| Literature DB >> 28444624 |
Biagio Ricciuti1, Marta Brambilla2, Giulio Metro2, Sara Baglivo2, Roberta Matocci2, Matteo Pirro3, Rita Chiari2.
Abstract
In the era of personalized medicine, the identification of targetable genetic alterations represented a major step forward in anticancer therapy. NTRK rearrangements represent the molecular driver of a subset of solid tumors, including 3% of non-small-cell lung cancers (NSCLCs). Preliminary data indicate that molecularly selected NSCLC patients harboring NTRK fusions derive an unprecedented clinical benefit from Trk-directed targeted therapies. The aim of this review is to describe the molecular biology of NTRK signaling pathway and to summarize the preclinical data on novel Trk inhibitors, touching upon the clinical development of these inhibitors for the treatment of advanced NSCLC, which have already shown encouraging anticancer activity and acceptable safety profile in early phase I clinical trials.Entities:
Keywords: Entrectinib; LOXO-101; NSCLC; NTRK mutations
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Year: 2017 PMID: 28444624 DOI: 10.1007/s12032-017-0967-5
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064