Aspirin use after diagnosis but not prediagnosis improves established colorectal cancer survival: a meta-analysis
Aspirin use after diagnosis but not prediagnosis improves established colorectal cancer survival: a meta-analysis
复制标题
诊断后使用阿司匹林而不是诊断前使用阿司匹林可以改善已确定的结直肠癌生存率:一项荟萃分析。
DOI:
10.1136/gutjnl-2014-308260
复制
发表时间:
2015-09-01
期刊:
影响因子:
24.5
通讯作者:
Wu, Yihua
中科院分区:
文献类型:
--
作者:
Li, Peiwei;Wu, Han;Wu, Yihua
Objective The objective of this meta-analysis was to systematically assess the survival benefit of aspirin use before or after diagnosis for patients with colorectal cancer (CRC).Design Relevant studies were identified through searching PubMed, Embase and Cochrane databases before May 2014. Two investigators extracted data independently for baseline characteristics and outcomes from the included studies. Either a fixed-effects or a random-effects model was derived to composite the pooled HR for overall mortality and CRC-specific mortality of CRC.Results Seven studies on postdiagnosis aspirin therapy and seven studies on prediagnosis aspirin use were finally included in this meta-analysis. The overall survival benefit associated with postdiagnosis aspirin use represented an HR of 0.84 (95% CI 0.75 to 0.94). This effect was observed both in colon cancer (HR = 0.78, 95% CI 0.64 to 0.96) and in rectal cancer (HR = 0.90, 95% CI 0.83 to 0.98). Besides, the survival benefit of postdiagnosis aspirin use appeared to be confined to those patients with positive prostaglandin endoperoxide synthase 2 (PTGS2, also known as cyclooxygenase-2, COX-2) expression (HR = 0.65, 95% CI 0.50 to 0.85) and with mutated PIK3CA tumours (HR = 0.58, 95% CI 0.37 to 0.90). Aspirin use postdiagnosis was not associated with CRC-specific mortality (HR = 0.77, 95% CI 0.52 to 1.14). We observed no evidence of an association between prediagnosis aspirin use and CRC overall mortality (HR = 1.01, 95% CI 0.96 to 1.06) or CRC-specific mortality (HR = 0.93, 95% CI 0.82 to 1.05).Conclusions These findings provide further indication that postdiagnosis aspirin therapy improved CRC overall survival, especially for patients with positive PTGS2 (COX-2) expression and mutated PIK3CA tumours.