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体细胞突变和免疫检查点生物标志物。

Somatic mutations and immune checkpoint biomarkers.

机构信息

University of Queensland Thoracic Research Centre, Brisbane, QLD, Australia.

Department of Thoracic Medicine, The Prince Charles Hospital, Brisbane, QLD, Australia.

出版信息

Respirology. 2019 Mar;24(3):215-226. doi: 10.1111/resp.13463. Epub 2019 Jan 12.

Abstract

The development of molecular testing for identifying somatic mutations and immune checkpoint biomarkers has directed treatment towards personalized medicine for patients with non-small cell lung cancer. The choice of molecular testing in a clinical setting is influenced by cost, expertise in the technology, instrumentation setup and sample type availability. The molecular techniques described in this review include immunohistochemistry (IHC), fluorescent in situ hybridization, direct sequencing, real-time polymerase chain reaction (PCR), denaturing high-performance liquid chromatography, matrix-assisted laser desorption/ionization time of flight mass spectrometry and next-generation sequencing (NGS). IHC is routinely used in clinical practice for the classification, differentiation, histology and identification of targetable alterations of epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK) and programmed death ligand-1 (PD-L1). Recently, the PD-L1 pathway was identified as being exploited by tumour cells, allowing immune resistance and tumour evasion. The development of immune checkpoint inhibitors as treatment for tumours expressing checkpoints has highlighted the need for standardized IHC assays to inform treatment decisions for patients. Direct sequencing was historically the gold standard for mutation testing for EGFR, KRAS (Kirsten rat sarcoma viral oncogene homologue) and BRAF (v-Raf murine sarcoma viral oncogene homologue B1) requiring a high ratio of tumour to normal cells, but this has been superseded by more sensitive methods. NGS is a new emerging technique, which allows high-throughput coverage of frequently mutated genes, including less common BRAF and MET mutations and alterations in tumour suppressor genes. When an NGS platform is unavailable, PCR-based technologies offer an efficient and cost-effective single gene test to guide patient treatment. This article will review these techniques and discuss the future of molecular platforms underpinning clinical management decisions.

摘要

针对非小细胞肺癌患者,通过识别体细胞突变和免疫检查点生物标志物的分子检测方法,推动了个性化医疗的发展。在临床环境中选择分子检测受到成本、技术专业知识、仪器设置和样本类型可用性的影响。本文中描述的分子技术包括免疫组织化学(IHC)、荧光原位杂交、直接测序、实时聚合酶链反应(PCR)、变性高效液相色谱、基质辅助激光解吸/电离飞行时间质谱和下一代测序(NGS)。IHC 已在临床实践中常规用于表皮生长因子受体(EGFR)、间变性淋巴瘤激酶(ALK)和程序性死亡配体-1(PD-L1)的分类、分化、组织学和靶向改变的鉴定。最近,PD-L1 途径被鉴定为肿瘤细胞利用的途径,允许免疫抵抗和肿瘤逃逸。免疫检查点抑制剂作为表达检查点的肿瘤的治疗方法的发展突出了标准化 IHC 检测对于为患者提供治疗决策的必要性。直接测序是 EGFR、KRAS(Kirsten 大鼠肉瘤病毒致癌基因同源物)和 BRAF(v-Raf 鼠肉瘤病毒致癌基因同源物 B1)突变检测的金标准,需要肿瘤与正常细胞的高比例,但已被更敏感的方法所取代。NGS 是一种新兴技术,它允许对经常突变的基因进行高通量覆盖,包括不太常见的 BRAF 和 MET 突变以及肿瘤抑制基因的改变。当没有 NGS 平台时,基于 PCR 的技术提供了一种高效且具有成本效益的单基因检测方法,以指导患者治疗。本文将回顾这些技术,并讨论支持临床管理决策的分子平台的未来。

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