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【medical-news】《柳叶刀》新研究称小剂量阿司匹

In an Article, Rothwell and colleagues examine deaths due to all cancers during and after randomised trials of daily aspirin versus control originally for prevention of vascular events. The authors study eight eligible trials which covered 25,570 patients. The findings could have implications for guidelines on use of aspirin and for understanding of carcinogenesis and its susceptibility to drug intervention.

文章如下:

Effect of daily aspirin on long-term risk of death due to cancer: analysis of individual patient data from randomised trials

链接:http://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)62110-1/fulltext

Summary

Background
Treatment with daily aspirin for 5 years or longer reduces subsequent risk of colorectal cancer. Several lines of evidence suggest that aspirin might also reduce risk of other cancers, particularly of the gastrointestinal tract, but proof in man is lacking. We studied deaths due to cancer during and after randomised trials of daily aspirin versus control done originally for prevention of vascular events.
Methods
We used individual patient data from all randomised trials of daily aspirin versus no aspirin with mean duration of scheduled trial treatment of 4 years or longer to determine the effect of allocation to aspirin on risk of cancer death in relation to scheduled duration of trial treatment for gastrointestinal and non-gastrointestinal cancers. In three large UK trials, long-term post-trial follow-up of individual patients was obtained from death certificates and cancer registries.
Results
In eight eligible trials (25 570 patients, 674 cancer deaths), allocation to aspirin reduced death due to cancer (pooled odds ratio [OR] 0·79, 95% CI 0·68—0·92, p=0·003). On analysis of individual patient data, which were available from seven trials (23 535 patients, 657 cancer deaths), benefit was apparent only after 5 years' follow-up (all cancers, hazard ratio [HR] 0·66, 0·50—0·87; gastrointestinal cancers, 0·46, 0·27—0·77; both p=0·003). The 20-year risk of cancer death (1634 deaths in 12 659 patients in three trials) remained lower in the aspirin groups than in the control groups (all solid cancers, HR 0·80, 0·72—0·88, p<0·0001; gastrointestinal cancers, 0·65, 0·54—0·78, p<0·0001), and benefit increased (interaction p=0·01) with scheduled duration of trial treatment (≥7·5 years: all solid cancers, 0·69, 0·54—0·88, p=0·003; gastrointestinal cancers, 0·41, 0·26—0·66, p=0·0001). The latent period before an effect on deaths was about 5 years for oesophageal, pancreatic, brain, and lung cancer, but was more delayed for stomach, colorectal, and prostate cancer. For lung and oesophageal cancer, benefit was confined to adenocarcinomas, and the overall effect on 20-year risk of cancer death was greatest for adenocarcinomas (HR 0·66, 0·56—0·77, p<0·0001). Benefit was unrelated to aspirin dose (75 mg upwards), sex, or smoking, but increased with age—the absolute reduction in 20-year risk of cancer death reaching 7·08% (2·42—11·74) at age 65 years and older.
Interpretation
Daily aspirin reduced deaths due to several common cancers during and after the trials. Benefit increased with duration of treatment and was consistent across the different study populations. These findings have implications for guidelines on use of aspirin and for understanding of carcinogenesis and its susceptibility to drug intervention.
Funding
None 研究:阿司匹林可降低癌症死亡率25%

英国《金融时报》 克莱夫•库克森 伦敦报道

今日发表的研究报告表明,每日服用一片阿司匹林可将癌症死亡率降低25%。

这份发表在英国医学杂志《柳叶刀》(Lancet)上、针对25570名病人的研究表明,5年来坚持每天服用小剂量阿司匹林的所有类型的癌症病人长期死亡率有所下降。

英国东英吉利大学(University of East Anglia)转化医学教授阿拉斯泰尔•沃森(Alastair Watson)表示,最新研究“进一步证明,阿司匹林是世界上遥遥领先的最神奇的药物”。

每日服用阿司匹林,使得结直肠癌死亡率降低40%,食道癌死亡率降低60%。

19世纪末,德国拜耳公司(Bayer)合成出阿司匹林并将其大规模推向市场,标志着现代药物的问世。许多专家相信,制药业的首只药物从未被超越。

由牛津大学(Oxford university)的彼得•罗斯维尔(Peter Rothwell)牵头进行的此项研究,以8项旨在评估阿司匹林在预防心血管疾病方面效用的临床实验的数据为基础,此前这被视为阿司匹林的主要效用。研究人员审议了参与者长达20年的病历,聚焦于癌症。

卡地夫大学(Cardiff University)的彼得•埃尔伍德(Peter Elwood)表示,阿司匹林对成年人的主要副作用是加大了胃岀血的风险,但这只影响2000人中的一人,小剂量服用几乎从不致命。埃尔伍德研究阿司匹林将近40年。

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作者:admin@医学,生命科学    2010-12-24 21:45
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