| Literature DB >> 29344953 |
Jean-Nicolas Gallant1, Christine M Lovly2.
Abstract
Although histological subtype still underlies tumour classification and treatment, the recognition that lung cancer is, largely, a genetic disease has prompted a push to reconfigure cancer taxonomies according to molecular criteria. In this review, we discuss established (e.g. EGFR, ALK, ROS1, and programmed cell death 1/programmed death-ligand 1), emerging (e.g. MET, RET, and NTRK) and elusive (e.g. TP53, KRAS, and MYC) molecular targets in the treatment of lung cancer. We synthesize a large and rapidly growing body of literature regarding the discovery and therapeutic inhibition of these targets in lung cancer.Entities:
Keywords: ALK; EGFR; PD-1; PD-L1; lung cancer; precision medicine; targeted therapy
Mesh:
Substances:
Year: 2018 PMID: 29344953 DOI: 10.1002/path.5038
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 9.883