Hawkins Neil, Bouttell Janet, Ponomarev Dmitry
Health Economics and Health Technology Assessment, School of Health and Wellbeing, University of Glasgow, Clarice Pears Building, 90 Byers Road, Glasgow, G12 8TB, UK.
Nottingham University Hospitals NHS Trust, QMC, Nottingham, UK.
Appl Health Econ Health Policy. 2025 Jan;23(1):65-74. doi: 10.1007/s40258-024-00906-z. Epub 2024 Sep 2.
Predictive biomarkers are intended to predict an individual's expected response to specific treatments. These are an important component of precision medicine. We explore measures of biomarker performance that are based on the expected probability of response to individual treatment conditional on biomarker status. We show how these measures can be used to establish thresholds at which testing strategies will be clinically superior.
We used a decision model to compare expected probabilities of response of treat-all and test-and-treat strategies. Based on this, R-Shiny-based apps were developed which produce plots of the threshold positive and negative predictive values or sensitivities and specificities above which a 'test-and-treat' strategy will outperform a 'treat-all' strategy. We present a case study using data on the use of RAS status to predict response to panitumumab in metastatic colorectal cancer.
Where a companion diagnostic is predictive of response to one of the treatments being compared, it is possible to estimate threshold sensitivities and specificities above which a testing strategy will outperform a treat-all strategy, based only on the odds ratio of response. Where negative and positive predictive values were used, the threshold depended on the prevalence of the biomarker-positive patients.
These intuitive performance measures for predictive biomarkers, based on expected response to individual treatments, can be used to identify promising candidate companion diagnostic tests and indicate the potential magnitude of the net benefit of testing.
预测性生物标志物旨在预测个体对特定治疗的预期反应。这些是精准医学的重要组成部分。我们探讨基于生物标志物状态下个体治疗反应预期概率的生物标志物性能测量方法。我们展示了如何使用这些测量方法来确定测试策略在临床上更具优势的阈值。
我们使用决策模型比较全面治疗和检测后治疗策略的预期反应概率。基于此,开发了基于R-Shiny的应用程序,该程序生成阈值阳性和阴性预测值或敏感性和特异性的图表,高于这些值时,“检测后治疗”策略将优于“全面治疗”策略。我们使用关于RAS状态用于预测转移性结直肠癌中帕尼单抗反应的数据进行了案例研究。
当伴随诊断能够预测对所比较的一种治疗的反应时,仅基于反应的优势比,就有可能估计出阈值敏感性和特异性,高于这些值时,检测策略将优于全面治疗策略。当使用阴性和阳性预测值时,阈值取决于生物标志物阳性患者的患病率。
这些基于对个体治疗预期反应的预测性生物标志物直观性能测量方法,可用于识别有前景的候选伴随诊断测试,并表明检测净效益的潜在大小。