A digital PCR assay development to detect EGFR T790M mutation in NSCLC patients

Ruifeng Zhou , Yiran Cai , Zhaoliang Li , Shuangye Shen , Mozhou Sha , Steven R. Head , Yan Wang
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引用次数: 10

Abstract

Epidermal growth factor receptor (EGFR) is a crucial factor in the development of non-small cell lung cancer (NSCLC). Tyrosine kinase inhibitor (TKI) therapy requires a sensitive and accurate assay for detection of drug resistant mutations in patients undergoing TKI-based targeted therapy. Digital polymerase chain reaction (PCR) is a highly sensitive PCR based detection method with the capability of absolute quantification. Here we present a digital PCR based liquid biopsy for EGFR T790M detection from blood samples with a low detection limit of 0.1% mutant allele frequency. The assay shows 100% concordance with test results obtained from cFDA approved ARMS PCR based EGFR mutation detection assay on FFPE tissue sections. It also demonstrated satisfactory sensitivity and specificity at 62.5% and 100% respectively. This assay can satisfy the clinical need of detecting EGFR T790M mutations at extremely low allele frequency. It can be used as both a companion diagnostic tool and a monitoring strategy for the development of drug resistance, and to evaluate therapeutic effects on disease progression.

建立了一种检测非小细胞肺癌患者EGFR T790M突变的数字PCR方法
表皮生长因子受体(EGFR)在非小细胞肺癌(NSCLC)的发展中起着至关重要的作用。酪氨酸激酶抑制剂(TKI)治疗需要一种敏感和准确的检测方法来检测接受TKI靶向治疗的患者的耐药突变。数字聚合酶链反应(PCR)是一种基于PCR的高灵敏度检测方法,具有绝对定量的能力。在这里,我们提出了一种基于数字PCR的液体活检方法,用于从血液样本中检测EGFR T790M,检测限为0.1%突变等位基因频率。该检测结果与cFDA批准的基于ARMS PCR的FFPE组织切片EGFR突变检测结果100%一致。灵敏度和特异度分别为62.5%和100%。该方法可以满足临床检测极低等位基因频率下EGFR T790M突变的需要。它既可以作为伴随诊断工具,也可以作为耐药性发展的监测策略,并可用于评估对疾病进展的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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