Cost-effectiveness analysis of secukinumab versus standard of care in the treatment of psoriatic arthritis: A Vietnam National health insurance perspective

Nguyen Thi Mai Phuong, Hua Thanh Thuy, Ong The Due, Phung Lam Toi, Do Thi Thu Hien, Nguyen Van Thanh, Vuong Trong Hieu, Pham Nu Hanh Van
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Abstract

Psoriatic arthritis (PsA) is a chronic, systemic inflammatory disease. This study assessed the cost-effectiveness of secukinumab, an interleukin-17A inhibitor, versus standard of care (SoC) from Vietnam’s National Health Insurance (NHI) perspective. Model-based cost-effectiveness analysis, the structure was a 3-month decision tree leading into a Markov model. Clinical parameters, including responses at 3 months, were from the FUTURE 2 trial. Cost parameters were from real data at the National Hospital of Dermatology and Venereology and a research period. The outcome included total costs and quality-adjusted life years (QALYs) over a life-time horizon (3.5% annual discount for both outcomes and cost), and incremental cost-effectiveness ratios (ICER). The robustness of the study findings was evaluated via sensitivity analysis. Patients treated with secukinumab achieved with QALY gain 1.16 versus SoC, but associated with higher total costs was 211.3 million VND over lifetime horizon. ICER for secukinumab vs SoC was 181.6 million VND lower than a willingness to pay threshold recommended in Vietnam (3GDP per capita equal to 286.8 million VND). Deterministic sensitivity analysis indicated that parameters related to Health Assessment Questionnaire scores were most influential. At the willingness to pay threshold of three times the GDPpc, the probability of secukinumab being cost-effective was 90.3% in the probabilistic sensitivity analysis. Secukinumab is a cost-effectiveness treatment versus SoC for PsA patients from the National health insurance’s perspective of Vietnam.
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secukinumab与标准疗法治疗银屑病关节炎的成本效益分析:越南国家医疗保险的视角
银屑病关节炎(PsA)是一种慢性、全身性炎症性疾病。本研究从越南国家医疗保险(NHI)的角度评估了白细胞介素-17A抑制剂secukinumab与标准治疗(SoC)的成本效益。基于模型的成本效益分析,其结构是一个 3 个月的决策树,然后进入马尔可夫模型。临床参数(包括 3 个月的反应)来自 FUTURE 2 试验。成本参数来自国立皮肤病与性病医院的真实数据和研究期间的数据。结果包括总成本、终生质量调整生命年(QALYs)(结果和成本的年贴现率均为 3.5%)以及增量成本效益比(ICER)。研究结果的稳健性通过敏感性分析进行了评估。与SoC相比,接受secukinumab治疗的患者获得的QALY收益为1.16,但在终生范围内的相关总成本较高,为2.113亿越南盾。secukinumab与SoC相比的ICER为1.816亿越南盾,低于越南建议的支付意愿阈值(人均3GDP等于2.868亿越南盾)。确定性敏感性分析表明,与健康评估问卷得分相关的参数影响最大。在支付意愿阈值为 GDPpc 三倍的情况下,在概率敏感性分析中,secukinumab 具有成本效益的概率为 90.3%。从越南国家医疗保险的角度来看,Secukinumab 对 PsA 患者的治疗与 SoC 相比具有成本效益。
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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