A rapid, sensitive assay to detect EGFR mutation in small biopsy specimens from lung cancer

被引:169
作者
Yatabe, Yasushi [1 ]
Hida, Toyoaki
Horio, Yoshitsugu
Kosaka, Takayuki
Takahashi, Takashi
Mitsudomi, Tetsuya
机构
[1] Aichi Canc Ctr Hosp, Dept Pathol & Mol Diagnost, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Aichi Canc Ctr Hosp, Dept Thorac Oncol, Nagoya, Aichi 4648681, Japan
[3] Aichi Canc Ctr Hosp, Dept Thorac Surg, Nagoya, Aichi 4648681, Japan
[4] Nagoya Univ, Grad Sch Med, Div Mol Carcinogenesis, Ctr Neural Dis & Canc, Nagoya, Aichi, Japan
关键词
D O I
10.2353/jmoldx.2006.050104
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
It has been demonstrated that lung cancers, specifically a subset of pulmonary adenocarcinomas, with epidermal growth factor receptor (EGFR) mutation are highly sensitive to EGFR-targeted drugs. Therefore, a rapid, sensitive assay for mutation detection using routine pathological specimens is demanded in clinical practice to predict the response. We therefore developed a new assay for detecting EGFR mutation using only a paraffin section of a small biopsy specimen. The method was very sensitive, detecting as few as 5% cancer cells in a background of normal cells, the results usually being obtained within 4 hours. Furthermore, it was accurate, as shown by the high concordance with reverse transcriptase-polymerase chain reaction-coupled direct sequencing (186 of 195, 95%). The practical application of this assay to 29 cases treated with gefitinib resulted in a high prediction rate: 10 of the 11 responders were shown to be positive for the mutation, and all patients with progressive disease were negative. In addition, a mutation at codon 790, conferring gefitinib resistance, was successfully analyzed in a similar manner. in conclusion, the assay is a rapid, sensitive method using paraffin sections of biopsy specimens without a tumor cell-enrichment procedure and is quite useful to select a treatment of choice in clinical practice.
引用
收藏
页码:335 / 341
页数:7
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