Aspirin use after diagnosis but not prediagnosis improves established colorectal cancer survival: a meta-analysis

阿司匹林 医学 结直肠癌 内科学 荟萃分析 胃肠病学 比例危险模型 癌症 肿瘤科 外科
作者
Peiwei Li,Han Wu,Honghe Zhang,Yu Shi,Jinming Xu,Yao Ye,Dajing Xia,Jun Yang,Jianting Cai,Yihua Wu
出处
期刊:Gut [BMJ]
卷期号:64 (9): 1419-1425 被引量:143
标识
DOI:10.1136/gutjnl-2014-308260
摘要

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).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.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).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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ada阿达完成签到,获得积分10
6秒前
Beyond095完成签到 ,获得积分10
7秒前
蛋卷完成签到 ,获得积分0
7秒前
靓丽的采白完成签到,获得积分10
8秒前
大气的迎丝完成签到 ,获得积分10
12秒前
菲菲完成签到,获得积分10
13秒前
梁白开完成签到,获得积分10
15秒前
16秒前
cdercder应助科研通管家采纳,获得10
16秒前
cdercder应助科研通管家采纳,获得10
16秒前
所所应助科研通管家采纳,获得10
16秒前
cdercder应助科研通管家采纳,获得10
16秒前
cdercder应助科研通管家采纳,获得10
16秒前
lambs13完成签到,获得积分10
17秒前
yoooooooo完成签到,获得积分10
18秒前
俏皮冰露完成签到,获得积分10
18秒前
633完成签到 ,获得积分10
24秒前
vitamin完成签到 ,获得积分0
26秒前
369ninja发布了新的文献求助10
29秒前
美丽的芙完成签到 ,获得积分10
41秒前
stiger完成签到,获得积分0
44秒前
学术霸王完成签到,获得积分10
46秒前
hyl-tcm完成签到 ,获得积分10
46秒前
STEAD完成签到,获得积分10
1分钟前
Zhao完成签到 ,获得积分10
1分钟前
1分钟前
动听的又亦完成签到 ,获得积分10
1分钟前
虎鲸_thEt发布了新的文献求助10
1分钟前
wangyue1230完成签到,获得积分10
1分钟前
1分钟前
身体健康完成签到 ,获得积分10
1分钟前
共享精神应助鹿无虞采纳,获得10
1分钟前
拓小八完成签到,获得积分0
1分钟前
1分钟前
鹿无虞发布了新的文献求助10
1分钟前
怀亦完成签到 ,获得积分10
1分钟前
tmobiusx完成签到,获得积分10
1分钟前
一一完成签到,获得积分0
1分钟前
1分钟前
chen完成签到 ,获得积分10
1分钟前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Arthritis and Related Conditions, An Issue of Orthopedic Clinics 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7290557
求助须知:如何正确求助?哪些是违规求助? 8909741
关于积分的说明 18857043
捐赠科研通 6957951
什么是DOI,文献DOI怎么找? 3209151
关于科研通互助平台的介绍 2378930
邀请新用户注册赠送积分活动 2184884