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利用钠-葡萄糖协同转运蛋白2抑制剂研究癌症风险:世界卫生组织全球药物警戒数据库Vigibase中的不成比例性分析

Investigating Risk of Cancer with Sodium-Glucose Cotransporter 2 Inhibitors: A Disproportionality Analysis in the WHO Global Pharmacovigilance Database Vigibase.

作者信息

Gautier Paul, Elbaz Meyer, Bouisset Frédéric, Despas Fabien, Montastruc François

机构信息

Department of Medical and Clinical Pharmacology, Faculty of Medicine, Centre of PharmacoVigilance and Pharmacoepidemiology, Toulouse University Hospital (CHU), 37 Allées Jules Guesde, 31000, Toulouse, France.

Team PEPSS (Pharmacologie En Population cohorteS et biobanqueS), Centre d'Investigation Clinique 1436, Toulouse University Hospital, Toulouse, France.

出版信息

Drug Saf. 2025 Apr 15. doi: 10.1007/s40264-025-01546-5.

Abstract

INTRODUCTION

Use of sodium-glucose cotransporter 2 inhibitors (SGLT-2is) has significantly increased due to their cardiovascular benefits. Whether SGLT-2is increase risk of cancer has been of concern since first clinical trials, but this question remains unclear because of methodological limitations in previous studies.

METHODS

We conducted a disproportionality analysis using Vigibase between 2014 and 2023 to estimate the association between SGLT-2i use and the risk of reporting of different subtypes of cancers, compared with glucagon like peptide-1 (GLP-1) analogues and dipeptidyl peptidase-4 (DPP-4) inhibitors.

RESULTS

Among 644 reported cases of cancer associated with SGLT-2i use, 427 (66.3%) were male, with a mean age of 66.5 ± 9.7 years. Sodium-glucose cotransporter 2 inhibitors showed increased reporting odds ratio for bladder cancer (ROR 4.46, 95% CI 3.23-6.17) and kidney cancer (ROR 1.84, 95% CI 1.25-2.69), but not for all other cancer subtypes.

CONCLUSION

In this disproportionality analysis with a hypothesis-generating approach, SGLT-2is are associated with an increased risk of reporting bladder and kidney cancer. There is a need of an urgent clarification of this signal with further long-term observational studies.

摘要

引言

由于钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2i)具有心血管益处,其使用量显著增加。自首次临床试验以来,SGLT-2i是否会增加癌症风险一直备受关注,但由于先前研究存在方法学局限性,这个问题仍不明确。

方法

我们在2014年至2023年期间使用Vigibase进行了不成比例分析,以估计SGLT-2i的使用与不同癌症亚型报告风险之间的关联,并与胰高血糖素样肽-1(GLP-1)类似物和二肽基肽酶-4(DPP-4)抑制剂进行比较。

结果

在644例报告的与SGLT-2i使用相关的癌症病例中,427例(66.3%)为男性,平均年龄为66.5±9.7岁。钠-葡萄糖协同转运蛋白2抑制剂显示膀胱癌(报告比值比4.46,95%置信区间3.23-6.17)和肾癌(报告比值比1.84,95%置信区间1.25-2.69)的报告比值增加,但其他癌症亚型并非如此。

结论

在这项采用假设生成方法的不成比例分析中,SGLT-2i与膀胱癌和肾癌报告风险增加相关。需要通过进一步的长期观察性研究紧急澄清这一信号。

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