Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4215923 | Revue des Maladies Respiratoires Actualités | 2012 | 5 Pages |
Abstract
The fusion oncogene of echinoderm microtubule-associated protein like 4 (EML4) and anaplastic lymphoma kinase (ALK) defines a new molecular subset of non-small-cell lung cancer (NSCLC). EML4-ALK was recently identified as a transforming fusion gene. Crizotinib, a small molecule tyrosine kinase inhibitor of ALK, shows significant clinical activity in the treatment of NSCLC with EML4-ALK rearrangement, and it has rapidly entered into daily clinical care. This review focuses on the biology, clinical features and diagnostic testing of EML4-ALK rearrangement. Current data on the efficacy and toxicity of crizotinib are also examined, and future directions for the treatment of NSCLC positive for ALK rearrangement are addressed.
Keywords
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Authors
D. Moro-Sibilot, A. McLeer Florin, A.-C. Toffart, S. Lantuejoul,