Kinase inhibitor-responsive genotypes in EGFR mutated lung adenocarcinomas: Moving past common point mutations or indels into uncommon kinase domain duplications and rearrangements

Translational Lung Cancer Research

Volumn 5, Issue 3, 2016, Pages 331-337

  Costa, Daniel B ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

Author keywords

C797S; Epidermal growth factor receptor (EGFR); exon 18; Exon 18 25 duplication; Exon 19; exon 20; G719X; L858R; L861Q; Rearrangement; T790M

Indexed keywords

EPIDERMAL GROWTH FACTOR RECEPTOR; PROTEIN TYROSINE KINASE INHIBITOR;

CANCER RESISTANCE; CANCER SURVIVAL; EDITORIAL; EXON; GENE DUPLICATION; GENE REARRANGEMENT; GENOTYPE; HUMAN; INDEL MUTATION; LUNG ADENOCARCINOMA; MONOTHERAPY; NEXT GENERATION SEQUENCING; POINT MUTATION; PROGRESSION FREE SURVIVAL; QUALITY OF LIFE;

EID: 84977580702     PISSN: 22186751     EISSN: 22264477     Source Type: Journal    
DOI: 10.21037/tlcr.2016.06.04     Document Type: Editorial

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