Cost-effectiveness analysis of dupilumab among patients with uncontrolled severe asthma using LIBERTY ASTHMA QUEST Korean data.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-08-26 DOI:10.1186/s13561-024-00532-4
Sung-Hee Oh, Chin Kook Rhee, Eun Jin Bae, Hyemin Ku
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Abstract

Background: A sub-analysis of the Korean population in the LIBERTY ASTHMA QUEST trial (NCT02414854) revealed that dupilumab effectively treated severe uncontrolled asthma. This study aimed to assess the cost-effectiveness of add-on therapy with dupilumab to background therapy in patients ≥ 12 years of age with uncontrolled severe asthma compared to that of background therapy in South Korea.

Methods: The cost-effectiveness analysis was conducted using a Markov model over a lifetime from the Korean healthcare system perspective. Clinical efficacy and utility weights were obtained from post-hoc analyses of the Korean population in the QUEST trial. Data on the costs and treatment setting of exacerbation in a real-world setting were retrospectively collected using the administrative medical database from a single tertiary hospital.

Results: The base-case results indicated that add-on dupilumab therapy increases costs ($112,924 for add-on dupilumab versus $29,545 for background therapy alone). However, add-on dupilumab increased quality-adjusted life years (QALYs, 8.03 versus 3.93, respectively), with fewer events of severe exacerbations per patient compared to using the background therapy alone (17.920 versus 19.911, respectively). The incremental cost-effectiveness ratio was $20,325 per QALY. Various sensitivity analyses supported the robustness of the base-case results. Probabilistic sensitivity analysis showed that the probability of add-on dupilumab being cost-effective was 87% at a threshold willingness-to-pay of $26,718 (KRW 35 million) per QALY gained.

Conclusions: Dupilumab is cost-effective for adolescents and adults with uncontrolled severe asthma in South Korea. Our study provides evidence to support clinicians and policymakers in making informed decisions for severe asthma management.

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利用 LIBERTY ASTHMA QUEST 韩国数据,对未受控的重症哮喘患者进行杜必鲁单抗成本效益分析。
研究背景LIBERTY ASTHMA QUEST试验(NCT02414854)对韩国人群进行的子分析表明,dupilumab能有效治疗未受控制的重症哮喘。本研究旨在评估在韩国,与背景疗法相比,对年龄≥12岁的未受控重症哮喘患者在背景疗法基础上加用杜比单抗的成本效益:成本效益分析采用马尔可夫模型,从韩国医疗保健系统的角度对患者的一生进行分析。临床疗效和效用权重来自 QUEST 试验中韩国人群的事后分析。通过一家三级医院的行政医疗数据库回顾性收集了现实世界中病情加重的成本和治疗环境数据:基础研究结果表明,加用杜比单抗会增加成本(加用杜比单抗的成本为 112,924 美元,而单独使用背景疗法的成本为 29,545 美元)。然而,与单独使用背景疗法相比,附加双珠单抗疗法增加了质量调整生命年(QALYs,分别为 8.03 对 3.93),每位患者的严重病情加重事件也减少了(分别为 17.920 对 19.911)。每 QALY 的增量成本效益比为 20,325 美元。各种敏感性分析证实了基础病例结果的稳健性。概率敏感性分析表明,在每QALY收益26,718美元(3500万韩元)的支付意愿阈值下,附加杜比单抗具有成本效益的概率为87%:结论:在韩国,杜匹单抗对患有不受控制的重症哮喘的青少年和成人具有成本效益。我们的研究为临床医生和政策制定者在重症哮喘管理方面做出明智决策提供了证据支持。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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