Zomer Ella, Zhou Jennifer, Nelson Adam J, Sumithran Priya, Nanayakkara Shane, Ball Jocasta, Kaye David, Liew Danny, Nicholls Stephen J, Stub Dion, Zoungas Sophia
School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, Victoria 3004, Australia.
Department of Cardiology, Alfred Hospital, Melbourne, Victoria, Australia.
Eur Heart J Qual Care Clin Outcomes. 2025 Sep 12;11(6):857-867. doi: 10.1093/ehjqcco/qcae063.
The Semaglutide Effects on Cardiovascular Outcomes in People with Overweight or Obesity (SELECT) trial demonstrated significant reductions in cardiovascular outcomes in people with cardiovascular disease (CVD) and overweight or obesity (but without diabetes). However, the cost of the medication has raised concerns about its financial viability and accessibility within healthcare systems. This study explored whether the use of semaglutide for the secondary prevention of CVD in overweight or obesity is cost-effective from the Australian healthcare perspective.
A Markov model was developed based on the SELECT trial to model the clinical outcomes and costs of a hypothetical population treated with semaglutide vs. placebo, in addition to standard care, and followed up over 20 years. With each annual cycle, subjects were at risk of having non-fatal CVD events or dying. Model inputs were derived from SELECT and published literature. Costs were obtained from Australian sources. All outcomes were discounted by 5% annually. The main outcome of interest was the incremental cost-effectiveness ratio (ICER) in terms of cost per year of life saved (YoLS) and cost per quality-adjusted life year (QALY) gained. With an annual estimated cost of semaglutide of A$4175, the model resulted in ICERs of A$99 853 (US$143 504; £40 873) per YoLS and A$96 055 (US$138 046; £39 318) per QALY gained.
Assuming a willingness-to-pay threshold of A$50 000, semaglutide is not considered cost-effective at the current price. A price of ≤A$2000 per year or more targeted use in high-risk patients would be needed for it to be considered cost-effective in the Australian setting.
司美格鲁肽对超重或肥胖人群心血管结局的影响(SELECT)试验表明,患有心血管疾病(CVD)且超重或肥胖(但无糖尿病)的人群心血管结局显著降低。然而,该药物的成本引发了人们对其在医疗保健系统中的财务可行性和可及性的担忧。本研究从澳大利亚医疗保健的角度探讨了使用司美格鲁肽对超重或肥胖人群进行CVD二级预防是否具有成本效益。
基于SELECT试验开发了一个马尔可夫模型,以模拟接受司美格鲁肽与安慰剂治疗的假设人群的临床结局和成本,此外还包括标准治疗,并随访20年。在每个年度周期中,受试者都有发生非致命性CVD事件或死亡的风险。模型输入数据来自SELECT试验和已发表的文献。成本数据来自澳大利亚。所有结局每年按5%进行贴现。主要关注的结局是以每挽救一年生命(YoLS)的成本和每获得一个质量调整生命年(QALY)的成本来计算增量成本效益比(ICER)。司美格鲁肽的年估计成本为4175澳元,该模型得出的ICER为每YoLS 99853澳元(143504美元;40873英镑),每获得一个QALY为96055澳元(138046美元;39318英镑)。
假设支付意愿阈值为50000澳元,按当前价格,司美格鲁肽不被认为具有成本效益。在澳大利亚的情况下,若要使其被认为具有成本效益,每年价格需≤2000澳元,或在高危患者中更有针对性地使用。