Zhou Cindy Ke, Daugherty Sarah E, Liao Linda M, Freedman Neal D, Abnet Christian C, Pfeiffer Ruth, Cook Michael B
Metabolic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, Maryland.
Clinical Effectiveness Research, Patient-Centered Outcomes Research Institute, Washington, DC.
Cancer Prev Res (Phila). 2017 Jul;10(7):410-420. doi: 10.1158/1940-6207.CAPR-17-0033. Epub 2017 May 15.
Prostate cancer is one of the leading causes of cancer-related death in U.S. men. There is an unmet need to identify modifiable risk factors for prostate cancer survival. Experimental studies have suggested that nonsteroidal anti-inflammatory drugs (NSAIDs) may improve prostate cancer survival through antithrombotic and anti-inflammation mechanisms. Results from previous observational studies have been equivocal, and few have assessed whether an etiologically relevant time window of exposure exists. We sampled incident prostate cancer cases from two large U.S. prospective cohorts, NIH-AARP Diet and Health Study and PLCO Cancer Screening Trial, to investigate whether pre- and postdiagnostic aspirin and non-aspirin NSAID use were associated with prostate cancer-specific and all-cause mortality. Cox proportional hazards regression models estimated hazard ratios (HRs) and 95% confidence intervals (CIs). Study-specific results were meta-analyzed using fixed-effects models. Pre- and postdiagnostic aspirin or non-aspirin NSAID use were not statistically significantly associated with prostate cancer-specific mortality. However, occasional (less than daily) and daily aspirin users five years or more before prostate cancer diagnosis had 18% (HR = 0.82; 95% CI = 0.75-0.90) and 15% (HR = 0.85; 95% CI = 0.77-0.94) reduced all-cause mortality versus nonusers. Similarly, postdiagnostic occasional and daily aspirin use were associated with 17% (HR = 0.83; 95% CI=0.72-0.95) and 25% (HR = 0.75; 95% CI = 0.66-0.86) reduced all-cause mortality, independent of prediagnostic aspirin use. This study suggests that aspirin or non-aspirin NSAIDs are not associated with prostate cancer survival. However, aspirin use both before and after prostate cancer diagnosis was associated with longer overall survival, highlighting the importance of comorbidity prevention among prostate cancer survivors. .
前列腺癌是美国男性癌症相关死亡的主要原因之一。目前仍存在未满足的需求,即需要确定可改变的前列腺癌生存风险因素。实验研究表明,非甾体抗炎药(NSAIDs)可能通过抗血栓形成和抗炎机制改善前列腺癌患者的生存情况。以往观察性研究的结果并不明确,而且很少有研究评估是否存在病因学上相关的暴露时间窗。我们从美国两个大型前瞻性队列研究(NIH-AARP饮食与健康研究和PLCO癌症筛查试验)中抽取前列腺癌新发病例,以调查诊断前后使用阿司匹林和非阿司匹林类NSAIDs是否与前列腺癌特异性死亡率和全因死亡率相关。Cox比例风险回归模型估计风险比(HRs)和95%置信区间(CIs)。使用固定效应模型对各研究的结果进行荟萃分析。诊断前后使用阿司匹林或非阿司匹林类NSAIDs与前列腺癌特异性死亡率无统计学显著关联。然而,在前列腺癌诊断前五年或更长时间偶尔(少于每日)和每日服用阿司匹林的患者,与未使用者相比,全因死亡率分别降低了18%(HR = 0.82;95%CI = 0.75 - 0.90)和15%(HR = 0.85;95%CI = 0.77 - 0.94)。同样,诊断后偶尔和每日服用阿司匹林与全因死亡率分别降低17%(HR = 0.83;95%CI = 0.72 - 0.95)和25%(HR = 0.75;95%CI = 0.66 - 0.86)相关,且与诊断前是否使用阿司匹林无关。这项研究表明,阿司匹林或非阿司匹林类NSAIDs与前列腺癌生存无关。然而,前列腺癌诊断前后使用阿司匹林均与更长的总生存期相关,这凸显了前列腺癌幸存者中预防合并症的重要性。