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首页> 外文期刊>Journal of Cancer >Long-term aspirin use for primary cancer prevention: An updated systematic review and subgroup meta-analysis of 29 randomized clinical trials
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Long-term aspirin use for primary cancer prevention: An updated systematic review and subgroup meta-analysis of 29 randomized clinical trials

机译:用于预防原发性癌症的长期阿司匹林:29例随机临床试验的更新系统评论和亚组荟萃分析

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Background and objective: Long-term aspirin use for the primary prevention of cancer remains controversial, and variations in the effect of aspirin use on cancer outcomes by aspirin dose, follow-up duration, or study population have never been systematically evaluated. The objective of this study was to evaluate the effect of aspirin on primary cancer prevention and to determine whether the effect differed according to aspirin dose, follow-up duration, or study population. Materials and methods: Seven electronic databases were searched from inception to September 30, 2019. Randomized clinical trials (RCTs) that compared aspirin use versus no aspirin use in participants without pre-existing cancer and reported cancer outcomes were selected. Data were screened and extracted by different investigators. Analyses were performed using Review Manager 5.3 and Comprehensive Meta-Analysis 2.0. Total cancer incidence was defined as the primary clinical endpoint. Total cancer mortality, all-cause mortality, major bleeding, and total bleeding events were the secondary outcomes. Subgroup analyses were conducted based on aspirin dose, follow-up duration, and study populations. Results: Twenty-nine RCTs that randomized 200,679 participants were included. Compared with no aspirin, aspirin use was not associated with significant reductions in total cancer incidence (RR = 1.01, 95% CI: 0.97 to 1.04, P = 0.72), total cancer mortality (RR = 1.00, 95% CI: 0.93 to 1.07, P = 0.90), or all-cause mortality (RR = 0.98, 95% CI: 0.94 to 1.02, P =0.31); however, aspirin use was associated with a 44% increase in the risk of major bleeding (RR = 1.44, 95% CI: 1.32 to 1.57, P 0.00001) and a 52% increase in the risk of total bleeding events (RR = 1.52, 95% CI: 1.33 to 1.74, P 0.00001). Subgroup analyses demonstrated consistent results. Conclusions: Long-term aspirin use in individuals without pre-existing cancer was not associated with a significant reduction in total cancer incidence, cancer mortality, or all-cause mortality; however, aspirin use was associated with a significant increase in the risk of bleeding. Therefore, aspirin is not an appropriate choice for the primary cancer prevention.? The author(s).
机译:背景和目的:长期阿司匹林用于初步预防癌症的使用仍存在争议,并且从未系统地评估了阿司匹林剂量,随访期间或研究人群对癌症结果对癌症结果影响的变化。本研究的目的是评估阿司匹林对原发性癌症预防的影响,并确定效果是否根据阿司匹林剂量,随访持续时间或研究群体不同。材料和方法:从2009年9月30日开始搜查了七个电子数据库。比较阿司匹林使用与参与者在没有预先存在的癌症和报告的癌症结果的参与者中使用阿司匹林使用的随机临床试验(RCT)。数据被不同的研究人员筛选和提取。使用审查经理5.3和全面的Meta-Analysis 2.0进行分析。总癌症发病率被定义为主要临床终点。总癌症死亡率,全因死亡率,重大出血和总出血事件是二次结果。基于阿司匹林剂量,随访持续时间和研究群体进行亚组分析。结果:包括200,679名参与者随机的二十九个RCT。与无阿司匹林相比,阿司匹林使用与总癌症发病率的显着降低无关(RR = 1.01,95%CI:0.97至1.04,P = 0.72),总癌症死亡率(RR = 1.00,95%CI:0.93至1.07 ,p = 0.90),或全部原因死亡率(RR = 0.98,95%CI:0.94至1.02,P = 0.31);然而,阿司匹林使用与主要出血风险的风险增加44%(RR = 1.44,95%CI:1.32至1.57,P <0.00001),并且总出血事件的风险增加了52%(RR = 1.52 ,95%CI:1.33至1.74,P <0.00001)。子组分析显示一致的结果。结论:在没有预先存在的癌症的情况下,人们在没有预先存在的癌症的情况下使用的长期阿司匹林与总癌症发病率,癌症死亡率或全导致死亡率的显着降低无关;然而,阿司匹林使用与出血风险的显着增加有关。 Therefore, aspirin is not an appropriate choice for the primary cancer prevention.?作者。

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