University of Helsinki, Helsinki, Finland.
ESiOR Oy, Kuopio, Finland.
PLoS One. 2019 Jul 24;14(7):e0220142. doi: 10.1371/journal.pone.0220142. eCollection 2019.
The objective of this study was to evaluate the cost-effectiveness of abatacept, tocilizumab, and tumor necrosis factor (TNF) inhibitors as compared with rituximab in Finnish rheumatoid arthritis patients, who have previously been treated with TNF inhibitors.
A patient-level simulation model was developed to predict costs and outcomes associated with four biological drugs (abatacept, tocilizumab, rituximab and TNF inhibitors) in the treatment of rheumatoid arthritis. Following lack of efficacy or adverse events, the patients were switched to another biological drug until all four options were exhausted. After that, the patients were assumed to receive a 6th line treatment until death. The patients' baseline characteristics and regression models used in the simulation were based on observational data from the National Register for Biological Treatments in Finland. Direct costs comprised drug costs, administration costs, costs of switching, and outpatient and inpatient care, while indirect costs included disability pension and sick leaves due to rheumatoid arthritis. Several subgroup and deterministic sensitivity analyses were conducted.
Drug costs were the lowest for rituximab, but when administration costs and costs of switching were included, drug costs were the lowest for TNF inhibitors. Abatacept was associated with the highest drug costs, whereas rituximab was associated with the highest healthcare costs. In total, TNF inhibitors had the lowest direct costs, while rituximab had the highest direct costs. The amount of quality-adjusted life years (QALY) gained ranged from 9.405 for rituximab to 9.661 for TNF inhibitors. TNF inhibitors, abatacept, and tocilizumab were dominant in comparison to RTX.
TNF inhibitors, abatacept, and tocilizumab had lower costs and higher QALYs than rituximab, and therefore, they were dominant in comparison to rituximab. As TNF inhibitors had the lowest costs and highest QALYs, they were the most cost-effective treatment option.
本研究旨在评估阿巴西普、托珠单抗和肿瘤坏死因子(TNF)抑制剂与利妥昔单抗相比,在先前接受 TNF 抑制剂治疗的芬兰类风湿关节炎患者中的成本效益。
开发了一个患者水平的模拟模型,以预测四种生物药物(阿巴西普、托珠单抗、利妥昔单抗和 TNF 抑制剂)治疗类风湿关节炎的成本和结果。在疗效不佳或出现不良反应后,患者被转换为另一种生物药物,直到所有四种药物都用尽。之后,假设患者接受第六线治疗,直到死亡。患者的基线特征和模拟中使用的回归模型基于芬兰国家生物治疗登记处的观察性数据。直接成本包括药物成本、管理成本、转换成本以及门诊和住院护理费用,而间接成本包括因类风湿关节炎而导致的残疾抚恤金和病假。进行了几项亚组和确定性敏感性分析。
利妥昔单抗的药物成本最低,但当包括管理成本和转换成本时,TNF 抑制剂的药物成本最低。阿巴西普的药物成本最高,而利妥昔单抗的医疗保健成本最高。总的来说,TNF 抑制剂的直接成本最低,而利妥昔单抗的直接成本最高。获得的质量调整生命年(QALY)数量从利妥昔单抗的 9.405 到 TNF 抑制剂的 9.661。与 RTX 相比,TNF 抑制剂、阿巴西普和托珠单抗具有成本优势。
与利妥昔单抗相比,TNF 抑制剂、阿巴西普和托珠单抗的成本更低,QALYs 更高,因此与利妥昔单抗相比具有优势。由于 TNF 抑制剂的成本最低,QALYs 最高,因此是最具成本效益的治疗选择。