Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan.
College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Int J Cancer. 2020 Oct 1;147(7):1904-1916. doi: 10.1002/ijc.32989. Epub 2020 Apr 8.
Epidemiological evidence for the association between postdiagnostic metformin use and survival in patients with colorectal cancer (CRC) remains limited. Using the Taiwan Cancer Registry database, a cohort of 16,676 diabetic patients newly diagnosed with CRC from January 1, 2004 through December 31, 2014, followed until December 31, 2016, was identified. Postdiagnostic use of metformin (two or more prescriptions after CRC diagnosis) was defined as a time-dependent covariate with 6-month lag. Multivariate Cox regression model and stabilized inverse probability of treatment weighting (IPTW) were used to estimate adjusted effects of metformin on all-cause mortality and CRC-specific mortality during follow-up. A number of 11,438 (69%) received metformin after CRC diagnosis. Overall, 7,393 deaths, including 4,845 CRC-specific deaths, were observed during 64,322 person-years of follow-up. After adjustment for demographic and clinical covariates, metformin users had lower all-cause mortality than did nonusers (hazard ratio [HR], 0.42; 95% confidence interval [CI], 0.40-0.44) and lower CRC-specific mortality (HR, 0.41; 95% CI, 0.39-0.44). Similar but somewhat attenuated effects were observed after stabilized IPTW (HR for all-cause mortality, 0.56; 95% CI, 0.53-0.59; HR for CRC-specific mortality, 0.58; 95% CI, 0.55-0.61). Similar results were observed in stratified analyses of 2,112 patients with no prediagnostic metformin use and 14,564 patients with prediagnostic metformin use. Findings for both outcomes were consistent in multiple sensitivity analyses. Use of postdiagnostic metformin was associated with significantly lower all-cause mortality and CRC-specific mortality, regardless of prior metformin use. These findings support the use of metformin as an adjunct to standard care of diabetic patients with CRC.
使用台湾癌症登记数据库,我们确定了一个队列,该队列包括 2004 年 1 月 1 日至 2014 年 12 月 31 日期间新诊断为 CRC 的 16676 名糖尿病患者,随访至 2016 年 12 月 31 日。诊断后使用二甲双胍(CRC 诊断后开了 2 个或更多处方)被定义为一个时间依赖的协变量,有 6 个月的滞后。多变量 Cox 回归模型和稳定的逆概率治疗加权(IPTW)用于估计二甲双胍在随访期间对全因死亡率和 CRC 特异性死亡率的调整效果。共有 11438 人(69%)在 CRC 诊断后接受了二甲双胍治疗。在 64322 人年的随访期间,共观察到 7393 例死亡,包括 4845 例 CRC 特异性死亡。在调整了人口统计学和临床协变量后,二甲双胍使用者的全因死亡率低于未使用者(风险比 [HR],0.42;95%置信区间 [CI],0.40-0.44),CRC 特异性死亡率也较低(HR,0.41;95% CI,0.39-0.44)。在稳定的 IPTW 后观察到类似但略有减弱的效果(全因死亡率的 HR 为 0.56;95% CI,0.53-0.59;CRC 特异性死亡率的 HR 为 0.58;95% CI,0.55-0.61)。在无预诊断二甲双胍使用的 2112 名患者和预诊断二甲双胍使用的 14564 名患者的分层分析中观察到了类似的结果。两种结果的敏感性分析结果一致。无论是否有预诊断二甲双胍使用,诊断后使用二甲双胍均与全因死亡率和 CRC 特异性死亡率显著降低相关。这些发现支持将二甲双胍作为糖尿病合并 CRC 患者标准治疗的辅助手段。