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A meta-analysis of serious adverse events reported with exenatide and liraglutide: acute pancreatitis and cancer.

Diabetes Res Clin Pract · 2012

Last updated 2026-05-28

A review of 25 studies found no clear link between the GLP-1 drugs exenatide or liraglutide and an increased risk of acute pancreatitis or any type of cancer. For thyroid cancer specifically, liraglutide showed no increased risk, and no thyroid cancer cases were reported with exenatide. The results suggest current evidence is not strong enough to confirm these risks.

AI summary of the abstract below.

JournalDiabetes Res Clin Pract, 2012
Citations146
Relative citation ratio4.69
NIH percentile92
Molecules liraglutide, exenatide

Abstract

AIMS: The association between GLP-1 agonists, acute pancreatitis (AP), any cancer and thyroid cancer is discussed. This meta-analysis was aimed at evaluating the risk of those serious adverse events associated with GLP-1 agonists in patients with type 2 diabetes. METHODS: Medline, EMBASE, Cochrane Library and clinicaltrials.gov were searched in order to identify longitudinal studies evaluating exenatide or liraglutide use and reporting data on AP or cancer. Odds ratios (ORs) were pooled using a random-effects model. I(2) statistics assessed heterogeneity. RESULTS: Twenty-five studies were included. Neither exenatide (OR 0.84 [95% CI 0.58-1.22], I(2) = 30%) nor liraglutide (OR 0.97 [95% CI 0.21-4.39], I(2) = 0%) were associated with an increased risk of AP, independent of baseline comparator. The pooled OR for cancer associated with exenatide was 0.86 (95% CI 0.29, 2.60, I(2) = 0%) and for liraglutide was 1.35 (95% CI 0.70, 2.59, I(2) = 0%). Liraglutide was not associated with an increased risk for thyroid cancer (OR 1.54 [95% CI 0.40-6.02], I(2) = 0%). For exenatide, no thyroid malignancies were reported. CONCLUSIONS: Current available published evidence is insufficient to support an increased risk of AP or cancer associated with GLP-1 agonists. These rare and long-term adverse events deserve properly monitoring in future studies evaluating GLP-1 agonists.

Verbatim abstract via PubMed 23010561 ↗

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