Punekar Yogesh Suresh, Roberts Graeme, Ismaila Afisi, O'Leary Martin
Value Evidence and Outcomes, GlaxoSmithKline R&D, Stockley Park, Uxbridge, UB11 1BT UK.
Double Helix Consulting, London, W1U 6TQ UK.
Cost Eff Resour Alloc. 2015 Dec 12;13:22. doi: 10.1186/s12962-015-0048-6. eCollection 2015.
The cost-effectiveness of umeclidinium bromide-vilanterol (UMEC/VI) versus tiotropium monotherapy in the UK was assessed using a UMEC/VI treatment-specific economic model based on a chronic obstructive pulmonary disease (COPD) disease-progression model.
The model was implemented as a linked-equation model to estimate COPD progression and associated health service costs, and its impact on quality-adjusted life years (QALYs) and survival. Statistical risk equations for clinical endpoints and resource use were derived from the ECLIPSE and TORCH studies, respectively. For the selected timeframe (1-40 years) and probabilistic analysis, model outputs included disaggregated costs, total costs, exacerbations, life-years and QALYs gained, and incremental cost-effectiveness ratios (ICERs).
Random-effects meta-analysis of tiotropium comparator trials estimated treatment effect of UMEC/VI as 92.17 mL (95 % confidence interval: 61.52, 122.82) in forced expiratory volume in 1 s. With this benefit, UMEC/VI resulted in an estimated annual exacerbation reduction of 0.04 exacerbations/patient and 0.36 life years gained compared to tiotropium over patient lifetime. With an additional 0.18 QALYs/patient and an additional lifetime cost of £372/patient at price parity, the incremental cost effectiveness ratio (ICER) of UMEC/VI compared to tiotropium was £2088/QALY. This ICER increased to £17,541/QALY when price of UMEC/VI was increased to that of indacaterol plus tiotropium in separate inhalers. The ICER improved when model duration was reduced from patient lifetime to 1 or 5 years, or when treatment effect was assumed to last for 12 months following treatment initiation.
UMEC/VI can be considered a cost-effective alternative to tiotropium at a certain price.
基于慢性阻塞性肺疾病(COPD)疾病进展模型,使用乌美溴铵-维兰特罗(UMEC/VI)治疗特异性经济模型评估了UMEC/VI与噻托溴铵单药治疗在英国的成本效益。
该模型作为一个联立方程模型实施,以估计COPD进展及相关医疗服务成本,及其对质量调整生命年(QALYs)和生存率的影响。临床终点和资源使用的统计风险方程分别源自ECLIPSE和TORCH研究。对于选定的时间范围(1 - 40年)和概率分析,模型输出包括分解成本、总成本、急性加重次数、获得的生命年和QALYs以及增量成本效益比(ICERs)。
噻托溴铵对照试验的随机效应荟萃分析估计,UMEC/VI在1秒用力呼气容积方面的治疗效果为92.17 mL(95%置信区间:61.52,122.82)。有了这一益处,与噻托溴铵相比,UMEC/VI估计每年可使每位患者的急性加重次数减少0.04次,患者一生中可多获得0.36个生命年。在价格平价的情况下,每位患者额外增加0.18个QALYs且终身成本额外增加372英镑,UMEC/VI与噻托溴铵相比的增量成本效益比(ICER)为2088英镑/QALY。当UMEC/VI的价格提高到与茚达特罗加噻托溴铵单独吸入器的价格相同时,该ICER增加到17541英镑/QALY。当模型持续时间从患者终身缩短至1年或5年,或假设治疗效果在治疗开始后持续12个月时,ICER有所改善。
在一定价格下,UMEC/VI可被视为噻托溴铵具有成本效益的替代方案。