McEwan Phil, Bøg Martin, Faurby Mads, Foos Volker, Lingvay Ildiko, Lübker Christopher, Miller Ryan, Toliver Joshua C, Yeates Florian, Lincoff A Michael
Health Economics, Health Economics and Outcomes Research Ltd, Cardiff, UK.
Novo Nordisk A/S, Bagsværd, Denmark.
J Med Econ. 2025 Dec;28(1):268-278. doi: 10.1080/13696998.2025.2459529. Epub 2025 Feb 12.
The cardioprotective effects of semaglutide 2.4 mg reported in the SELECT cardiovascular (CV) outcomes trial (ClinicalTrials.gov NCT03574597) provide clinical benefit for subjects with overweight or obesity and established CV disease without type 2 diabetes (T2D). We assessed cost-effectiveness of semaglutide 2.4 mg in this population against the American College of Cardiology/American Heart Association value framework.
A cohort-level Markov-state cost-effectiveness model using trial-derived data with outcomes from a healthcare sector perspective measured over a lifetime horizon was developed. Treatment costs were based on US list prices; scenario analyses used literature-reported estimated rebates. Healthcare costs and benefits were discounted at 3.0%. A simulated cohort of 100,000 subjects was aligned to the SELECT trial population baseline characteristics and time-on-treatment. Subjects received either semaglutide 2.4 mg or placebo in addition to standard of care (SoC). Modelled outcomes included clinical events (CV events, progression to T2D, chronic kidney disease [CKD]) and health economic measures, including direct costs and quality-adjusted life years (QALYs).
Mean semaglutide 2.4 mg treatment duration was 2.79 years. Per 100,000 subjects, treatment avoided 2,791 non-fatal myocardial infarctions, 3,000 coronary revascularizations, 487 non-fatal strokes, and 115 CV deaths over the modeled lifetime horizon. Average per-subject lifetime treatment costs were $47,353; savings arose from avoided T2D ($14,431), CKD ($2,074), and CV events ($1,512). Semaglutide 2.4 mg was associated with increased lifetime costs ($29,767), additional QALYs gained (0.218) and an incremental cost-effectiveness ratio of $136,271/QALY at list price; a scenario using an empirically estimated 48% rebate predicted $32,219/QALY.
The generalizability of observations from SELECT to a broader US population is unknown. Our model does not capture all outcomes nor costs that may be affected by weight loss. Modeling assumptions may present limitations.
Semaglutide 2.4 mg use as in SELECT is cost-effective at list price, using a $150,000/QALY willingness-to-pay threshold.
SELECT心血管(CV)结局试验(ClinicalTrials.gov NCT03574597)报告的司美格鲁肽2.4mg的心脏保护作用为超重或肥胖且患有确诊CV疾病但无2型糖尿病(T2D)的受试者提供了临床益处。我们根据美国心脏病学会/美国心脏协会的价值框架评估了司美格鲁肽2.4mg在该人群中的成本效益。
开发了一个队列水平的马尔可夫状态成本效益模型,该模型使用试验衍生数据,从医疗保健部门的角度衡量终身范围内的结局。治疗成本基于美国标价;情景分析使用文献报道的估计回扣。医疗保健成本和效益按3.0%进行贴现。一个由100,000名受试者组成的模拟队列与SELECT试验人群的基线特征和治疗时间相匹配。受试者除接受标准治疗(SoC)外,还接受司美格鲁肽2.4mg或安慰剂治疗。模拟的结局包括临床事件(CV事件、进展为T2D、慢性肾脏病[CKD])和健康经济指标,包括直接成本和质量调整生命年(QALY)。
司美格鲁肽2.4mg的平均治疗持续时间为2.79年。在模拟的终身范围内,每100,000名受试者中,治疗避免了2,791例非致命性心肌梗死、3,000例冠状动脉血运重建、487例非致命性中风和115例CV死亡。每位受试者的平均终身治疗成本为47,353美元;因避免T2D(14,431美元)、CKD(2,07