Ramos Mafalda, Haughney John, Henry Nathaniel, Lindner Leandro, Lamotte Mark
Real World Evidence, IMS Health, Zaventem, Belgium.
Academic Primary Care Division of Applied Health Sciences, University of Aberdeen, Aberdeen, Scotland.
Clinicoecon Outcomes Res. 2016 Sep 12;8:445-56. doi: 10.2147/CEOR.S107121. eCollection 2016.
Aclidinium-formoterol 400/12 µg is a long-acting muscarinic antagonist (LAMA) and a long-acting β2-agonist in a fixed-dose combination used in the management of patients with COPD. This study aimed to assess the cost-effectiveness of aclidinium-formoterol 400/12 µg against the long-acting muscarinic antagonist aclidinium bromide 400 µg.
A five-health-state Markov transition model with monthly cycles was developed using MS Excel to simulate patients with moderate-to-severe COPD and their initial lung-function improvement following treatment with aclidinium-formoterol 400/12 µg or aclidinium 400 µg. Health states were based on severity levels defined by Global Initiative for Chronic Obstructive Lung Disease 2010 criteria. The analysis was a head-to-head comparison without step-up therapy, from the NHS Scotland perspective, over a 5-year time horizon. Clinical data on initial lung-function improvement were provided by a pooled analysis of the ACLIFORM and AUGMENT trials. Management, event costs, and utilities were health state-specific. Costs and effects were discounted at an annual rate of 3.5%. The outcome of the analysis was expressed as cost (UK£) per quality-adjusted life-year (QALY) gained. The analysis included one way and probabilistic sensitivity analyses to investigate the impact of parameter uncertainty on model outputs.
Aclidinium-formoterol 400/12 µg provided marginally higher costs (£41) and more QALYs (0.014), resulting in an incremental cost-effectiveness ratio of £2,976/QALY. Sensitivity analyses indicated that results were robust to key parameter variations, and the main drivers were: mean baseline forced expiratory volume in 1 second (FEV1), risk of exacerbation, FEV1 improvement from aclidinium-formoterol 400/12 µg, and lung-function decline. The probability of aclidinium-formoterol 400/12 µg being cost-effective (using a willingness-to-pay threshold of £20,000/QALY) versus aclidinium 400 µg was 79%.
In Scotland, aclidinium-formoterol 400/12 µg can be considered a cost-effective treatment option compared to aclidinium 400 µg alone in patients with moderate-to-severe COPD.
阿地溴铵-福莫特罗400/12微克是一种长效毒蕈碱拮抗剂(LAMA)和长效β2受体激动剂的固定剂量组合,用于慢性阻塞性肺疾病(COPD)患者的管理。本研究旨在评估阿地溴铵-福莫特罗400/12微克相对于长效毒蕈碱拮抗剂阿地溴铵400微克的成本效益。
使用MS Excel开发了一个具有每月周期的五健康状态马尔可夫转换模型,以模拟中重度COPD患者以及使用阿地溴铵-福莫特罗400/12微克或阿地溴铵400微克治疗后的初始肺功能改善情况。健康状态基于慢性阻塞性肺疾病全球倡议2010标准定义的严重程度级别。该分析是从苏格兰国民保健服务(NHS)的角度进行的头对头比较,不采用逐步升级治疗,时间跨度为5年。初始肺功能改善的临床数据由ACLIFORM和AUGMENT试验的汇总分析提供。管理、事件成本和效用因健康状态而异。成本和效果按每年3.5%的比率进行贴现。分析结果以每获得一个质量调整生命年(QALY)的成本(英镑)表示。该分析包括单因素和概率敏感性分析,以研究参数不确定性对模型输出的影响。
阿地溴铵-福莫特罗400/12微克的成本略高(41英镑),获得的QALY更多(0.014),导致增量成本效益比为2976英镑/QALY。敏感性分析表明,结果对关键参数变化具有稳健性,主要驱动因素包括:1秒用力呼气容积(FEV1)的平均基线值、急性加重风险、阿地溴铵-福莫特罗400/12微克导致的FEV1改善以及肺功能下降。与阿地溴铵400微克相比,阿地溴铵-福莫特罗40/12微克具有成本效益(采用20000英镑/QALY的支付意愿阈值)的概率为79%。
在苏格兰,与单独使用阿地溴铵400微克相比,对于中重度COPD患者,阿地溴铵-福莫特罗400/12微克可被视为一种具有成本效益的治疗选择。