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Validation and clinical utility of prostate cancer biomarkers

机译:前列腺癌生物标志物的验证和临床应用

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To improve future drug development and patient management for patients with castration-resistant prostate cancer (CRPC), surrogate biomarkers that are linked to relevant outcomes are urgently needed. A biomarker must be measurable, reproducible, linked to relevant clinical outcomes, and demonstrate clinical utility. This area is rapidly evolving, with recent trials in patients with CRPC incorporating the detection of circulating tumour cells (CTCs), imaging, and patient-reported outcome biomarkers. We discuss the framework for the development of biomarkers for CRPC, including different categories and contexts of use. We also highlight the requirements of analytical validation, the sequence of trials needed for clinical validation and regulatory approval, and the future outlook for imaging and CTC biomarkers. ?2013 Macmillan Publishers Limited. All rights reserved.
机译:为了改善去势抵抗性前列腺癌(CRPC)患者的未来药物开发和患者管理,迫切需要与相关结果相关的替代生物标志物。生物标志物必须是可测量的,可再现的,与相关的临床结果相关联并证明其临床实用性。该领域正在迅速发展,最近在CRPC患者中进行的试验包括对循环肿瘤细胞(CTC)的检测,成像和患者报告的结局生物标记物。我们讨论了用于CRPC生物标志物开发的框架,包括不同的使用类别和使用环境。我们还将重点介绍分析验证的要求,临床验证和监管批准所需的试验顺序以及成像和CTC生物标志物的未来前景。 ?2013 Macmillan Publishers Limited。版权所有。

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