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用于患者选择和分层的基因组生物标志物:癌症范例。

Genomic biomarkers for patient selection and stratification: the cancer paradigm.

作者信息

Moschos Sterghios Athanasios

机构信息

Molecular & Applied Biosciences, School of Life Sciences, University of Westminster, London, W1W 6UW, UK.

出版信息

Bioanalysis. 2012 Oct;4(20):2499-511. doi: 10.4155/bio.12.241.

Abstract

The revolution in disease diagnosis and treatment promised on the completion of the human genome project over a decade ago has materialized in the form of unified drug and biomarker discovery and development pipelines. This strategic shift has been principally catalyzed through success stories in the field of oncology, ushering in the era of personalized medicine. Thus, a number of molecular targets have also been demonstrated to be reliable markers for selecting patients wherein treatment can be efficacious. Perhaps more importantly, however, the late adoption of biomarker strategies has also rescued drug candidates from complete late-stage failure. This review examines the historical lessons of key challenges in translating biomarker assay information into strategic and clinically actionable decisions and assesses the impact of personalized genome sequencing in the future of companion diagnostic development and commercialization.

摘要

十多年前人类基因组计划完成时所承诺的疾病诊断和治疗革命,已以统一的药物和生物标志物发现与开发流程的形式得以实现。这一战略转变主要是由肿瘤学领域的成功案例所催化,从而迎来了个性化医疗时代。因此,一些分子靶点也已被证明是选择治疗有效的患者的可靠标志物。然而,或许更重要的是,生物标志物策略的后期采用也使候选药物免于完全的后期失败。本综述探讨了将生物标志物检测信息转化为战略和临床可行决策过程中关键挑战的历史教训,并评估了个性化基因组测序在伴随诊断开发和商业化未来中的影响。

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