Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20852, USA.
Cancer Causes Control. 2012 Mar;23(3):487-96. doi: 10.1007/s10552-012-9904-2. Epub 2012 Feb 25.
Previous studies have reported that lung cancer risk may be decreased, increased, or unaffected by prior use of menopausal hormone therapy (MHT).
To assess this issue further, we examined relationships among 118,008 women, ages 50-71 years who were recruited during 1995-1996 for the NIH-AARP Diet and Health Study and in whom 2,097 incident lung carcinomas were identified during follow-up through 2006. Multivariable Cox proportional hazards models estimated relative risks (RR) and 95% confidence intervals (CIs) associated with various measures of self-reported MHT use.
We found no evidence that either estrogen therapy (ET)-only or estrogen plus progestin therapy (EPT) use was substantially related to subsequent lung cancer risk (respective RRs and 95% CIs for ever use = 0.97, 0.86-1.09 and 1.03, 0.90-1.17). There were no significant variations according to currency or duration of use of either formulation, nor was there evidence that risks varied within subgroups defined by cigarette smoking or body size. The absence of effect was seen for nearly all lung cancer subtypes, with the exception of an increased risk of undifferentiated/large cell cancers associated with long-term ET-only use (p (trend) = 0.02), a relationship not observed among EPT users.
Our results failed to support any substantial alterations in lung cancer risk associated with use of either unopposed estrogen or estrogen plus progestin MHT, even when detailed exposure measures and other risk predictors were considered.
先前的研究报告称,绝经后激素治疗(MHT)的既往使用可能会降低、增加或不影响肺癌风险。
为了进一步评估这个问题,我们研究了 1995-1996 年期间招募的年龄在 50-71 岁的 118008 名女性,这些女性参加了 NIH-AARP 饮食与健康研究,在随访期间(截至 2006 年)共发现了 2097 例肺癌新发病例。多变量 Cox 比例风险模型估计了与各种自我报告的 MHT 使用相关的相对风险(RR)和 95%置信区间(CI)。
我们没有发现雌激素治疗(ET)或雌激素加孕激素治疗(EPT)的使用与随后的肺癌风险有实质性关联的证据(分别为 RR 和 95%CI 为 0.97,0.86-1.09 和 1.03,0.90-1.17)。两种制剂的使用货币或持续时间均无显著差异,也没有证据表明风险在按吸烟或体型定义的亚组中有所不同。除了长期单独使用 ET 与未分化/大细胞癌风险增加有关外(p(趋势)=0.02),几乎所有肺癌亚型的风险都没有变化,而在 EPT 使用者中没有观察到这种关系。
即使考虑了详细的暴露测量和其他风险预测因素,我们的结果也未能支持与使用未加用孕激素的雌激素或雌激素加孕激素 MHT 相关的肺癌风险有任何实质性改变。