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用于个性化癌症治疗的肿瘤分子图谱的发展态势:全面综述

Evolving landscape of tumor molecular profiling for personalized cancer therapy: a comprehensive review.

作者信息

Syn Nicholas Li-Xun, Yong Wei-Peng, Goh Boon-Cher, Lee Soo-Chin

机构信息

a Department of Haematology-Oncology , National University Cancer Institute, National University Health System , Singapore , Singapore.

出版信息

Expert Opin Drug Metab Toxicol. 2016 Aug;12(8):911-22. doi: 10.1080/17425255.2016.1196187. Epub 2016 Jun 13.

Abstract

INTRODUCTION

Tumour molecular profiling has been at the crossroads of large-scale integrative genomic studies and major clinical trials over the past 5 years and has provided roadmaps for better disease stratification and therapeutic management.

AREAS COVERED

We review the landscape of precision oncology trials in Asia, Europe and the United States, and emerging insights gained from recently reported studies such as the SHIVA and CUSTOM trials. Changes in the molecular portraits of human cancers and the immune contexture of the tumor microenvironment during treatment may predict the course of tumor progression, including the development of treatment resistance. 'Liquid biopsy' approaches that harness circulating tumor cells, cell-free DNA and exosomes may provide a non-invasive means of monitoring the parent tumor in real-time. Several molecular signatures are being evaluated as biomarkers for emerging immunologic approaches, such as the mismatch-repair deficiency status and nonsynonymous mutation burden in anti-PD-1 immune checkpoint blockade. Finally, we review the current actionability and future clinical impact of multigene panel and next-generation sequencing (NGS)-based profiling.

EXPERT OPINION

In the future, molecular profiling may help to fulfill unmet needs for predictive biomarkers in novel immunotherapeutic approaches, while ongoing precision trials are laying the foundations for clinical uptake of NGS testing.

摘要

引言

在过去5年中,肿瘤分子谱分析处于大规模综合基因组研究和重大临床试验的交叉点,并为更好的疾病分层和治疗管理提供了路线图。

涵盖领域

我们回顾了亚洲、欧洲和美国精准肿瘤学试验的概况,以及从最近报道的研究(如SHIVA和CUSTOM试验)中获得的新见解。人类癌症分子图谱的变化以及治疗期间肿瘤微环境的免疫背景可能预测肿瘤进展过程,包括耐药性的产生。利用循环肿瘤细胞、游离DNA和外泌体的“液体活检”方法可能提供一种实时监测原发肿瘤的非侵入性手段。几种分子特征正被评估为新兴免疫疗法的生物标志物,如抗PD-1免疫检查点阻断中的错配修复缺陷状态和非同义突变负担。最后,我们回顾了基于多基因检测板和下一代测序(NGS)分析的当前可操作性和未来临床影响。

专家观点

未来,分子谱分析可能有助于满足新型免疫治疗方法中预测生物标志物的未满足需求,而正在进行的精准试验正在为NGS检测的临床应用奠定基础。

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