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对非鳞状非小细胞肺癌中潜在可操作靶点进行扩展分子检测。

Expanded molecular interrogation for potential actionable targets in non-squamous non-small cell lung cancer.

作者信息

Lau Kah Weng, Seng Claudia, Lim Tony K H, Tan Daniel S W

机构信息

Department of Anatomical Pathology, Singapore General Hospital, Singapore.

Institute of Molecular and Cell Biology, ASTAR, Singapore.

出版信息

Ann Transl Med. 2017 Sep;5(18):372. doi: 10.21037/atm.2017.08.42.

Abstract

The advent of targeted therapies has established new standards of care for defined molecular subsets of non-small cell lung cancer (NSCLC). Not only has this led to significant changes in the routine clinical management of lung cancer e.g., multiplexed genomic testing, but it has provided important principles and benchmarks for determining "actionability". At present, the clinical paradigms are most evolved for EGFR mutations and ALK rearrangements, where multiple randomized phase III trials have determined optimal treatment strategies in both treatment naïve and resistant settings. However, this may not always be feasible with low prevalence alterations e.g., ROS1 and BRAF mutations. Another emerging observation is that not all targets are equally "actionable", necessitating a rigorous preclinical, clinical and translational framework to prosecute new targets and drug candidates. In this review, we will cover the role of targeted therapies for NSCLC harbouring BRAF, MET, HER2 and RET alterations, all of which have shown promise in non-squamous non-small cell lung cancer (ns-NSCLC). We further review some early epigenetic targets in NSCLC, an area of emerging interest. With increased molecular segmentation of lung cancer, we discuss the upcoming challenges in drug development and implementation of precision oncology approaches, especially in light of the complex and rapidly evolving therapeutic landscape.

摘要

靶向治疗的出现为非小细胞肺癌(NSCLC)特定分子亚群确立了新的治疗标准。这不仅给肺癌的常规临床管理带来了重大变革,例如多重基因组检测,还为确定“可操作性”提供了重要原则和基准。目前,针对表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)重排的临床模式发展最为成熟,多项随机III期试验已确定了初治和耐药情况下的最佳治疗策略。然而,对于低发生率的改变,如ROS1和BRAF突变,这种方法可能并不总是可行。另一个新出现的观察结果是,并非所有靶点都同样具有“可操作性”,因此需要一个严格的临床前、临床和转化框架来推进新靶点和候选药物的研究。在这篇综述中,我们将探讨靶向治疗对携带BRAF、MET、HER2和RET改变的NSCLC的作用,所有这些改变在非鳞状非小细胞肺癌(ns-NSCLC)中都显示出了前景。我们还将进一步综述NSCLC中一些新出现的早期表观遗传靶点。随着肺癌分子分型的增加,我们将讨论药物开发以及精准肿瘤学方法实施过程中即将面临挑战,特别是鉴于复杂且快速演变的治疗格局。

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