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Design of clinical trials for biomarker research in oncology

机译:肿瘤生物标志物研究的临床试验设计

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摘要

The developmental pathway from discovery to clinical practice for biomarkers and biomarker-directed therapies is complex. While several issues need careful consideration, two critical issues that surround the validation of biomarkers are the choice of clinical trial design (which is based on the strength of the preliminary evidence and marker prevalence) and the biomarker assay related issues surrounding the marker assessment methods such as the reliability and reproducibility of the assay. This review focuses on trial designs for marker validation, both in the setting of early phase trials for initial validation, as well as in the context of larger definitive trials. Designs for biomarker validation are broadly classified as retrospective (i.e., using data from previously well-conducted, randomized, controlled trials) or prospective (enrichment, allcomers or adaptive). We believe that the systematic evaluation and implementation of these design strategies are essential to accelerate the clinical validation of biomarker-guided therapy, thereby taking us a step closer to the goal of personalized medicine.
机译:生物标志物和生物标志物定向疗法从发现到临床实践的发展途径是复杂的。尽管有几个问题需要仔细考虑,但围绕生物标志物验证的两个关键问题是临床试验设计的选择(基于初步证据和标志物普遍性的依据)以及围绕标志物评估方法的生物标志物测定相关问题,例如作为测定的可靠性和可重复性。这篇综述着重于标记物验证的试验设计,既包括早期阶段试验的初始验证,也包括较大的确定性试验。用于生物标志物验证的设计大致分为回顾性(即,使用以前进行良好,随机,对照试验的数据)或前瞻性(富集,所有基因或适应性)。我们认为,对这些设计策略的系统评估和实施对于加速生物标志物引导疗法的临床验证至关重要,从而使我们更接近个性化医学的目标。

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