一项更新的成本-效用模型:onasemnogene abeparvovec (Zolgensma®)治疗1型脊髓性肌萎缩症患者,并与临床与有效性审查研究所(ICER)的评估进行比较。

Rebecca Dean, Ivar Jensen, Phil Cyr, Beckley Miller, Benit Maru, Douglas M Sproule, Douglas E Feltner, Thomas Wiesner, Daniel C Malone, Matthias Bischof, Walter Toro, Omar Dabbous
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Updated quality-adjusted survival using ICER's utility scores and discounted at 3% were 13.33, 2.85, and 1.15 discounted QALYs for onasemnogene abeparvovec, nusinersen, and BSC, respectively. Using estimated net prices, the discounted lifetime cost/patient was $3.93 M for onasemnogene abeparvovec, $4.60 M for nusinersen, and $1.96 M for BSC. The incremental cost per QALY gained for onasemnogene abeparvovec was dominant against nusinersen and $161,648 against BSC. These results broadly align with the results of the ICER model, which predicted a cost per QALY gained of $139,000 compared with nusinersen, and $243,000 compared with BSC (assuming a placeholder price of $2 M for onasemnogene abeparvovec), differences in methodology notwithstanding. Exploratory analyses in presymptomatic patients were similar. <b>Conclusion</b>: This updated CUA model is similar to ICER analyses comparing onasemnogene abeparvovec with nusinersen in the symptomatic and presymptomatic SMA populations. 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引用次数: 23

摘要

背景:最近用于治疗1型脊髓性肌萎缩症(SMA1)的onasemnogene abeparvovec (Zolgensma®,前身为AVXS-101)的成本效用分析(CUA)模型在关键假设和结果上存在差异。目的:比较制造商的专有CUA模型与临床与经济评论研究所(ICER)发表的模型,并利用长期随访数据和一些关键的ICER假设来更新制造商的模型。研究设计:我们更新了最近的一项CUA,评估在症状性SMA1患者中,onasemnogene abparvovec与nusinersen (Spinraza®)或最佳支持治疗(BSC)的每增量质量调整生命年(QALY)的成本价值,并将其与ICER模型进行比较。干预措施:单剂量基因替代疗法Onasemnogene abeparvovec与反义寡核苷酸nusinersen与BSC。主要结果测量:增量成本效益比和基于价值的价格,使用美国普通药物的传统阈值。结果:该模型预测onasemnogene abeparvovec的更新生存期(未打折)为37.60年,而nusinersen和BSC的更新生存期分别为12.10年和7.27年。使用ICER效用评分和3%折现的更新质量调整生存率对于onasemnogene abeparvovec、nusinersen和BSC分别为13.33、2.85和1.15折现QALYs。使用估计净价格,onasemnogene abeparvovec的折扣终身成本为393万美元,nusinersen为460万美元,BSC为196万美元。与nusinsen相比,单基因abparvovec获得的每QALY增量成本占主导地位,而与BSC相比,增量成本为161,648美元。这些结果与ICER模型的结果大致一致,ICER模型预测与nusinersen相比,每个QALY获得的成本为139,000美元,与BSC相比为243,000美元(假设onasemnogene abparvovec的占位符价格为200万美元),尽管方法存在差异。对症状前患者的探索性分析结果相似。结论:这个更新的CUA模型类似于ICER分析,比较了症状性和症状前SMA人群中onasemnogene abeparvovec和nusinsen。对于2岁前治疗的SMA1患者,onasemnogene abparvovec的标价为212.5万美元,与nusinersen相比具有成本效益。与BSC相比,onasemnogene abeparvovec的每个QALY成本高于美国常用的治疗阈值(每个QALY 150,000美元)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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An updated cost-utility model for onasemnogene abeparvovec (Zolgensma®) in spinal muscular atrophy type 1 patients and comparison with evaluation by the Institute for Clinical and Effectiveness Review (ICER).

Background: Recent cost-utility analysis (CUA) models for onasemnogene abeparvovec (Zolgensma®, formerly AVXS-101) in spinal muscular atrophy type 1 (SMA1) differ on key assumptions and results. Objective: To compare the manufacturer's proprietary CUA model to the model published by the Institute for Clinical and Economic Review (ICER), and to update the manufacturer's model with long-term follow-up data and some key ICER assumptions. Study design: We updated a recent CUA evaluating value for money in cost per incremental Quality-adjusted Life Year (QALY) of onasemnogene abeparvovec versus nusinersen (Spinraza®) or best supportive care (BSC) in symptomatic SMA1 patients, and compared it to the ICER model. Setting/Perspective: USA/Commercial payer Participants: Children aged <2 years with SMA1. Interventions: Onasemnogene abeparvovec, a single-dose gene replacement therapy, versus nusinersen, an antisense oligonucleotide, versus BSC. Main outcome measure: Incremental-cost effectiveness ratio and value-based price using traditional thresholds for general medicines in the US. Results: Updated survival (undiscounted) predicted by the model was 37.60 years for onasemnogene abeparvovec compared to 12.10 years for nusinersen and 7.27 years for BSC. Updated quality-adjusted survival using ICER's utility scores and discounted at 3% were 13.33, 2.85, and 1.15 discounted QALYs for onasemnogene abeparvovec, nusinersen, and BSC, respectively. Using estimated net prices, the discounted lifetime cost/patient was $3.93 M for onasemnogene abeparvovec, $4.60 M for nusinersen, and $1.96 M for BSC. The incremental cost per QALY gained for onasemnogene abeparvovec was dominant against nusinersen and $161,648 against BSC. These results broadly align with the results of the ICER model, which predicted a cost per QALY gained of $139,000 compared with nusinersen, and $243,000 compared with BSC (assuming a placeholder price of $2 M for onasemnogene abeparvovec), differences in methodology notwithstanding. Exploratory analyses in presymptomatic patients were similar. Conclusion: This updated CUA model is similar to ICER analyses comparing onasemnogene abeparvovec with nusinersen in the symptomatic and presymptomatic SMA populations. At a list price of $2.125 M, onasemnogene abeparvovec is cost-effective compared to nusinersen for SMA1 patients treated before age 2 years. When compared to BSC, cost per QALY of onasemnogene abeparvovec is higher than commonly used thresholds for therapies in the USA ($150,000 per QALY).

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