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肿瘤学中预测、预后和系列生物标志物检测的成本效益分析建议

Towards Recommendations for Cost-Effectiveness Analysis of Predictive, Prognostic, and Serial Biomarker Tests in Oncology.

作者信息

Kramer Astrid, van Schaik Lucas F, van den Broek Daan, Meijer Gerrit A, Gutierrez Ibarluzea Iñaki, Galnares Cordero Lorea, Fijneman Remond J A, Ligtenberg Marjolijn J L, Schuuring Ed, van Harten Wim H, Coupé Veerle M H, Retèl Valesca P

机构信息

Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Pharmacoeconomics. 2025 May;43(5):483-497. doi: 10.1007/s40273-025-01470-7. Epub 2025 Feb 8.

Abstract

BACKGROUND

Cost-effectiveness analysis (CEA) of biomarkers is challenging due to the indirect impact on health outcomes and the lack of sufficient fit-for-purpose data. Hands-on guidance is lacking.

OBJECTIVE

We aimed firstly to explore how CEAs in the context of three different types of biomarker applications have addressed these challenges, and secondly to develop recommendations for future CEAs.

METHODS

A scoping review was performed for three biomarker applications: predictive, prognostic, and serial testing, in advanced non-small cell lung cancer, early-stage colorectal cancer, and all-stage colorectal cancer, respectively. Information was extracted on the model assumptions and uncertainty, and the reported outcomes. An in-depth analysis of the literature was performed describing the impact of model assumptions in the included studies.

RESULTS

A total of 43 CEAs were included (31 predictive, 6 prognostic, and 6 serial testing). Of these, 40 utilized different sources for test and treatment parameters, and three studies utilized a single source. Test performance was included in 78% of these studies utilizing different sources, but this parameter was differently expressed across biomarker applications. Sensitivity analyses for test performance was only performed in half of these studies. For the linkage of test results to treatments outcomes, a minority of the studies explored the impact of suboptimal adherence to test results, and/or explored potential differences in treatment effects for different biomarker subgroups. Intermediate outcomes were reported by 67% of studies.

CONCLUSIONS

We identified various approaches for dealing with challenges in CEAs of biomarker tests for three different biomarker applications. Recommendations on assumptions, handling uncertainty, and reported outcomes were drafted to enhance modeling practices for future biomarker cost-effectiveness evaluations.

摘要

背景

由于生物标志物对健康结果的间接影响以及缺乏足够的适用数据,对其进行成本效益分析(CEA)具有挑战性。目前缺乏实际操作指南。

目的

我们的目标一是探讨在三种不同类型的生物标志物应用背景下,CEA是如何应对这些挑战的;二是为未来的CEA制定建议。

方法

分别对晚期非小细胞肺癌、早期结直肠癌和全阶段结直肠癌中的三种生物标志物应用(预测性、预后性和系列检测)进行了一项范围综述。提取了有关模型假设和不确定性以及报告结果的信息。对文献进行了深入分析,描述了模型假设在纳入研究中的影响。

结果

共纳入43项CEA(31项预测性、6项预后性和6项系列检测)。其中,40项研究使用了不同来源的检测和治疗参数,3项研究使用了单一来源。在这些使用不同来源的研究中,78%纳入了检测性能,但该参数在不同生物标志物应用中的表达方式不同。只有一半的研究对检测性能进行了敏感性分析。对于检测结果与治疗结果的关联,少数研究探讨了对检测结果依从性欠佳的影响,和/或探讨了不同生物标志物亚组在治疗效果上的潜在差异。67%的研究报告了中间结果。

结论

我们确定了针对三种不同生物标志物应用在生物标志物检测的CEA中应对挑战的各种方法。起草了关于假设、处理不确定性和报告结果的建议,以加强未来生物标志物成本效益评估的建模实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab44/12011951/b20a9854ad85/40273_2025_1470_Fig1_HTML.jpg

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