Jing Chang-Wen, Wang Zhuo, Cao Hai-Xia, Ma Rong, Wu Jian-Zhong
Clinical Cancer Research Center, Jiangsu Cancer Hospical, Nanjing, China E-mail :
Asian Pac J Cancer Prev. 2014 Jan;14(11):6619-23. doi: 10.7314/apjcp.2013.14.11.6619.
The aim of the research was to explore a cost effective, fast, easy to perform, and sensitive method for epidermal growth factor receptor (EGFR) mutation testing.
High resolution melting analysis (HRM) was introduced to evaluate the efficacy of the analysis for dectecting EGFR mutations in exons 18 to 21 using formalin-fixed paraffin-embedded (FFPE) tissues and plasma free DNA from 120 patients.
The total EGFR mutation rate was 37.5% (45/120) detected by direct sequencing. There were 48 mutations in 120 FFPE tissues assessed by HRM. For plasma free DNA, the EGFR mutation rate was 25.8% (31/120). The sensitivity of HRM assays in FFPE samples was 100% by HRM. There was a low false-positive mutation rate but a high false-negative rate in plasma free DNA detected by HRM.
Our results show that HRM analysis has the advantage of small tumor sample need. HRM applied with plasma free DNA showed a high false-negative rate but a low false-positive rate. Further research into appropriate methods and analysis needs to be performed before HRM for plasma free DNA could be accepted as an option in diagnostic or screening settings.
本研究的目的是探索一种经济高效、快速、易于操作且灵敏的表皮生长因子受体(EGFR)突变检测方法。
引入高分辨率熔解分析(HRM),以评估使用福尔马林固定石蜡包埋(FFPE)组织和120例患者的游离血浆DNA检测外显子18至21中EGFR突变的分析效能。
直接测序检测到的总EGFR突变率为37.5%(45/120)。通过HRM评估的120个FFPE组织中有48个突变。对于游离血浆DNA,EGFR突变率为25.8%(31/120)。HRM检测FFPE样本的敏感性为100%。HRM检测的游离血浆DNA假阳性突变率低,但假阴性率高。
我们的结果表明,HRM分析具有所需肿瘤样本量小的优势。HRM应用于游离血浆DNA显示假阴性率高但假阳性率低。在HRM用于游离血浆DNA可被接受作为诊断或筛查手段之前,需要对合适的方法和分析进行进一步研究。