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基于肠降血糖素的治疗与胰腺癌的短期风险:两项回顾性队列研究的结果。

Incretin-Based Therapies and the Short-term Risk of Pancreatic Cancer: Results From Two Retrospective Cohort Studies.

机构信息

International Prevention Research Institute, Lyon, France.

Strathclyde Institute for Global Public Health at International Prevention Research Institute, Lyon, France.

出版信息

Diabetes Care. 2018 Feb;41(2):286-292. doi: 10.2337/dc17-0280. Epub 2017 Nov 16.

Abstract

OBJECTIVE

Concerns have been raised about a possible increased risk of pancreatic cancer associated with incretin-based therapies. We examined the risk of pancreatic cancer among patients with diabetes prescribed incretin drugs.

RESEARCH DESIGN AND METHODS

With the use of public health insurance databases of Belgium and the Lombardy Region, Italy, we created two retrospective cohorts that included adult patients who were first prescribed an incretin drug or another noninsulin antidiabetic drug (NIAD) from 1 July 2008 to 31 December 2013 in Belgium and from 1 January 2008 to 31 December 2012 in the Lombardy Region. The risk of pancreatic cancer was evaluated by multivariate-adjusted Cox models that included time-dependent variables. Adjusted hazard ratios (aHRs) from Belgium and Italy were pooled by using fixed-effects meta-analyses.

RESULTS

The cohorts included 525,733 patients with diabetes treated with NIADs and 33,292 with incretin drugs. Results in both cohorts were similar. Eighty-five and 1,589 subjects who developed pancreatic cancer were registered among the incretin and NIAD new users, respectively, which represented an aHR of pancreatic cancer of 2.14 (95% CI 1.71-2.67) among those prescribed an incretin compared with an NIAD. The aHR with a drug use lag exposure of 6 months was 1.69 (1.24-2.32). The aHR decreased from 3.35 (2.32-4.84) in the first 3 months after the first incretin prescription to 2.12 (1.22-3.66) in months 3-5.9, 1.95 (1.20-3.16) in months 6-11.9, and 1.69 (1.12-2.55) after 12 months. Among those prescribed an NIAD, pancreatic cancer occurred mostly within the year after the first prescription. The risk of pancreatic cancer among patients subsequently prescribed insulin was 6.89 (6.05-7.85).

CONCLUSIONS

The recent prescription of incretin therapy is associated with an increased risk of pancreatic cancer. The reason for such an increase is likely the consequence of an occult pancreatic cancer that provokes or aggravates diabetes. Studies are warranted for assessing the risk of pancreatic cancer associated with long-term use of incretin drugs.

摘要

目的

人们对肠促胰岛素疗法可能增加胰腺癌风险表示担忧。本研究旨在调查接受肠促胰岛素药物治疗的糖尿病患者发生胰腺癌的风险。

研究设计和方法

利用比利时和意大利伦巴第地区公共卫生保险数据库,我们创建了两个回顾性队列,包括 2008 年 7 月 1 日至 2013 年 12 月 31 日期间在比利时首次接受肠促胰岛素药物或其他非胰岛素类抗糖尿病药物(NIAD)治疗以及 2008 年 1 月 1 日至 2012 年 12 月 31 日期间在伦巴第地区首次接受肠促胰岛素药物或其他 NIAD 治疗的成年糖尿病患者。通过包含时间依赖性变量的多变量调整 Cox 模型评估胰腺癌风险。使用固定效应荟萃分析汇总来自比利时和意大利的调整后危险比(aHR)。

结果

两个队列分别纳入了 525733 例接受 NIAD 治疗的糖尿病患者和 33292 例接受肠促胰岛素药物治疗的患者。结果相似。在接受肠促胰岛素和 NIAD 新治疗的患者中,分别有 85 例和 1589 例患者确诊为胰腺癌,与接受 NIAD 治疗的患者相比,接受肠促胰岛素治疗的患者发生胰腺癌的 aHR 为 2.14(95%CI 1.71-2.67)。暴露于药物使用潜伏期 6 个月时的 aHR 为 1.69(1.24-2.32)。aHR 从首次接受肠促胰岛素治疗后的前 3 个月的 3.35(2.32-4.84)降至第 3-5.9 个月的 2.12(1.22-3.66)、第 6-11.9 个月的 1.95(1.20-3.16)和第 12 个月后的 1.69(1.12-2.55)。在接受 NIAD 治疗的患者中,胰腺癌主要发生在首次处方后 1 年内。随后处方胰岛素的患者发生胰腺癌的风险为 6.89(6.05-7.85)。

结论

近期接受肠促胰岛素治疗与胰腺癌风险增加相关。这种增加的原因可能是隐匿性胰腺癌引起或加重糖尿病的结果。有必要开展研究评估长期使用肠促胰岛素药物与胰腺癌风险的关联。

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