1º Encontro de Departamentos da Cardiologia

Dados do Trabalho


Título

Modelling Long-term Outcomes of Tirzepatide Compared to Lifestyle Management and other Anti-Obesity Medications as Treatment for Overweight and Obesity

Resumo

  Introduction SURMOUNT-1 demonstrated significant weight reduction and improvement in cardiometabolic risk factors with tirzepatide treatment, but data beyond 72 weeks are currently unavailable for people with overweight and obesity without T2DM. Objectives This study uses a patient-level simulation (PLS) to estimate long-term clinical outcomes with tirzepatide versus relevant comparators.  Methods A PLS was implemented in the discretely-integrated condition-event (DICE) framework, which considers patient heterogeneity and event history. NHANES data, filtered to match FDA guidance for obesity treatment excluding patients with T2DM, supplied baseline patient characteristics. The model used published data to simulate the impact of tirzepatide and key comparators on BMI. Simulated metabolic factor (i.e., BMI, HDL, SBP, and fasting plasma glucose) trajectories were inputs to published risk equations that estimate risk of key obesity-related complications: cardiovascular events (Framingham 10-year risk estimate) and onset of type 2 diabetes (T2DM; Framingham Offspring study). Health-related quality of life was linked to BMI and complications over time. All comparators were modeled at the highest indicated dose. Results Versus semaglutide, phentermine/topiramate, naltrexone/buproprion, and lifestyle modification (LSM), the model predicted tirzepatide increases life expectancy by 0.16, 0.30, 0.36, and 0.69 years, and increases quality-adjusted life expectancy by 0.61, 0.92, 1.46, and 2.10 QALYs, respectively. Tirzepatide is predicted to decrease event rates and increase average time to onset of modeled obesity-related complications. Specifically, the model predicted tirzepatide reduced the percentage of patients with any cardiovascular event compared to semaglutide, phentermine/topiramate, naltrexone/buproprion and LSM by 3.6%, 4.6%, 6.8% and 10.7% respectively, and delayed time to onset of T2DM by 0.17, 0.78, 2.39, and 3.70 years, respectively. A similar pattern of benefit is seen for lower tirzepatide doses. Conclusion Long-term projections using SURMOUNT-1 data in a validated model showed people with overweight and obesity treated with tirzepatide are likely to have longer life expectancy, experience improved quality-of-life, and decreased incidence of obesity-related complications.   © 2023 International Society for Pharmacoeconomics and Outcomes Research. Reused with permission. This abstract was accepted and previously presented at the ISPOR Europe 2023 conference; Copenhagen, Denmark. All rights reserved.

Palavras Chave

Tirzepatide; Cardiometabolic risk; weight control

Área

APRESENTAÇÕES PATROCINADAS / INDÚSTRIA FARMACÊUTICA

Categoria

Pesquisador

Autores

MEREDITH M HOOG, HONG KAN, KRISTEN DEGER, SONJA SORENSEN, LISA M NEFF, JAY PATRICK BAE, EMILY RUTH HANKOSKY, DONNA MOJDAMI, BENJAMIN WHITE, MACK HARRIS, PEDRO VELLOSA SCHWARTZMANN