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新药评估机构(ICER)审查流程的演变及对经济评估的批判性回顾(2018-2019 年):利益相关方如何与新药评估机构合作,以提高新药评估机构报告中证据质量。

The evolution of ICER's review process for new medical interventions and a critical review of economic evaluations (2018-2019): how stakeholders can collaborate with ICER to improve the quality of evidence in ICER's reports.

机构信息

RTI Health Solutions, Research Triangle, NC.

出版信息

J Manag Care Spec Pharm. 2021 Nov;27(11):1601-1612. doi: 10.18553/jmcp.2021.27.11.1601.

Abstract

Since its inception in 2006, the Institute for Clinical and Economic Review (ICER) has rapidly gained influence on drug pricing and reimbursement decisions despite historical resistance to the use of cost-effectiveness thresholds in the US health care system. Although patient groups, physicians, and pharmaceutical manufacturers voiced their concerns about the potential negative effects of increased use of ICER's assessments on patient access to innovative medications, there is little guidance and consensus on how the stakeholders should collaborate with ICER to ensure that its reviews reflect the best clinical and economic evidence. To (1) summarize the evolution of ICER's evaluation procedure, scope, and topics; (2) evaluate the effectiveness of stakeholder engagement approaches; and (3) inform stakeholders of their potential role in collaborating with ICER in estimating the cost-effectiveness of new interventions. Publicly available ICER evaluations from 2008 to 2019 were systematically reviewed. Changes in evaluation procedures, scope, and topics were summarized. For evaluations that occurred in 2018 (n = 12) and 2019 (n = 8), key characteristics were extracted from 172 letters documenting interactions between ICER and all stakeholders who provided comments to draft reports. Stakeholder suggestions were analyzed in terms of their effectiveness indicated by ICER's reconsideration of its original cost-effectiveness analysis approach. The number of ICER evaluations increased consistently from 2 to 12 per year between 2008 and 2018 but declined to 8 in 2019. Stakeholder opportunity to engage with ICER increased from 1 to 3 per evaluation between 2008 and 2015. ICER initially focused on reviewing general treatment strategies but shifted its focus to specific pharmaceuticals and medical devices in 2014. In 2018 and 2019, 30% of 172 stakeholder letters resulted in a revision in the base-case analysis (49 comments in 2018, 23 in 2019); nearly half of comments in these letters included specific alternative data or a published article to rationalize recommendations. Other common types of suggestions that resulted in ICER's base-case analysis revisions included comments relating to inconsistent methods used to derive model inputs across different treatments (12/49 in 2018, 5/23 in 2019); clinical justifications (12/49 in 2018, 0/23 in 2019); and justifications based on patient perspectives (1/49 in 2018, 5/23 in 2019). These revisions rarely affected ICER's conclusions on the cost-effectiveness of evaluated interventions. Among the 20 assessments that involved 172 stakeholder engagements in 2018 and 2019, only 2% (n = 3) of the engagements (all from 2018) were associated with a change in the cost-effectiveness conclusion. Between 2018 and 2019, stakeholders leveraged ICER evaluations as opportunities to promote dialogue for better understanding of the value of technologies. Actionable, evidence-based recommendations were accepted more often than other recommendations. No outside funding supported this study. The authors have no conflicts of interest to disclose. Findings from this study were presented as a poster at Virtual ISPOR, May 17-20, 2021.

摘要

自 2006 年成立以来,尽管美国医疗保健系统历史上一直抵制使用成本效益阈值,但临床与经济评价研究所(ICER)在药品定价和报销决策方面迅速获得了影响力。尽管患者群体、医生和制药制造商对增加使用 ICER 评估对患者获得创新药物的潜在负面影响表示担忧,但对于利益相关者应如何与 ICER 合作以确保其评估反映最佳临床和经济证据,几乎没有指导意见和共识。(1)总结 ICER 评估程序、范围和主题的演变;(2)评估利益相关者参与方法的有效性;(3)告知利益相关者在估计新干预措施的成本效益方面与 ICER 合作的潜在作用。系统回顾了 2008 年至 2019 年公开的 ICER 评估。总结了评估程序、范围和主题的变化。对于 2018 年(n=12)和 2019 年(n=8)发生的评估,从记录 ICER 与所有提供报告草稿意见的利益相关者之间互动的 172 封信中提取了关键特征。根据 ICER 重新考虑其原始成本效益分析方法的有效性,分析了利益相关者的建议。2008 年至 2018 年,ICER 的评估数量从每年 2 项稳步增加到 12 项,但在 2019 年下降到 8 项。利益相关者与 ICER 互动的机会从 2008 年至 2015 年的每年 1 次增加到 3 次。ICER 最初专注于审查一般治疗策略,但在 2014 年将重点转移到特定的药品和医疗器械上。在 2018 年和 2019 年,172 封利益相关者信件中有 30%(49 封 2018 年,23 封 2019 年)导致基础分析的修订;这些信件中的近一半意见包括特定的替代数据或已发表的文章,以合理化建议。导致 ICER 基础案例分析修订的其他常见建议类型包括与不同治疗方法中模型输入的推导方法不一致有关的意见(2018 年 12/49,2019 年 5/23);临床理由(2018 年 12/49,2019 年 0/23);以及基于患者观点的理由(2018 年 1/49,2019 年 5/23)。这些修订很少影响 ICER 对评估干预措施成本效益的结论。在 2018 年和 2019 年涉及 172 次利益相关者参与的 20 项评估中,只有 2%(n=3)的参与(均来自 2018 年)与成本效益结论的改变有关。2018 年至 2019 年,利益相关者利用 ICER 评估作为促进对话以更好地了解技术价值的机会。可操作的、基于证据的建议比其他建议更常被接受。本研究没有外部资金支持。作者没有利益冲突需要披露。本研究的结果作为海报在 2021 年 5 月 17 日至 20 日的虚拟 ISPOR 上展示。

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