免疫检查点抑制剂在法国卫生当局进行的卫生技术评估中的总体生存外推评估综述。

A Review of Overall Survival Extrapolations of Immune-Checkpoint Inhibitors Used in Health Technology Assessments by the French Health Authorities.

机构信息

Market access department, Bristol Myers Squibb France, Rueil-Malmaison, France.

Vyoo Agency, Lyon, France.

出版信息

Int J Technol Assess Health Care. 2022 Mar 25;38(1):e28. doi: 10.1017/S0266462322000125.

Abstract

OBJECTIVES

Extrapolation is often required to inform cost-effectiveness (CE) evaluations of immune-checkpoint inhibitors (ICIs) since survival data from pivotal clinical trials are seldom complete. The objectives of this study were to evaluate the accuracy of estimates of long-term overall survival (OS) predicted in French CE assessment reports of ICIs, and to identify models presenting the best fit to the observed long-term survival data.

METHODS

A systematic review of French assessment reports of ICIs in the metastatic setting since inception until May 2020 was performed. A targeted literature review was conducted to collect associated extended follow-up of randomized controlled trials (RCTs) used in the CE assessment reports. Difference between projected and observed OS was calculated. A range of standard parametric and spline-based models were applied to the extended follow-up data from the RCT to determine the best-fitting survival models.

RESULTS

Of the 121 CE assessment reports published, 11 reports met the inclusion criteria. OS was underestimated in 73 percent of the CE assessment reports. The mean relative difference between each source was -13 percent (median: -15 percent; IQR: -0.4 to 26 percent). Models providing the best fit were those that could reflect nonmonotonic hazards.

CONCLUSIONS

Based on the available data at the time of submission, longer-term survival of ICIs was not fully captured by the extrapolation models used in CE assessments. Standard and flexible parametric models which can capture nonmonotonic hazard functions provided the best fit to the extended follow-up data. However, these models may still have performed poorly if fitted to survival data available at the time of submission to the French National Authority for Health.

摘要

目的

由于关键性临床试验的生存数据很少完整,因此通常需要外推来为免疫检查点抑制剂(ICI)的成本效益(CE)评估提供信息。本研究的目的是评估法国 CE 评估报告中预测的长期总生存(OS)估计的准确性,并确定与观察到的长期生存数据拟合最好的模型。

方法

对截至 2020 年 5 月,法国转移性环境下 ICI 的 CE 评估报告进行了系统回顾。进行了有针对性的文献回顾,以收集相关的 RCT 扩展随访,这些 RCT 用于 CE 评估报告。计算预测的 OS 与观察到的 OS 之间的差异。对 RCT 的扩展随访数据应用了一系列标准参数和样条模型,以确定最佳拟合的生存模型。

结果

在已发表的 121 份 CE 评估报告中,有 11 份报告符合纳入标准。在 73%的 CE 评估报告中,OS 被低估。每个来源之间的平均相对差异为-13%(中位数:-15%;IQR:-0.4 至 26%)。能够反映非单调风险的模型提供了最佳拟合。

结论

根据提交时可用的数据,CE 评估中使用的外推模型并未充分捕捉到 ICI 的长期生存情况。可以捕捉非单调危险函数的标准和灵活参数模型对扩展随访数据提供了最佳拟合。然而,如果这些模型拟合的是提交给法国国家卫生管理局时可用的生存数据,则它们的表现可能仍然不佳。

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