GLP-1 Receptor Agonists Tied to Better Outcomes in Certain Patients With Breast Cancer
via HealthDayTUESDAY, May 19, 2026 -- Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are associated with better outcomes among patients with breast cancer and obesity or type 2 diabetes, according to a study published online May 11 in JAMA Network Open.
Kristina L. Tatum, Psy.D., from Virginia Commonwealth University (VCU) in Richmond, and colleagues examined whether the use of GLP-1 RAs impacts female breast cancer survival or cancer recurrence among patients with obesity or type 2 diabetes. The analysis included 1,610 matched patients with obesity and GLP-1 RA use versus nonuse, 2,323 patients with type 2 diabetes and GLP-1 RA use versus insulin or metformin, and 4,052 patients with type 2 diabetes and GLP-1 RA use versus sodium-glucose cotransporter 2 inhibitor use.
The researchers found that among patients with obesity, GLP-1 RAs were associated with a lower hazard of all-cause mortality (hazard ratio [HR], 0.35) and recurrence-free survival (RFS; HR, 0.44) over a 10-year follow-up period. Among patients with type 2 diabetes, GLP-1 RAs were associated with a lower hazard of all-cause mortality (HR, 0.09) and RFS (HR, 0.33) versus insulin or metformin. There were no significant differences between GLP-1 RA and sodium-glucose cotransporter 2 inhibitor groups. Similar findings were seen in subgroup and landmark analyses.
"This study suggests that GLP-1 drugs may offer protective benefits, potentially improving survival and recurrence risk in some female patients with breast cancer -- whether this is related to weight control, improved cardiovascular health, or other mechanisms remains to be studied," senior author Bernard F. Fuemmeler, Ph.D., also from VCU, said in a statement.
Disclaimer: Statistical data in medical articles provide general trends and do not pertain to individuals. Individual factors can vary greatly. Always seek personalized medical advice for individual healthcare decisions.
Source: HealthDay
Posted : 2026-05-20 02:48
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