Cost-effectiveness analysis of subcutaneous biosimilar tocilizumab in patients with rheumatoid arthritis in Spain.

IF 1 Q4 PHARMACOLOGY & PHARMACY
Fernando Pérez-Ruiz, Carlos Crespo-Diz, Joan Antoni Schoenenberger-Arnaiz, Mónica Cerezales, Carlos Crespo, Marcelo Alejandro Guigini, José Ignacio Peinado-Fabregat, Mónica Climente-Martí
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引用次数: 0

Abstract

Introduction: Rheumatoid arthritis (RA) is the most common chronic inflammatory rheumatic disease, its management and morbidity impose a great burden to healthcare systems. Development and rollout of biological disease modifying anti-rheumatic drugs has contributed to improvements for patients, however, high costs have prevented them to be widely used. This is being addressed with biosimilars, with equal benefit-risk profile and reduced costs. The objective is to analyze the cost-effectiveness of subcutaneous biosimilar tocilizumab (bsTCZ) for patients with moderate-severe RA in Spain from a healthcare system perspective.

Methods: A Markov model was developed with a lifetime horizon including 5 health states: remission of the disease; low, moderate, or high activity; and death. A PICO-S-T search retrieved efficacy of treatments in meta-analysis and network meta-analysis, and was further complemented with published clinical trials. Pharmacological costs were obtained from the BotPlus database, and medical resources costs from regional tariffs. Deterministic and probabilistic sensitivity analysis were performed to validate the robustness of results. Incremental cost-effectiveness ratio (ICER) for cost/percentage of remission and cost/quality-adjusted life year (QALY) gain were calculated.

Results: Lifetime cost of bsTCZ was 183 741€ (lowest) versus comparative costs ranging from 184 317€ for infliximab to 201 972€ (highest) for certolizumab. QALYs were 13.74 for upadacitinib and 13.73 for sarilumab and tocilizumab with values between 13.53 and 13.72 for the comparators. ICERs as €/remission and €/QALY showed that bsTCZ was either dominant in most of the comparisons or the most cost-effective alternative. The sensitivity analysis showed that bsTCZ long term cost, and transition from low to moderate disease activity health status were the most influential factors. Moreover, bsTCZ was either dominant or cost-effective in all the comparisons.

Conclusions: bsTCZ demonstrated to be a cost-effective and cost-saving alternative for the treatment of patients with RA in Spain when compared to all the available therapeutic alternatives.

西班牙类风湿关节炎患者皮下生物仿制药tocilizumab的成本-效果分析
类风湿关节炎(RA)是最常见的慢性炎症性风湿性疾病,其管理和发病率给卫生保健系统带来了巨大负担。生物疾病修饰抗风湿药物的开发和推出有助于改善患者的病情,然而,高昂的成本阻碍了它们的广泛应用。生物仿制药可以解决这一问题,具有同等的收益-风险和更低的成本。目的是从医疗保健系统的角度分析西班牙中重度RA患者皮下生物仿制药tocilizumab (bsTCZ)的成本效益。方法:建立一个马尔可夫模型,包括5种健康状态:疾病缓解;运动:低、中等或高的活动;和死亡。PICO-S-T检索在荟萃分析和网络荟萃分析中检索了治疗的疗效,并进一步补充了已发表的临床试验。药理学费用来自BotPlus数据库,医疗资源费用来自区域关税。进行确定性和概率敏感性分析以验证结果的稳健性。计算成本/缓解百分比的增量成本-效果比(ICER)和成本/质量调整生命年(QALY)增益。结果:bsTCZ的终生成本为183 741欧元(最低),而英夫利昔单抗的终生成本为184 317欧元,certolizumab的终生成本为201 972欧元(最高)。upadacitinib的QALYs为13.74,sarilumab和tocilizumab的QALYs为13.73,比较药的QALYs在13.53和13.72之间。ICERs作为€/缓解和€/QALY表明bsTCZ在大多数比较中占主导地位,或者是最具成本效益的替代方案。敏感性分析显示,bsTCZ的长期成本和从低到中等疾病活动健康状态的转变是最重要的影响因素。此外,bsTCZ在所有比较中都具有优势或成本效益。结论:与所有可用的治疗方案相比,bsTCZ被证明是西班牙治疗RA患者的一种具有成本效益和节省成本的替代方案。
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来源期刊
FARMACIA HOSPITALARIA
FARMACIA HOSPITALARIA PHARMACOLOGY & PHARMACY-
CiteScore
1.90
自引率
21.40%
发文量
46
审稿时长
37 days
期刊介绍: Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.
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