Gobbini Elisa, Swalduz Aurélie, Levra Matteo Giaj, Ortiz-Cuaran Sandra, Toffart Anne-Claire, Pérol Maurice, Moro-Sibilot Denis, Saintigny Pierre
Thoracic Oncology Unit, CHU Grenoble-Alpes, Grenoble 38700, France.
Univ Lyon, Université Claude Bernard Lyon, INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon 69373, France.
Cancers (Basel). 2020 Oct 24;12(11):3112. doi: 10.3390/cancers12113112.
Tumor genomic profiling has a dramatic impact on the selection of targeted treatment and for the identification of resistance mechanisms at the time of progression. Solid tissue biopsies are sometimes challenging, and liquid biopsies are used as a non-invasive alternative when tissue is limiting. The clinical relevance of tumor genotyping through analysis of ctDNA is now widely recognized at all steps of the clinical evaluation process in metastatic non-small cell lung cancer (NSCLC) patients. ctDNA analysis through liquid biopsy has recently gained increasing attention as well in the management of early and locally advanced, not oncogene-addicted, NSCLC. Its potential applications in early disease detection and the response evaluation to radical treatments are promising. The aim of this review is to summarize the landscape of liquid biopsies in clinical practice and also to provide an overview of the potential perspectives of development focusing on early detection and screening, the assessment of minimal residual disease, and its potential role in predicting response to immunotherapy. In addition to available studies demonstrating the clinical relevance of liquid biopsies, there is a need for standardization and well-designed clinical trials to demonstrate its clinical utility.
肿瘤基因组分析对靶向治疗的选择以及疾病进展时耐药机制的识别具有重大影响。实体组织活检有时具有挑战性,当组织样本有限时,液体活检可作为一种非侵入性替代方法。通过分析循环肿瘤DNA(ctDNA)进行肿瘤基因分型在转移性非小细胞肺癌(NSCLC)患者临床评估过程的各个阶段的临床相关性现已得到广泛认可。通过液体活检进行ctDNA分析最近在早期和局部晚期、非致癌基因依赖型NSCLC的管理中也越来越受到关注。其在早期疾病检测和根治性治疗反应评估中的潜在应用前景广阔。本综述的目的是总结液体活检在临床实践中的现状,并概述其在早期检测和筛查、微小残留病评估以及预测免疫治疗反应方面的潜在发展前景。除了现有研究证明液体活检的临床相关性外,还需要标准化和精心设计的临床试验来证明其临床效用。