Bradley Marie C, Black Amanda, Freedman Andrew N, Barron Thomas I
Clinical and Translational Epidemiology Branch, Epidemiology and Genomics Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, Maryland.
Epidemiology and Biostatistics Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
Cancer. 2016 Jul 1;122(13):2067-75. doi: 10.1002/cncr.30004. Epub 2016 May 3.
There is a body of evidence indicating that aspirin may reduce the risk of cancer mortality. However, to the authors' knowledge, the optimal exposure timing and mechanism of action remain unclear. In the current study, the authors investigated associations between prediagnostic aspirin use and breast cancer-specific mortality in a US population.
Postmenopausal women diagnosed with stage I to III breast cancer (1993-2009) were identified (2925 women with a total of 18,073 person-years) from the National Cancer Institute's Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial. Prediagnostic aspirin use (1274 women) was identified from study questionnaires. Multivariate Cox proportional hazards models were used to estimate hazard ratios (HRs) with 95% confidence intervals (95% CIs) for associations between aspirin use and breast cancer-specific mortality. Effect modification by lymph node status was evaluated.
Prediagnostic aspirin use was not found to be associated with lower breast cancer-specific mortality (HR, 0.95; 95% CI, 0.68-1.31 [P = .74]). In analyses stratified by lymph node status, aspirin use was found to be associated with lower breast cancer-specific mortality among women with lymph node-negative tumors (HR, 0.54; 95% CI, 0.32-0.93 [P = 0.02]), but not those with lymph node-positive tumors (HR, 1.41; 95% CI, 0.92-2.16 [P = 0.11]). Tests for interaction were found to be statistically significant (P for interaction =.006). No association was noted between aspirin use and lymph node status.
Prediagnostic aspirin use was not found to be associated with a reduction in breast cancer-specific mortality overall. However, effect modification by lymph node status was observed and mortality was found to be reduced by approximately one-half among aspirin users with lymph node-negative disease. This represents a clinically significant reduction in breast cancer mortality. These findings contribute to the understanding of aspirin's mechanism of action in breast cancer. However, further etiologic research to understand this association is warranted. Cancer 2016;122:2067-75. © 2016 American Cancer Society.
有大量证据表明阿司匹林可能降低癌症死亡率。然而,据作者所知,最佳暴露时间和作用机制仍不清楚。在当前研究中,作者调查了美国人群中癌症诊断前使用阿司匹林与乳腺癌特异性死亡率之间的关联。
从美国国立癌症研究所的前列腺、肺、结直肠癌和卵巢癌筛查试验中确定了1993年至2009年诊断为I至III期乳腺癌的绝经后女性(2925名女性,共18073人年)。通过研究问卷确定癌症诊断前使用阿司匹林的情况(1274名女性)。使用多变量Cox比例风险模型估计阿司匹林使用与乳腺癌特异性死亡率之间关联的风险比(HR)及其95%置信区间(95%CI)。评估了淋巴结状态的效应修正。
未发现癌症诊断前使用阿司匹林与降低乳腺癌特异性死亡率相关(HR,0.95;95%CI,0.68 - 1.31 [P = 0.74])。在按淋巴结状态分层的分析中,发现阿司匹林使用与淋巴结阴性肿瘤女性的乳腺癌特异性死亡率降低相关(HR,0.54;95%CI,0.32 - 0.93 [P = 0.02]),但与淋巴结阳性肿瘤女性无关(HR,1.41;95%CI,0.92 - 2.16 [P = 0.11])。发现交互作用检验具有统计学意义(交互作用P值 = 0.006)。未发现阿司匹林使用与淋巴结状态之间存在关联。
总体而言,未发现癌症诊断前使用阿司匹林与降低乳腺癌特异性死亡率相关。然而,观察到了淋巴结状态的效应修正,并且发现淋巴结阴性疾病的阿司匹林使用者死亡率降低了约一半。这代表了乳腺癌死亡率在临床上的显著降低。这些发现有助于理解阿司匹林在乳腺癌中的作用机制。然而,有必要进行进一步的病因学研究以了解这种关联。《癌症》2016年;122:2067 - 75。© 2016美国癌症协会