An evaluation study of EGFR mutation tests utilized for non-small-cell lung cancer in the diagnostic setting

作者:Goto K*; Satouchi M; Ishii G; Nishio K; Hagiwara K; Mitsudomi T; Whiteley J; Donald E; McCormack R; Todo T
来源:Annals of Oncology, 2012, 23(11): 2914-2919.
DOI:10.1093/annonc/mds121

摘要

Epidermal growth factor receptor (EGFR) mutation is predictive for the efficacy of EGFR tyrosine kinase inhibitors in advanced non-small-cell lung cancer (NSCLC) treatment. We evaluated the performance, sensitivity, and concordance between five EGFR tests. %26lt;br%26gt;DNA admixtures (n = 34; 1%-50% mutant plasmid DNA) and samples from NSCLC patients [116 formalin-fixed paraffin-embedded (FFPE) tissue, 29 matched bronchofiberscopic brushing (BB) cytology, and 20 additional pleural effusion (PE) cytology samples] were analyzed. EGFR mutation tests were PCR-Invader (R), peptide nucleic acid-locked nucleic acid PCR clamp, direct sequencing, Cycleave (TM), and Scorpion Amplification Refractory Mutation System (ARMS)(R). Analysis success, mutation status, and concordance rates were assessed. %26lt;br%26gt;All tests except direct sequencing detected four mutation types at %26gt;= 1% mutant DNA. Analysis success rates were 91.4%-100% (FFPE) and 100% (BB and PE cytology), respectively. Inter-assay concordance rates of successfully analyzed samples were 94.3%-100% (FFPE; kappa coefficients: 0.88-1.00), 93.1%-100% (BB cytology; 0.86-1.00), and 85.0%-100% (PE cytology; 0.70-1.00), and 93.1%-96.6% (0.86-0.93) between BB cytology and matched FFPE. %26lt;br%26gt;All EGFR assays carried out comparably in the analysis of FFPE and cytology samples. Cytology-derived DNA is a viable alternative to FFPE samples for analyzing EGFR mutations.

  • 出版日期2012-11