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Clinical development of RET inhibitors in RET-rearranged non-small cell lung cancer: Update
Author(s) -
Luis Mendoza
Publication year - 2018
Publication title -
oncology reviews
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.637
H-Index - 21
eISSN - 1970-5565
pISSN - 1970-5557
DOI - 10.4081/oncol.2018.352
Subject(s) - medicine , vandetanib , lung cancer , cancer research , fluorescence in situ hybridization , oncology , proto oncogene proteins c ret , bioinformatics , tyrosine kinase , gene , receptor , biology , genetics , chromosome , neurotrophic factors , glial cell line derived neurotrophic factor
Precision oncology is now the evidence-based standard of care for the management of many advanced non-small cell lung cancers (NSCLC). Notably, new molecular profiling technologies have permitted dynamic growth in the identification of actionable driver oncogenes including rearrangements. oncogenes cannot be adequately detected by immunohistochemistry, although fluorescence hybridization, reverse transcriptase polymerase chain reaction and next-generation sequencing are complementary diagnostic tools. In the clinical setting, the benefit of the most developed RET inhibitors, ., cabozantinb, vandetanib and lenvatinb, in terms of response and median progressionfree survival has been demonstrated. The absence of striking clinical results of RET inhibitors underscores the clear need for development of more selective and potent RET inhibitors. This paper reviews the clinical data available on RET inhibitors in RET-associated NSCLC.

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