Do GLP-1 Receptor Agonists Increase the Risk of Breast Cancer? A Systematic Review and Meta-analysis

• Published in: The journal of clinical endocrinology and metabolism 2021-03, Vol.106 (3), p.912-921
• Main Authors: Piccoli, Giovana F, Mesquita, Leonardo A, Stein, Cinara, Aziz, Marina, Zoldan, Maira, Degobi, Nathália A H, Spiazzi, Bernardo F, Lopes Junior, Gilberto L, Colpani, Verônica, Gerchman, Fernando
• Format: Article
• Language: English
• Subjects: Agonists; Breast cancer; Care and treatment; Clinical trials; Development and progression; Diabetes; Diabetes mellitus; Diabetes therapy; Drug development; GLP-1 receptor agonists; Glucagon; Glucagon-like peptide 1; Health aspects; Liraglutide; Medical research; Medicine, Experimental; Meta-analysis; Obesity; Risk factors; Tumors; Type 2 diabetes
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/clinem/dgaa891

Abstract Context Risk of cancer is a major concern in the development of drugs for the treatment of obesity and diabetes. In randomized controlled trials (RCTs) of the Liraglutide Clinical Development Program, subjects treated with a glucagon-like peptide-1 receptor agonist (GLP-1RA) had a higher absolute number of breast cancer events. Objective To assess whether patients treated with GLP-1RAs had a higher risk of breast neoplasms. Data Sources We searched MEDLINE, Embase, Web of Science, and CENTRAL from July 31, 2019 to February 8, 2020. Study Selection Reviewers assessed abstracts and full-text articles for RCTs of GLP-1RAs in adults with excessive weight and/or diabetes and a minimum follow-up of 24 weeks. Data Extraction Researchers extracted study-level data and assessed within-study risk of bias with the RoB 2.0 tool and quality of evidence with Grading of Recommendations Assessment, Development and Evaluation (GRADE). Data Synthesis We included 52 trials, of which 50 reported breast cancer events and 11 reported benign breast neoplasms. Overall methodological quality was high. Among 48 267 subjects treated with GLP-1RAs, 130 developed breast cancer compared with 107 of 40 755 controls (relative risk [RR], 0.98; 95% confidence interval [CI], 0.76–1.26). Subset analyses according to follow-up, participant/investigator blinding, and type of GLP-1RA did not reveal any differences. The risk of benign breast neoplasms also did not differ between groups (RR, 0.99; 95% CI, 0.48–2.01). Trial sequential analysis provided evidence that the sample size was sufficient to avoid missing alternative results. Conclusions Treatment with GLP-1RAs for obesity and diabetes does not increase the risk of breast neoplasms.