Value Evidence and Outcomes, GlaxoSmithKline plc., Brentford, UK.
Global Health Economics, ICON plc., Boston, MA, USA.
Int J Chron Obstruct Pulmon Dis. 2020 Jul 10;15:1621-1632. doi: 10.2147/COPD.S240556. eCollection 2020.
To evaluate the cost-effectiveness of once-daily fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) vs twice-daily budesonide/formoterol (BUD/FOR) in patients with symptomatic chronic obstructive pulmonary disease (COPD) at risk of exacerbations, from the Spanish National Healthcare System perspective.
The validated GALAXY-COPD model was used to simulate disease progression and predict healthcare costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs) over a 3-year time horizon for a Spanish population. Patient characteristics from published literature were supplemented by data from FULFIL (NCT02345161), which compared FF/UMEC/VI vs BUD/FOR in patients with symptomatic COPD at risk of exacerbations. Treatment effects, extrapolated to 3 years, were based on Week 24 results in the FULFIL intent-to-treat population, including change in forced expiratory volume in 1 second, St. George's Respiratory Questionnaire score, and exacerbation rates. Treatment, exacerbations, and COPD management costs (2019€) were informed by Spanish public sources and published literature. A 3% discount rate for costs and benefits was applied. One-way sensitivity and scenario analyses, and probabilistic sensitivity analysis (PSA), were performed.
FF/UMEC/VI treatment led to fewer moderate and severe exacerbations (2.126 and 0.306, respectively) vs BUD/FOR (2.608 and 0.515, respectively), with a mean incremental cost of €69 and gain of 0.107 QALYs, which resulted in an ICER of €642 per QALY gained. In sensitivity analyses, the ICER was most sensitive to treatment effect variations in exacerbations and healthcare resource utilization/event costs. Overall, 95% of 1000 PSA simulations resulted in an ICER less than €11,000 per QALY gained for FF/UMEC/VI vs BUD/FOR, confirming robustness of the results. The probability of FF/UMEC/VI being cost-effective vs BUD/FOR was 100% at a willingness-to-pay threshold of €30,000 per QALY gained.
At the accepted Spanish ICER threshold of €30,000, FF/UMEC/VI represents a cost-effective treatment option vs BUD/FOR in patients with symptomatic COPD at risk of exacerbations.
从西班牙国家医疗保健系统的角度评估每日一次氟替卡松乌美溴铵/维兰特罗(FF/UMEC/VI)与每日两次布地奈德/福莫特罗(BUD/FOR)治疗有加重风险的症状性慢性阻塞性肺疾病(COPD)患者的成本效益。
使用经过验证的 GALAXY-COPD 模型来模拟疾病进展,并预测西班牙人群的医疗保健成本、质量调整生命年(QALY)和增量成本效益比(ICER),时间范围为 3 年。从已发表的文献中获取患者特征,并补充来自 FULFIL(NCT02345161)的数据,该研究比较了有加重风险的症状性 COPD 患者中 FF/UMEC/VI 与 BUD/FOR 的疗效。基于 FULFIL 意向治疗人群第 24 周的结果,将治疗效果外推至 3 年,包括第 1 秒用力呼气量的变化、圣乔治呼吸问卷评分和加重率。治疗、加重和 COPD 管理成本(2019 欧元)来自西班牙公共来源和已发表的文献。对成本和效益应用了 3%的贴现率。进行了单因素敏感性分析、情景分析和概率敏感性分析(PSA)。
与 BUD/FOR(分别为 2.608 和 0.515)相比,FF/UMEC/VI 治疗导致中度和重度加重的发生率更低(分别为 2.126 和 0.306),增量成本为 69 欧元,增加了 0.107 QALY,导致每获得一个 QALY 的 ICER 为 642 欧元。在敏感性分析中,ICER 对加重和医疗资源利用/事件成本的治疗效果变化最为敏感。总体而言,在 1000 次 PSA 模拟中,有 95%的模拟结果显示,与 BUD/FOR 相比,FF/UMEC/VI 每获得一个 QALY 的成本效益比低于 11000 欧元,这证实了结果的稳健性。在愿意支付每获得一个 QALY 30000 欧元的阈值下,FF/UMEC/VI 成为比 BUD/FOR 更具成本效益的治疗选择的概率为 100%。
在西班牙可接受的 ICER 阈值 30000 欧元下,与 BUD/FOR 相比,FF/UMEC/VI 是一种有加重风险的症状性 COPD 患者的成本效益治疗选择。