T790米
数字聚合酶链反应
液体活检
突变
医学
活检
肺癌
表皮生长因子受体
病理
胎儿游离DNA
癌症研究
分子生物学
癌症
肿瘤科
基因
内科学
聚合酶链反应
生物
遗传学
吉非替尼
胎儿
产前诊断
怀孕
作者
Catarina Silveira,Ana Carla Sousa,André Janeiro,Sara Malveiro,Encarnação Teixeira,Eva Brysch,Marcos Pantarotto,M. Felizardo,Rosa Madureira,Fernando Neves Nogueira,Cátia Guimarães,Cristina Matos,Dolores Canário,Jácome Bruges‐Armas,Maria Carmo‐Fonseca
标识
DOI:10.21037/tlcr-20-1010
摘要
Liquid biopsy allows the identification of targetable cancer mutations in a minimally invasive manner. In patients with advanced non-small cell lung cancer (NSCLC), droplet digital PCR (ddPCR) is increasingly used to genotype the epidermal growth factor receptor (EGFR) gene in circulating cell-free DNA (cfDNA). However, the sensitivity of this method is still under debate. The aim of this study was to implement and assess the performance of a ddPCR assay for detecting the EGFR T790M mutation in liquid biopsies.A ddPCR assay was optimized to detect the EGFR T790M mutation in plasma samples from 77 patients with NSCLC in progression.Our ddPCR assay enabled the detection and quantification of the EGFR T790M mutation at cfDNA allele frequency as low as 0.5%. The mutation was detected in 40 plasma samples, corresponding to a positivity rate of 52%. The number of mutant molecules per mL of plasma ranged from 1 to 6,000. A re-biopsy was analyzed for 12 patients that had a negative plasma test and the mutation was detected in 2 cases. A second liquid biopsy was performed for 6 patients and the mutation was detected in 3 cases.This study highlights the value of ddPCR to detect and quantify the EGFR T790M mutation in liquid biopsies in a real-world clinical setting. Our results suggest that repeated ddPCR tests in cfDNA may obviate tissue re-biopsy in patients unable to provide a tumor tissue sample suitable for molecular analysis.
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