Langley Paul C
Adjunct Professor, College of Pharmacy, University of Minnesota.
Innov Pharm. 2019 Oct 31;10(4). doi: 10.24926/iip.v10i4.2337. eCollection 2019.
Previous commentaries in the Formulary Evaluation section of INNOVATIONS in Pharmacy have pointed to the lack of credibility in modeled claims for cost-effectiveness and associated recommendations for pricing by the Institute for Clinical and Economic Review (ICER). The principal objection to ICER reports has been that their modeled claims fail the standards of normal science: they are best seen as pseudoscience. The purpose of this latest commentary is to consider the recently released ICER report for Additive Cardiovascular Disease therapies. This report should not be taken seriously in its claims for cost-effectiveness and pricing in cardiovascular disease (CVD). The analytical framework applied by ICER fails to meet the standards of normal science in demarcating science from pseudoscience. Irrespective of the value judgements and recommendations of an ICER report, these lack credibility. They were never intended to be evaluable and replicable across treatment settings. The claims made are constructed, driven by assumption, and should be put to one side by health system decision makers. In this review the focus is on to the ICER modeled estimates of utility scores in CVD, the insistence on utilizing a generic utility algorithm (the EQ-5D-3L) and the consequent quality adjusted life year (QALY) estimates. Two issues are raised that will be the subject of future commentaries: the lack of appreciation of fundamental measurement and (ii) the importance of the patient voice in benefit claims. Given the importance in the ICER methodology of QALYS, the ad hoc nature of the ordinal utilities introduced to the cardiovascular model must raise concerns over the role the ICER evidence report may play in health care decision-making. These concerns extend to the claim by ICER that, on ICER's own affordability threshold for individual new molecular entities, the anticipated uptake of these therapies may raise questions of overall affordability. Again, we are dealing with an arbitraryconstruct that may adversely impact patient access.
《药学创新》“处方集评估”板块之前的评论指出,临床与经济评论研究所(ICER)在成本效益的模型化声明以及相关定价建议方面缺乏可信度。对ICER报告的主要反对意见是,其模型化声明未达到常规科学的标准:它们最好被视为伪科学。这篇最新评论的目的是审视ICER最近发布的关于心血管疾病附加疗法的报告。该报告在心血管疾病(CVD)成本效益和定价方面的声明不应被当真。ICER应用的分析框架在区分科学与伪科学方面未达到常规科学的标准。无论ICER报告的价值判断和建议如何,这些都缺乏可信度。它们从未打算在不同治疗环境中可评估和可复制。所做的声明是基于假设构建的,卫生系统决策者应将其搁置一旁。在本综述中,重点关注ICER对CVD效用评分的模型化估计、坚持使用通用效用算法(EQ - 5D - 3L)以及由此得出的质量调整生命年(QALY)估计。提出了两个问题,将成为未来评论的主题:一是对基本测量缺乏认识,二是患者声音在效益声明中的重要性。鉴于QALYs在ICER方法中的重要性,引入心血管模型的序数效用的临时性质必然引发对ICER证据报告在医疗保健决策中可能发挥的作用的担忧。这些担忧还延伸至ICER声称,就ICER自身对单个新分子实体的可承受性阈值而言,这些疗法的预期采用可能引发整体可承受性的问题。同样,我们面对的是一个可能对患者获得治疗产生不利影响的任意构建。