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Rapidly progressive squamous cell lung cancer with MET exon 14 skipping mutation metastasized to atypical bone sites – a case report
Author(s) -
Kengo Nishino,
Sou Hattori,
Yukiko Kodama,
Yuika Sasatani,
Hiroaki Satoh
Publication year - 2022
Publication title -
klinicka onkologie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.204
H-Index - 13
eISSN - 1802-5307
pISSN - 0862-495X
DOI - 10.48095/ccko202272
Subject(s) - medicine , lung cancer , exon , exon skipping , pathology , oncology , biology , gene , biochemistry , alternative splicing
The mesenchymal-epithelial transition factor (MET) exon 14 skipping mutation has recently emerged as a driver gene in non-small cell lung cancer (NSCLC) in clinical practice. Clinical trials of several MET inhibitors have shown the effectiveness of MET inhibitors in NSCLC patients with MET exon 14 skipping mutation. To the best of our knowledge, however, there was no patient with sole MET exon 14 skipping mutation who progressed rapidly and had a poor prognosis.

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