联合使用 MHT 的女性乳腺癌风险更高(RR:1.77,95%CI 1.40-2.24;联合 vs. 仅雌激素,p=0.02)。与序贯方案相比,连续联合方案的风险增加了 43%(95%CI:19-72%)。在序贯方案中,孕激素和睾酮衍生物之间的风险差异无统计学意义。MHT 的雌激素成分无论是口服给药还是皮肤给药,或是雌二醇化合物与结合马雌激素相比,与风险之间均无显著差异。仅使用雌激素和联合 MHT 与乳腺癌风险增加相关。连续联合制剂与最高风险相关。需要进一步的研究来阐明方案和孕激素成分的作用。