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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Metformin use and survival after colorectal cancer: A population-based cohort study
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Metformin use and survival after colorectal cancer: A population-based cohort study

机译:大肠癌术后二甲双胍的使用和生存:一项基于人群的队列研究

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Preclinical evidence suggests that metformin could delay cancer progression. Previous epidemiological studies however have been limited by small sample sizes and certain time-related biases. This study aimed to investigate whether colorectal cancer patients with type 2 diabetes who were exposed to metformin had reduced cancer-specific mortality. We conducted a retrospective cohort study of 1,197 colorectal cancer patients newly diagnosed from 1998 to 2009 (identified from English cancer registries) with type 2 diabetes (based upon Clinical Practice Research Datalink, CPRD, prescription and diagnosis records). In this cohort 382 colorectal cancer-specific deaths occurred up to 2012 from the Office of National Statistics (ONS) mortality data. Metformin use was identified from CPRD prescription records. Using time-dependent Cox regression models, unadjusted and adjusted hazard ratios (HR) and 95% CIs were calculated for the association between post-diagnostic exposure to metformin and colorectal cancer-specific mortality. Overall, there was no evidence of an association between metformin use and cancer-specific death before or after adjustment for potential confounders (adjusted HR 1.06, 95% CI 0.80, 1.40). In addition, after adjustment for confounders, there was also no evidence of associations between other diabetic medications and cancer-specific mortality including sulfonylureas (HR 1.14, 95% CI 0.86, 1.51), insulin use (HR 1.35, 95% CI 0.95, 1.93) or other antidiabetic medications including thiazolidinediones (HR 0.73, 95% CI 0.46, 1.14). Similar associations were observed by duration of use and for all-cause mortality. This population-based study, the largest to date, does not support a protective association between metformin and survival in colorectal cancer patients.
机译:临床前证据表明二甲双胍可以延缓癌症的进展。但是,以前的流行病学研究受到样本量少和某些与时间有关的偏倚的限制。这项研究旨在调查暴露于二甲双胍的2型糖尿病大肠癌患者是否降低了癌症特异性死亡率。我们进行了一项回顾性队列研究,研究对象是1998年至2009年新诊断为2型糖尿病的1,197例结直肠癌患者(根据临床实践研究数据链,CPRD,处方和诊断记录)。截至2012年,根据国家统计局(ONS)的死亡率数据,共发生382例大肠癌特异性死亡。从CPRD处方记录中确定了二甲双胍的使用。使用时间依赖的Cox回归模型,计算出未调整和调整后的危险比(HR)和95%CI,用于诊断后二甲双胍暴露与大肠癌特异性死亡率之间的关系。总体而言,在调整潜在混杂因素之前或之后,没有证据表明二甲双胍的使用与癌症特异性死亡之间存在关联(校正后的HR 1.06、95%CI 0.80、1.40)。此外,在对混杂因素进行调整后,也没有证据表明其他糖尿病药物与癌症特异性死亡率之间存在关联,包括磺脲类药物(HR 1.14,95%CI 0.86,1.51),胰岛素使用(HR 1.35,95%CI 0.95,1.93)。 )或其他抗糖尿病药物,包括噻唑烷二酮(HR 0.73,95%CI 0.46,1.14)。使用期限和全因死亡率观察到相似的关联。这项基于人群的研究是迄今为止最大的一项研究,不支持二甲双胍与大肠癌患者生存之间的保护性关联。

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