Sequential biologic therapy in the treatment of active psoriatic arthritis in China: a cost-effectiveness analysis.

IF 2.8 3区 医学 Q2 RHEUMATOLOGY Clinical Rheumatology Pub Date : 2025-04-01 Epub Date: 2025-02-21 DOI:10.1007/s10067-025-07368-1
Ouyang Xie, Meiyu Wu, Andong Li, Kehui Meng, Heng Xiang, Chongqing Tan, Liubao Peng, Yan Ge, Xiaomin Wan
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Abstract

Objective: Compared with conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), biologics are more effective and are recommended to be included in the sequential treatment for psoriatic arthritis (PsA) patients. However, biologics are expensive and the cost-effectiveness of sequential biologic therapy in China remains unknown. The purpose of this study is to evaluate the cost-effectiveness of different sequential treatment option for PsA patients who have not responded to csDMARDs from the perspective of Chinese healthcare system.

Methods: We constructed a discrete event simulation model to evaluate the cost-effectiveness of 7 monotherapy treatments and 32 sequential treatments. In sequential therapy, two different types of biologics were used as first-line and second-line treatments, respectively, with the best supportive care (BSC) as the third-line treatment. The primary outcomes included total treatment costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs). One-way and probability sensitivity analyses were performed to explore the uncertainty of our model.

Results: Compared to all other strategies, initiating with secukinumab followed by etanercept (SEC-ETN) provided the highest health benefits. At a willingness-to-pay (WTP) threshold of US $38,161 per QALY, SEC-ETN was the most cost-effective strategy, with an ICER of $20,837 per QALY. One-way sensitivity analysis and probabilistic sensitivity analysis results confirmed the robust of this conclusion.

Conclusions: In China, SEC-ETN may be the most cost-effective strategy for patients who have failed treatment with csDMARDs and have not previously used biologics. The results provide evidence for identifying the optimal biologic treatment strategy for PsA patients in China. Key Points • Compared with conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), biologics are more effective and are recommended to be included in the sequential treatment for psoriatic arthritis (PsA) patients. However, the cost-effectiveness of sequential biologic therapy in China remains unclear. • At a willingness-to-pay threshold of $38,161, initiating with secukinumab followed by etanercept (SEC-ETN) was cost-effective strategy, outperforming other strategies. • From the perspective of the Chinese healthcare system, the optimal biologic treatment strategy was SEC-ETN in China.

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序贯生物疗法治疗中国活动性银屑病关节炎:成本-效果分析。
目的:与传统的合成疾病缓解抗风湿药物(csDMARDs)相比,生物制剂更有效,推荐纳入银屑病关节炎(PsA)患者的序贯治疗。然而,生物制剂价格昂贵,序贯生物治疗的成本效益在中国尚不清楚。本研究的目的是从中国医疗体系的角度,评估不同序贯治疗方案对csdmard无应答的PsA患者的成本-效果。方法:构建离散事件模拟模型,评价7种单药治疗和32种序贯治疗的成本-效果。在序贯治疗中,分别采用两种不同类型的生物制剂作为一线和二线治疗,最佳支持治疗(BSC)作为三线治疗。主要结局包括总治疗费用、质量调整生命年(QALYs)和增量成本-效果比(ICERs)。采用单向和概率敏感性分析来探讨模型的不确定性。结果:与所有其他策略相比,首先使用secukinumab,然后使用依那西普(SEC-ETN)提供了最高的健康益处。在每个QALY 38,161美元的支付意愿(WTP)门槛下,SEC-ETN是最具成本效益的策略,每个QALY的ICER为20,837美元。单因素敏感性分析和概率敏感性分析结果证实了这一结论的稳健性。结论:在中国,对于csdmard治疗失败且以前未使用过生物制剂的患者,SEC-ETN可能是最具成本效益的策略。结果为确定中国PsA患者的最佳生物治疗策略提供了依据。•与传统的合成疾病缓解抗风湿药物(csDMARDs)相比,生物制剂更有效,建议将其纳入银屑病关节炎(PsA)患者的序贯治疗。然而,序贯生物治疗的成本效益在中国尚不清楚。•在38161美元的支付意愿阈值下,首先使用secukinumab,然后使用依那西普(SEC-ETN)是一种具有成本效益的策略,优于其他策略。•从中国医疗系统的角度来看,中国最佳的生物治疗策略是SEC-ETN。
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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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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