Formerly of Evidera, London, UK.
Formerly of Sanofi, Guildford, UK.
Adv Ther. 2019 Jun;36(6):1337-1357. doi: 10.1007/s12325-019-00946-1. Epub 2019 Apr 19.
Assess the cost-effectiveness (US healthcare payer perspective) of sarilumab subcutaneous (SC) 200 mg + methotrexate versus conventional synthetic disease-modifying anti-rheumatic drugs (csDMARDs) or targeted DMARD + methotrexate for moderate-to-severe rheumatoid arthritis (RA) in adults with inadequate response to methotrexate.
Microsimulation based on patient profiles from MOBILITY (NCT01061736) was conducted via a 6-month decision tree and lifetime Markov model with 6-monthly cycles. Treatment response at 6 months was informed by a network meta-analysis and based on American College of Rheumatology (ACR) response. Responders: patients with ACR20 response who continued with therapy; non-responders: ACR20 non-responders who transitioned to the subsequent treatment. Utilities and quality-adjusted life-years (QALYs) were estimated via mapping 6-month ACR20/50/70 response to relative change in Health Assessment Questionnaire Disability Index score (short term) and based on published algorithms (long term). Direct costs considered drugs (wholesale acquisition costs), administration and routine care.
Lifetime QALYs and costs for treatment sequences on the efficiency frontier were 3.43 and $115,019 for active csDMARD, 5.79 and $430,918 for sarilumab, and 5.94 and $524,832 for etanercept (all others dominated). Sarilumab was cost-effective versus tocilizumab and csDMARD (incremental cost-effectiveness ratios of $84,079/QALY and $134,286/QALY). Probabilistic sensitivity analysis suggested comparable costs and slightly improved health benefits for sarilumab versus tocilizumab, irrespective of threshold.
In patients with moderate-to-severe RA, sarilumab 200 mg SC every 2 weeks + methotrexate can be considered a cost-effective treatment option, with lower costs and greater health benefits than alternative treatment sequences (+ methotrexate) beginning with adalimumab, certolizumab, golimumab and tofacitinib and below commonly accepted cost-effectiveness thresholds against tocilizumab + methotrexate or csDMARD active treatment.
Sanofi and Regeneron Pharmaceuticals, Inc.
评估sarilumab 皮下注射 200mg+甲氨蝶呤(SC+MTX)联合传统合成改善病情抗风湿药物(csDMARDs)或靶向 DMARD+MTX 治疗对接受 MTX 治疗后应答不足的中重度类风湿关节炎(RA)成人患者的成本效果(美国医保支付者视角)。
基于 MOBILITY (NCT01061736)患者特征的微观模拟,通过 6 个月决策树和终生 Markov 模型(每 6 个月一个周期)进行。6 个月时的治疗反应由网络荟萃分析提供信息,并根据美国风湿病学会(ACR)反应进行。应答者:达到 ACR20 反应的患者继续接受治疗;无应答者:未达到 ACR20 反应的患者过渡到后续治疗。通过将 6 个月 ACR20/50/70 反应映射到健康评估问卷残疾指数评分的相对变化来估计效用和质量调整生命年(QALY)(短期),并基于已发表的算法(长期)。直接成本考虑药物(批发采购成本)、管理和常规护理。
在效率前沿的治疗序列中,sarilumab 的终生 QALY 和成本分别为 3.43 和 115,019 美元,etanercept 为 5.79 和 430,918 美元,tocilizumab 为 5.94 和 524,832 美元(所有其他方案均被劣效)。与 tocilizumab 和 csDMARD 相比,sarilumab 具有成本效果(增量成本效果比分别为 84,079/QALY 和 134,286/QALY)。概率敏感性分析表明,sarilumab 与 tocilizumab 相比,成本相当,且健康获益略有改善,无论阈值如何。
在中重度 RA 患者中,sarilumab 200mg SC 每 2 周+MTX 可被视为一种具有成本效果的治疗选择,与起始用阿达木单抗、certolizumab、golimumab 和 tofacitinib 及以下的替代治疗方案(联合 MTX)相比,成本更低,健康获益更大,且低于针对 tocilizumab+MTX 或 csDMARD 活性治疗的常见可接受成本效果阈值。
赛诺菲和再生元制药公司。