Princess Margaret Hospital, University Health, Toronto, Canada.
J Clin Oncol. 2013 Sep 1;31(25):3069-75. doi: 10.1200/JCO.2012.46.7043. Epub 2013 Aug 5.
To evaluate the association between cumulative duration of metformin use after prostate cancer (PC) diagnosis and all-cause and PC-specific mortality among patients with diabetes.
We used a population-based retrospective cohort design. Data were obtained from several Ontario health care administrative databases. Within a cohort of men older than age 66 years with incident diabetes who subsequently developed PC, we examined the effect of duration of antidiabetic medication exposure after PC diagnosis on all-cause and PC-specific mortality. Crude and adjusted hazard ratios (HRs) were calculated by using a time-varying Cox proportional hazard model to estimate effects.
The cohort consisted of 3,837 patients. Median age at diagnosis of PC was 75 years (interquartile range [IQR], 72 to 79 years). During a median follow-up of 4.64 years (IQR, 2.7 to 7.1 years), 1,343 (35%) died, and 291 patients (7.6%) died as a result of PC. Cumulative duration of metformin treatment after PC diagnosis was associated with a significant decreased risk of PC-specific and all-cause mortality in a dose-dependent fashion. Adjusted HR for PC-specific mortality was 0.76 (95% CI, 0.64 to 0.89) for each additional 6 months of metformin use. The association with all-cause mortality was also significant but declined over time from an HR of 0.76 in the first 6 months to 0.93 between 24 and 30 months. There was no relationship between cumulative use of other antidiabetic drugs and either outcome.
Increased cumulative duration of metformin exposure after PC diagnosis was associated with decreases in both all-cause and PC-specific mortality among diabetic men.
评估前列腺癌 (PC) 诊断后二甲双胍使用累计时间与糖尿病患者全因和 PC 特异性死亡率之间的关联。
我们使用了基于人群的回顾性队列设计。数据来自安大略省几个医疗保健管理数据库。在一个年龄大于 66 岁的患有糖尿病且随后发生 PC 的男性队列中,我们研究了 PC 诊断后抗糖尿病药物暴露持续时间对全因和 PC 特异性死亡率的影响。使用时变 Cox 比例风险模型计算粗和调整后的危害比 (HR) 来估计效果。
该队列包括 3837 名患者。PC 诊断时的中位年龄为 75 岁(四分位距 [IQR],72 至 79 岁)。在中位随访 4.64 年(IQR,2.7 至 7.1 年)期间,1343 名(35%)患者死亡,291 名(7.6%)患者死于 PC。PC 诊断后二甲双胍治疗的累计时间与 PC 特异性和全因死亡率呈剂量依赖性降低风险相关。调整后的 PC 特异性死亡率 HR 为每增加 6 个月的二甲双胍使用量减少 0.76(95%CI,0.64 至 0.89)。与全因死亡率的关联也具有统计学意义,但随着时间的推移而下降,从最初 6 个月的 HR 0.76 下降到 24 至 30 个月的 0.93。其他抗糖尿病药物的累积使用与任何结局均无关系。
PC 诊断后二甲双胍暴露累计时间的增加与糖尿病男性全因和 PC 特异性死亡率的降低相关。