PRECISIONheor, Los Angeles, CA.
Exact Sciences Corporation, Madison, WI.
J Manag Care Spec Pharm. 2021 May;27(5):650-659. doi: 10.18553/jmcp.2021.20471. Epub 2021 Mar 29.
U.S. value framework developers such as the Institute for Clinical and Economic Review (ICER) use cost-effectiveness analysis to value new health care technologies. Often, these value assessment frameworks use a health system perspective without fully accounting for societal and broader benefits and costs of an intervention. Although there is ongoing debate about the most appropriate methods for including broader value elements in value assessment, it remains unclear whether the inclusion of these value elements is likely to affect the quantitative estimates of treatment value. To assess variations in the relevance of broader value elements to cost-effectiveness analysis across diseases. Thirty-two broader value elements (e.g., caregiver burden, health equity, real option value, productivity) not traditionally included in health technology assessments were identified through a targeted literature review. Evidence reports published by ICER between July 2017 and January 2020 were evaluated to identify which broader value elements were discussed as relevant to each disease in the report text. The study examined whether there were associations among ICER's discussion of broader value elements, rare disease status, treatment cost, estimated treatment cost-effectiveness, and ICER committee voting results for contextual considerations and additional benefits/disadvantages. The most commonly cited broader value element category in the ICER evidence reports was household and leisure (e.g., absenteeism from normal activities and caregiver burden). More value elements were cited for inherited retinal disease (19 elements) and sickle cell disease (18 elements) than for other diseases. Cardiovascular disease and diabetes had the fewest number of value elements cited (7 elements). Rare diseases were more likely to have broader value elements cited compared with nonrare diseases (15.9 vs. 11.5, < 0.001). Treatments with higher (i.e., less favorable) incremental cost-effectiveness ratios were more likely to have a greater number of broader value elements cited ( = 0.625, < 0.001). The presence of broader value elements varied across diseases, with less cost-effective treatments more likely to have a higher number of relevant broader value elements. Inclusion of all relevant value elements in value assessments will more appropriately incentivize innovation and improve allocation of research funding. This study was sponsored by Novartis Pharmaceutical Corporation. At the time of this study, Shafrin was employed by PRECISIONheor, a consultancy to the life sciences industry that received financial support from Novartis to conduct this study. Dennen, Pednekar, and Birch are employed by PRECISIONheor. Bhor was an employee of Novartis Pharmaceutical Corporation at the time this research was conducted and manuscript was developed and reports grants from Novartis, unrelated to this work. Kanter has served on scientific advisory boards and steering committees for and reports receiving consulting fees from Novartis Pharmaceutical Corporation and is a site principal investigator on studies funded by Novartis Pharmaceutical Corporation. Kantar also reports support from Sickle Cell Disease Association of America Inc. and National Heart, Lung, and Blood Institute, unrelated to this work. Neumann reports advisory boards or consulting fees from Novartis Pharmaceutical Corporation and PRECISIONheor, as well as advisory boards or consulting fees unrelated to this study from AbbVie, Amgen, Avexis, Bayer, Congressional Budget Office, Janssen, Merck, Novartis, Novo Nordisk, Precision Health Economics, Veritech, Vertex; funding from The CEA Registry Sponsors by various pharmaceutical and medical device companies; and grants from Amgen, Lundbeck, Bill and Melinda Gates Foundation, National Pharmaceutical Council, Alzheimer's Association, and the National Institutes for Health.
美国价值框架的开发者,如临床和经济审查学会(ICER),使用成本效益分析来评估新的医疗保健技术。这些价值评估框架通常采用卫生系统的视角,而没有充分考虑干预措施对社会和更广泛的利益和成本的影响。尽管对于在价值评估中纳入更广泛的价值要素的最合适方法存在持续的争论,但仍不清楚纳入这些价值要素是否会影响治疗价值的定量估计。评估更广泛的价值要素在疾病间成本效益分析中的相关性的变化。通过有针对性的文献综述,确定了 32 个传统上未纳入卫生技术评估的更广泛的价值要素(例如,照顾者负担、卫生公平、实物期权价值、生产力)。评估了 2017 年 7 月至 2020 年 1 月期间 ICER 发布的证据报告,以确定报告文本中讨论了哪些更广泛的价值要素与每种疾病相关。本研究考察了 ICER 对更广泛价值要素的讨论、罕见病状态、治疗成本、估计治疗成本效益以及 ICER 委员会投票结果之间是否存在关联,这些投票结果涉及背景考虑因素和额外的利弊。ICER 证据报告中最常引用的更广泛价值要素类别是家庭和休闲(例如,正常活动缺勤和照顾者负担)。遗传性视网膜疾病(19 个要素)和镰状细胞病(18 个要素)比其他疾病引用的价值要素更多。心血管疾病和糖尿病引用的价值要素最少(7 个)。与非罕见疾病相比,罕见疾病更有可能引用更广泛的价值要素(15.9 比 11.5,<0.001)。成本效益比(即,不太有利)较高的治疗方法更有可能引用更多的更广泛的价值要素(=0.625,<0.001)。更广泛的价值要素在疾病之间存在差异,成本效益较低的治疗方法更有可能引用更多相关的更广泛的价值要素。在价值评估中纳入所有相关的价值要素将更适当地激励创新,并改善研究资金的分配。本研究由诺华制药公司赞助。在本研究进行时,Shafrin 受雇于 PRECISIONheor,这是一家为生命科学行业提供咨询服务的公司,从诺华制药公司获得资金支持进行这项研究。Dennen、Pednekar 和 Birch 受雇于 PRECISIONheor。Bhor 在进行这项研究时是诺华制药公司的员工,该研究开发了一份手稿,并报告了诺华制药公司的拨款,与这项工作无关。Kanter 曾担任 Novartis Pharmaceutical Corporation 的科学顾问委员会和指导委员会成员,并报告收取咨询费,是 Novartis Pharmaceutical Corporation 资助的研究的主要研究者。Kanter 还报告说,他得到了 Sickle Cell Disease Association of America Inc. 和 National Heart、Lung、and Blood Institute 的支持,与这项工作无关。Neumann 报告说,他在 Novartis Pharmaceutical Corporation 和 PRECISIONheor 担任顾问委员会或咨询委员会成员,以及在 AbbVie、Amgen、Avexis、Bayer、Congressional Budget Office、Janssen、Merck、Novartis、Novo Nordisk、Precision Health Economics、Veritech、Vertex 担任顾问委员会或咨询委员会成员,以及在与这项研究无关的其他公司担任顾问委员会或咨询委员会成员,这些公司包括 Amgen、Lundbeck、Bill and Melinda Gates Foundation、National Pharmaceutical Council、Alzheimer's Association 和 National Institutes for Health。