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临床与经济评论学会的评估与德国联邦联合委员会的额外获益评估相比如何?一项定性研究。

How Do the Institute for Clinical and Economic Review's Assessments of Comparative Effectiveness Compare With the German Federal Joint Committee's Assessments of Added Benefit? A Qualitative Study.

机构信息

Center for Pharmaceutical Outcomes Research, Department of Clinical Pharmacy, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Institute for Clinical and Economic Review, Boston, MA, USA.

出版信息

Value Health. 2024 Aug;27(8):1066-1072. doi: 10.1016/j.jval.2024.04.015. Epub 2024 Apr 26.

DOI:10.1016/j.jval.2024.04.015
PMID:38679288
Abstract

OBJECTIVES

We compared the Institute for Clinical and Economic Review's (ICER) ratings of comparative clinical effectiveness with the German Federal Joint Committee's (G-BA) added benefit ratings, and explored what factors may explain the disagreement between the 2 organizations.

METHODS

We included drugs if they were assessed by ICER under its 2020 to 2023 Value Assessment Framework and had a corresponding assessment by G-BA as of January 2024 for the same indication, patient population, and comparator drug. To compare assessments, we modified ICER's proposed crosswalk between G-BA and ICER benefit ratings to account for G-BA's certainty ratings. We also determined whether each pair was based on similar evidence. Assessment pairs exhibiting disagreement based on the modified crosswalk despite a similar evidence base were qualitatively analyzed to identify reasons for disagreement.

RESULTS

Out of 15 drug assessment pairs matched on indication, patient subgroup, and comparator, none showed agreement in their assessments when based on similar evidence. Disagreement was attributed to differences in evidence evaluation, including evaluations of safety, generalizability, and study design, as well as G-BA's rejection of the available evidence in 4 cases as unsuitable.

CONCLUSIONS

The findings demonstrate that even under conditions where populations and comparators are identical and the evidence base is consistent, different assessors may arrive at divergent conclusions about comparative effectiveness, thus underscoring the presence of value judgments within assessments of clinical effectiveness. To support initiatives that seek to facilitate the exchange of value assessments between countries, these value judgments should always be transparently presented and justified in assessment summaries.

摘要

目的

我们比较了临床和经济评估研究所(ICER)对比较临床疗效的评估与德国联邦联合委员会(G-BA)的额外获益评估,并探讨了哪些因素可能解释了这两个组织之间的分歧。

方法

我们纳入了在 2020 年至 2023 年价值评估框架下由 ICER 评估、且截至 2024 年 1 月针对相同适应证、患者人群和对照药物由 G-BA 进行相应评估的药物。为了比较评估,我们修改了 ICER 提出的 G-BA 和 ICER 获益评估之间的交叉对照,以考虑 G-BA 的确定性评估。我们还确定了每一对评估是否基于相似的证据。尽管基于相似的证据基础,但经修改的交叉对照显示存在不一致的评估对,我们对其进行定性分析,以确定不一致的原因。

结果

在基于适应证、患者亚组和对照药物匹配的 15 对药物评估中,当基于相似证据时,没有一对评估结果一致。不一致归因于证据评估的差异,包括安全性、普遍性和研究设计的评估,以及 G-BA 在 4 个案例中拒绝认为现有证据不适合。

结论

研究结果表明,即使在人群和对照药物相同且证据基础一致的情况下,不同的评估者也可能对比较疗效得出不同的结论,从而强调了在临床疗效评估中存在价值判断。为了支持旨在促进国家间价值评估交流的倡议,这些价值判断应始终在评估摘要中透明地呈现和论证。

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