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国家生物标志物开发联盟:应对生物标志物研发生产力低下的问题。

The national biomarker development alliance: confronting the poor productivity of biomarker research and development.

作者信息

Poste George, Compton Carolyn C, Barker Anna D

机构信息

NBDA, Arizona State University, SkySong, 1475 N. Scottsdale Rd., Suite 361, Scottsdale, AZ 85257, USA.

出版信息

Expert Rev Mol Diagn. 2015 Feb;15(2):211-8. doi: 10.1586/14737159.2015.974561. Epub 2014 Nov 25.

Abstract

Making precision (personalized) medicine a routine clinical reality will require a comprehensive inventory of validated biomarkers and molecular diagnostic tests to stratify disease subtypes and improve accuracy in diagnosis and treatment selection. Realization of this promise has been hindered by the poor productivity of biomarker identification and validation. This situation reflects deficiencies that are pervasive across the entire spectrum of biomarker R&D, from discovery to clinical validation and in the failure of regulatory and reimbursement policies to accommodate new classes of biomarkers. The launch of the National Biomarker Development Alliance is the culmination of a 2-year review and consultation process involving diverse stakeholders to advance standards, best practices and guidelines to enhance biomarker discovery and validation by adoption of systems-based approaches and trans-sector collaboration between academia, clinical medicine and relevant private and public sector stakeholders.

摘要

要使精准(个性化)医疗成为常规临床现实,将需要对经过验证的生物标志物和分子诊断测试进行全面梳理,以对疾病亚型进行分层,并提高诊断和治疗选择的准确性。生物标志物识别和验证的低效率阻碍了这一愿景的实现。这种情况反映出在生物标志物研发的整个过程中普遍存在的缺陷,从发现到临床验证,以及监管和报销政策未能适应新类型生物标志物。国家生物标志物开发联盟的成立是一个为期两年的审查和咨询过程的成果,该过程涉及不同的利益相关者,旨在通过采用基于系统的方法以及学术界、临床医学与相关私营和公共部门利益相关者之间的跨部门合作,推进标准、最佳实践和指南,以加强生物标志物的发现和验证。

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