Javanbakht Mehdi, Fishman Jesse, Moloney Eoin, Rydqvist Peter, Ansaripour Amir
Optimax Access Ltd, Kenneth Dibben House, Enterprise Rd, Chilworth, Southampton Science Park, Southampton, SO16 7NS, UK.
Madrigal Pharmaceuticals, Inc., West Conshohocken, PA, USA.
Pharmacoecon Open. 2023 Jan;7(1):93-110. doi: 10.1007/s41669-022-00370-2. Epub 2022 Sep 14.
Nonalcoholic steatohepatitis (NASH) is characterized by inflammation and hepatocellular damage caused by accumulation of fat in the liver. Resmetirom (MGL-3196) is an orally administered, small-molecule, liver-targeted, selective thyroid hormone receptor-β agonist. This early analysis explored the potential cost effectiveness of resmetirom for the treatment of NASH from a US commercial payer perspective.
An early economic model was developed to reflect the clinical pathways typically followed by patients with NASH and liver fibrosis. Use of resmetirom, compared with placebo, was assessed. The Markov model structure was informed by a previous modeling study and a randomized, double-blind, placebo-controlled, phase II trial of resmetirom. Costs and outcomes were assessed over a lifetime time horizon with results presented in terms of cost per quality-adjusted life-year (QALY) gained.
Resmetirom treatment resulted in increased costs of US$66,764 per patient, while increasing QALYs by 1.24. The incremental cost-effectiveness ratio was US$53,929 per QALY gained, indicating resmetirom treatment would potentially be cost effective at a willingness-to-pay (WTP) threshold of US$100,000. Results indicated that resmetirom would reduce the lifetime number of cases of decompensated cirrhosis (- 87), hepatocellular carcinoma (- 59), and liver transplants (- 30) per 1,000 patients compared with placebo. Resmetirom treatment remained cost effective at a US$100,000 WTP threshold up to a daily price point of US$72.00.
Resmetirom is a potentially cost-effective treatment option for patients with NASH and liver fibrosis based on an analysis performed from a US commercial payer perspective. Future economic analyses of the technology should, however, focus on overcoming the limitations of existing modeling methodology.
非酒精性脂肪性肝炎(NASH)的特征是肝脏中脂肪堆积导致炎症和肝细胞损伤。瑞美替隆(MGL-3196)是一种口服的小分子肝脏靶向选择性甲状腺激素受体β激动剂。本早期分析从美国商业支付方的角度探讨了瑞美替隆治疗NASH的潜在成本效益。
建立了一个早期经济模型,以反映NASH和肝纤维化患者通常遵循的临床路径。评估了瑞美替隆与安慰剂相比的使用情况。马尔可夫模型结构基于之前的建模研究以及瑞美替隆的一项随机、双盲、安慰剂对照的II期试验。在终身时间范围内评估成本和结果,结果以每获得一个质量调整生命年(QALY)的成本表示。
瑞美替隆治疗使每位患者的成本增加66,764美元,同时使QALY增加1.24。增量成本效益比为每获得一个QALY 53,929美元,这表明在支付意愿(WTP)阈值为100,000美元时,瑞美替隆治疗可能具有成本效益。结果表明,与安慰剂相比,瑞美替隆将使每1000名患者的失代偿性肝硬化、肝细胞癌和肝移植的终身病例数分别减少87例、59例和30例。在WTP阈值为100,000美元且每日价格达到72.00美元之前,瑞美替隆治疗仍具有成本效益。
基于从美国商业支付方角度进行的分析,瑞美替隆对于NASH和肝纤维化患者是一种潜在的具有成本效益的治疗选择。然而,该技术未来的经济分析应侧重于克服现有建模方法的局限性。