Srivastava Sudhir, Gray Joe W, Reid Brian J, Grad Oren, Greenwood Addison, Hawk Ernest T
Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland, USA.
Clin Cancer Res. 2008 Sep 15;14(18):5672-7. doi: 10.1158/1078-0432.CCR-08-1267.
The Translational Research Working Group (TRWG) was created as a national initiative to evaluate the current status of National Cancer Institute's investment in translational research and envision its future. The TRWG conceptualized translational research as a set of six developmental processes or pathways focused on various clinical goals. One of those pathways describes the development of biospecimen-based assays that use biomarkers for the detection, diagnosis, and prognosis of cancer and the assessment of response to cancer treatment. The biospecimen-based assessment modality pathway was conceived not as comprehensive description of the corresponding real-world processes but rather as a tool designed to facilitate movement of a candidate assay through the translational process to the point where it can be handed off for definitive clinical testing. This paper introduces the pathway in the context of prior work and discusses key challenges associated with the biomarker development process in light of the pathway.
转化研究工作组(TRWG)是作为一项全国性倡议而设立的,旨在评估美国国立癌症研究所(National Cancer Institute)在转化研究方面的投资现状并展望其未来。TRWG将转化研究概念化为一组围绕各种临床目标的六个发展过程或途径。其中一条途径描述了基于生物样本的检测方法的开发,这些方法使用生物标志物进行癌症的检测、诊断和预后评估以及对癌症治疗反应的评估。基于生物样本的评估方式途径并非旨在全面描述相应的实际过程,而是作为一种工具,旨在促进候选检测方法在转化过程中推进,直至可以交付进行确定性临床试验。本文在先前工作的背景下介绍了该途径,并根据该途径讨论了与生物标志物开发过程相关的关键挑战。