Sarker Jyotirmoy, Tice Jeffrey A, Rind David M, Pearson Steven D, Walton Surrey M
Department of Pharmacy Systems, Outcomes, and Policy, University of Illinois Chicago College of Pharmacy.
Division of General Internal Medicine, University of California San Francisco.
J Manag Care Spec Pharm. 2024 Aug;30(8):868-872. doi: 10.18553/jmcp.2024.30.8.868.
This viewpoint discusses cost-effectiveness estimates for EtranaDez, a gene therapy for hemophilia B, using the Institute for Clinical and Economic Review's (ICER) framework for single and short-term therapies (SSTs). EtranaDez offers long-term benefits from a single administration, in contrast to the high costs and frequent dosing required by current factor IX prophylaxis. However, the projected gains in health from EtranaDez are small relative to the cost implications of the therapy, and consequently, how the cost offsets associated with EtranaDez are counted has a substantial impact on assessing its cost-effectiveness. Strategies for assessing cost offsets used in the ICER SST framework include a 50/50 cost-sharing model between the health care system and the manufacturer and a cap of $150,000 annually on health care cost offsets. Results from the standard full cost-offset analysis as reported by ICER depicted EtranaDez as a dominant therapy with substantial cost savings compared with factor IX prophylaxis. However, while considering the ICER SST framework, particularly the $150,000 annual cap scenario, the cost-effectiveness was significantly reduced. The incremental cost-effectiveness ratio varied notably between these scenarios, challenging the conventional perception of value of gene therapy in health care. These cost-sharing scenarios highlight the potential of the ICER SST framework to help curtail inefficient health care spending. In cases in which the cost of existing treatment is exceedingly high, the application of such frameworks would improve efficiency in resource allocation, fostering a balance between incentives for innovation and economic sustainability in managed care systems.
本观点使用临床与经济评论研究所(ICER)的单疗程和短期疗法(SSTs)框架,讨论了用于治疗B型血友病的基因疗法EtranaDez的成本效益评估。与目前的凝血因子IX预防性治疗所需的高成本和频繁给药相比,EtranaDez单次给药即可带来长期益处。然而,相对于该疗法的成本影响而言,EtranaDez预计带来的健康收益较小,因此,如何计算与EtranaDez相关的成本抵消对评估其成本效益有重大影响。ICER SST框架中用于评估成本抵消的策略包括医疗保健系统与制造商之间50/50的成本分摊模式,以及每年15万美元的医疗保健成本抵消上限。ICER报告的标准全额成本抵消分析结果显示,与凝血因子IX预防性治疗相比,EtranaDez是一种具有显著成本节约的优势疗法。然而,在考虑ICER SST框架,特别是每年15万美元上限的情况下,成本效益显著降低。这些情景下的增量成本效益比差异显著,挑战了基因疗法在医疗保健领域价值的传统认知。这些成本分摊情景凸显了ICER SST框架在帮助减少低效医疗支出方面的潜力。在现有治疗成本极高的情况下,应用此类框架将提高资源分配效率,在管理式医疗系统中促进创新激励与经济可持续性之间的平衡。