Risk for Cancer With Glucagon-Like Peptide-1 Receptor Agonists and Dual Agonists : A Systematic Review and Meta-analysis
Department
Internal Medicine
Document Type
Article
Publication Title
Annals of Internal Medicine
Abstract
Background: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are used for type 2 diabetes mellitus (T2DM) and overweight or obesity, but their association with cancer is unclear.
Purpose: To investigate the risk for obesity-related cancer associated with GLP-1RAs.
Data sources: PubMed, Embase, Web of Science, Scopus, and the Cochrane Central Register of Controlled Trials from inception to August 2025.
Study selection: Randomized placebo-controlled trials reporting any of the following cancer outcomes: thyroid, pancreatic, colorectal, gastric, esophageal, liver, gallbladder, breast, ovarian, endometrial, or kidney cancer; multiple myeloma; or meningioma.
Data extraction: Risk of bias was evaluated using the Cochrane Risk of Bias 2 tool, and certainty of evidence was assessed using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) approach. Odds ratios (ORs) were pooled using random-effects meta-analysis.
Data synthesis: The review included 48 trials involving 94 245 participants. GLP-1RAs probably have little or no effect on risk for thyroid cancer (OR, 1.37 [95% CI, 0.82 to 2.31]; 1 fewer to 9 more cases per 10 000 patients treated), pancreatic cancer (OR, 0.84 [CI, 0.53 to 1.35]; 9 fewer to 6 more per 10 000), breast cancer (OR, 0.95 [CI, 0.60 to 1.49]; 10 fewer to 12 more per 10 000), or kidney cancer (OR, 1.12 [CI, 0.78 to 1.60]; 5 fewer to 13 more per 10 000) (moderate certainty). GLP-1RAs may have little or no effect on colorectal, esophageal, liver, gallbladder, ovarian, or endometrial cancer; multiple myeloma; or meningioma (low certainty). The effect on gastric cancer is very uncertain. Results were consistent in sensitivity analyses of trials with low risk of bias and studies of semaglutide or tirzepatide and across subgroups stratified by follow-up duration, population, GLP-1RA class, weight loss profile, dose, and duration of action.
Limitation: The included trials were not designed to evaluate cancer outcomes and had short follow-up.
Conclusion: GLP-1RAs may have little or no effect on risk for obesity-related cancers. Longer-term studies are needed to clarify potential risks or benefits.
First Page
216
Last Page
229
DOI
10.7326/ANNALS-25-02237
Volume
179
Issue
2
Publication Date
2-1-2026
Publisher
American College of Physicians--American Society of Internal Medicine
Medical Subject Headings
Humans; Glucagon-Like Peptide-1 Receptor Agonists; Neoplasms; Hypoglycemic Agents; Diabetes Mellitus, Type 2; Obesity; Randomized Controlled Trials as Topic
PubMed ID
41359966
Recommended Citation
Ko, A., Chang, Y., Bahar, F., Wang, T., Xanthavanij, N., Yu, C., Hsieh, R., See, X., Lo, S., Song, J., Hsia, Y., Chiang, C., Xu, X., Lin, S., & Chiang, C. (2026). Risk for Cancer With Glucagon-Like Peptide-1 Receptor Agonists and Dual Agonists : A Systematic Review and Meta-analysis. Annals of Internal Medicine, 179 (2), 216-229. https://doi.org/10.7326/ANNALS-25-02237