IDH2型
耐火材料(行星科学)
医学
成本效益
内科学
置信区间
肿瘤科
突变体
IDH1
生物
风险分析(工程)
天体生物学
基因
生物化学
作者
Abdulrahman Alhajahjeh,Kishan Patel,Rory M. Shallis,Nikolai A. Podoltsev,Tariq Kewan,Jessica M. Stempel,Lourdes M. Mendez,Scott F. Huntington,Maximilian Stahl,George Goshua,Jan Philipp Bewersdorf,Amer M. Zeidan
标识
DOI:10.1080/10428194.2024.2426073
摘要
In the randomized phase III IDHENTIFY trial, the IDH2 inhibitor enasidenib (ENA) showed improvement in event-free but not overall survival compared with conventional care regimens (CCR) among patients with relapsed/refractory (R/R), IDH2-mutant AML. We constructed a partitioned survival model to evaluate the cost-effectiveness of enasidenib for the treatment of older patients with R/R, and IDH2-mutant AML. In the base-case scenario, ENA exhibited an incremental effectiveness of 0.234quality-adjusted life-years (QALYs) compared to CCR, and an incremental cost of $126,800, leading to an incremental cost-effectiveness ratio of $540,300/QALY(95% CI: $197,800–$4,777,000/QALY). In probabilistic sensitivity analysis, CCR was favored in 99.8% of simulations. The cost of ENA would need to be decreased by 72% to be cost-effective at a willingness-to-pay threshold of $150,000/QALY. Our findings suggest that ENA is unlikely to be a cost-effective treatment for older patients with IDH2-mutant R/R AML under current pricing.
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