Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, PA 19104-6021, USA.
Pharmacoepidemiol Drug Saf. 2010 May;19(5):440-7. doi: 10.1002/pds.1941.
Among unanswered questions is whether menopausal use of estrogen therapy (ET) or estrogen-plus-progestin therapy (CHT) increases risk of developing fatal breast cancer i.e., developing and dying of breast cancer. Using a population-based case-control design, we estimated incidence rate ratios of fatal breast cancer in postmenopausal hormone therapy (HT) users compared to non-users by type, duration, and recency of HT use.
HT use prior to breast cancer diagnosis in 278 women who died of breast cancer within 6 years of diagnosis (cases) was compared with use in 2224 controls never diagnosed with breast cancer using conditional logistic regression. Measures taken to address potential bias and confounding inherent in case-control studies included collecting and adjusting for detailed data on demographic and other factors potentially associated both with HT use and breast cancer.
Fifty-six per cent of cases and 68% of controls reported HT use. Among current 3+ year HT users, odds ratios and 95% confidence intervals for death were 0.83 (0.50, 1.38) and 0.69 (0.44, 1.09), respectively, for exclusive use of CHT or of ET, and were 0.94 (0.59, 1.48) and 0.70 (0.45, 1.07) for any use of CHT or of ET regardless of other hormone use.
Point estimates suggest no increased risk of fatal breast cancer with HT use, although 50% increases in risk in longer-term current CHT users cannot be ruled out.
仍有未解决的问题,即绝经后使用雌激素治疗(ET)或雌孕激素联合治疗(CHT)是否会增加致命性乳腺癌的风险,即发生乳腺癌并因此死亡。本研究采用基于人群的病例对照设计,通过 HT 类型、持续时间和近期使用情况,估计了绝经后激素治疗(HT)使用者与非使用者致命性乳腺癌的发病率比。
在 278 名确诊后 6 年内死于乳腺癌的患者(病例)中,比较了其在乳腺癌诊断前使用 HT 的情况,并与从未确诊过乳腺癌的 2224 名对照者进行了比较,采用条件逻辑回归分析。为解决病例对照研究固有的潜在偏倚和混杂因素,采取了收集和调整与 HT 使用和乳腺癌均相关的详细人口统计学和其他因素数据等措施。
56%的病例和 68%的对照者报告了 HT 使用情况。在当前使用 3 年以上 HT 的人群中,仅使用 CHT 或 ET 的死亡比值比及其 95%置信区间分别为 0.83(0.50,1.38)和 0.69(0.44,1.09),而使用 CHT 或 ET 的任何情况的比值比及其 95%置信区间分别为 0.94(0.59,1.48)和 0.70(0.45,1.07)。
点估计提示 HT 使用与致命性乳腺癌风险增加无关,尽管不能排除长期当前 CHT 使用者的风险增加 50%。