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The early economic evaluation of novel biomarkers to accelerate their translation into clinical applications

机译:新型生物标志物的早期经济评价加速翻译成临床应用

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Translating prognostic and diagnostic biomarker candidates into clinical applications takes time, is very costly, and many candidates fail. It is therefore crucial to be able to select those biomarker candidates that have the highest chance of successfully being adopted in the clinic. This requires an early estimate of the potential clinical impact and commercial value. In this paper, we aim to demonstratively evaluate a set of novel biomarkers in terms of clinical impact and commercial value, using occurrence of cardiovascular disease (CVD) in type-2 diabetes (DM2) patients as a case study. We defined a clinical application for the novel biomarkers, and subsequently used data from a large cohort study in The Netherlands in a modeling exercise to assess the potential clinical impact and headroom for the biomarkers. The most likely application of the biomarkers would be to identify DM2 patients with a low CVD risk and subsequently withhold statin treatment. As a result, one additional CVD event in every 75 patients may be expected. The expected downstream savings resulted in a headroom for a point-of-care device ranging from €119.09 at a willingness to accept of €0 for one additional CVD event, to €0 at a willingness to accept of €15,614 or more. It is feasible to evaluate novel biomarkers on outcomes directly relevant to technological development and clinical adoption. Importantly, this may be attained at the same point in time and using the same data as used for the evaluation of association with disease and predictive power.
机译:将预后和诊断生物标志物候选转化为临床应用需要时间,非常昂贵,许多候选人失败。因此,能够选择那些具有最高机会成功被诊所采用的生物标志物的候选者是至关重要的。这需要早期估计潜在的临床影响和商业价值。在本文中,我们的目的是在临床影响和商业价值方面证明一组新的生物标志物,使用2型糖尿病(DM2)患者的心血管疾病(CVD)作为案例研究。我们为新型生物标志物定义了临床申请,随后在荷兰的大型队列研究中使用了建模练习中的数据,以评估生物标志物的潜在临床影响和净空。生物标志物最可能的应用是鉴定具有低CVD风险的DM2患者,随后扣留他汀类药物治疗。因此,可以预期每75名患者中的一个额外的CVD事件。预期的下游节省储蓄导致了一个额外的CVD事件的百欧元的护理点设备的净额,以便接受0欧元,以愿意接受15,614欧元以上。评估与技术开发和临床采用直接相关的成果的新型生物标志物是可行的。重要的是,这可以在同一时间点和使用与疾病和预测力的关联评估相同的数据获得。

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