This post hoc analysis of a randomised phase 3 study evaluated 1879 adults with type 2 diabetes over a 40-week follow-up period. The intervention involved tirzepatide at doses of 5, 10, or 15 mg, compared with semaglutide at 1 mg. The primary outcome measured the attainment of standard and intensive therapeutic targets, defined as HbA1c less than 53 mmol/mol [7%], blood pressure less than 140/90 mmHg, LDL-cholesterol less than 1.8 mmol/l, and greater than 10% weight loss for standard targets, or HbA1c less than 48 mmol/mol [6.5%], blood pressure less than 130/80 mmHg, LDL-cholesterol less than 1.4 mmol/l, and greater than 15% weight loss for intensive targets.
All doses of tirzepatide increased the number of achieved standard and intensive targets compared with semaglutide. For standard therapeutic targets, 34% of patients on semaglutide met three or more targets, versus 42% on tirzepatide 5 mg, 53% on 10 mg, and 57% on 15 mg. For intensive therapeutic targets, 8% on semaglutide met three or more targets, versus 15% on tirzepatide 5 mg, 20% on 10 mg, and 29% on 15 mg.
Tirzepatide increased the odds of achieving specific targets, with odds ratios of 1.50 for HbA1c less than 53 mmol/mol [7%], 1.88 for HbA1c less than 48 mmol/mol [6.5%], 2.72 for weight loss greater than 10%, 3.86 for weight loss greater than 15%, and 1.45 for blood pressure less than 130/80 mmHg. Safety data, adverse events, and discontinuations were not reported. The study notes that longer trials are needed to confirm benefits on long-term prognosis.
View Original Abstract ↓
AIMS/HYPOTHESIS: Simultaneous control of HbA, lipid profile, BP and body weight is essential for preventing chronic complications of type 2 diabetes. Glucagon-like peptide-1 (GLP-1)-based therapies improve all these variables but whether the dual GLP-1 / glucose-dependent insulinotropic polypeptide (GIP) agonist tirzepatide is superior to semaglutide in attaining therapeutic targets remains unclear.
METHODS: We performed a post hoc analysis of the SURPASS-2 trial, a randomised phase 3 study including 1879 adults with type 2 diabetes. Participants were randomised to receive tirzepatide (5, 10 or 15 mg) or semaglutide (1 mg). In this analysis, we compared the effects of tirzepatide vs semaglutide on the attainment of standard (HbA <53 mmol/mol [7%], BP <140/90 mmHg, LDL-cholesterol <1.8 mmol/l, >10% weight loss) and intensive (HbA <48 mmol/mol [6.5%], BP <130/80 mmHg, LDL-cholesterol <1.4 mmol/l , >15% weight loss) therapeutic targets at 40 weeks.
RESULTS: In the SURPASS-2 trial, at baseline, 19% of participants were on target for attaining no standard goals, 59% for one goal and 21% for two or more goals. For intensive therapeutic targets, 58% of participants were on target for attaining zero goals, 38% for one goal and 4% for two goals. All doses of tirzepatide increased the number of achieved standard and intensive targets compared with semaglutide. For standard targets, 34% of participants treated with semaglutide met three or more targets, compared with 42%, 53% and 57% with tirzepatide 5, 10 and 15 mg, respectively. For intensive targets, 8% of participants treated with semaglutide met three or more targets, vs 15%, 20% and 29% with tirzepatide. Regarding specific therapeutic goals, tirzepatide increased the odds of achieving standard and intensive targets for HbA (HbA <53 mmol/mol [7%], OR 1.50 [95% CI 1.12, 2.00]; HbA <48 mmol/mol [6.5%], OR 1.88 [95%CI 1.49, 2.36]) and weight loss (weight loss >10%, OR 2.72 [95% CI 2.14, 3.47]; weight loss >15%, OR 3.86 [95% CI 2.69, 5.55]) and the intensive target for BP (OR 1.45 [95% CI 1.17, 1.81]).
CONCLUSIONS/INTERPRETATION: Tirzepatide improves therapeutic target attainment compared with semaglutide in type 2 diabetes. Longer trials are needed to confirm benefits on long-term prognosis.
DATA AVAILABILITY: Data for this post hoc analysis was accessed through the Vivli (Center for Global Clinical Research Data) platform ( https://vivli.org ) with the Vivli ID 00009964.