Precision oncology comprises the set of strategies that aim to design the best cancer treatment based on tumor biology. A recognized subset of patients with nonsmall cell lung cancer (NSCLC) harbor actionable genomic aberrations that can benefit from targeted therapy. In lung cancer, epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) rearrangements are well characterized oncogenic drivers for which the therapeutic use of tyrosine kinase inhibitors has demonstrated improved outcomes compared with chemotherapy.Other druggable targets are also well characterized, and effective inhibitors have been developed and commercialized, leading to a paradigm shift in NSCLC treatment. Here, the authors provide a review of the oncogenic role of the most relevant molecular alterations in NSCLC and emerging treatments in this setting beyond EGFR-driven and ALK-driven diseases.
K E Y W O R D Sdriver mutations, genomic aberrations, nonsmall cell lung cancer (NSCLC), targeted therapy, tyrosine kinase inhibitors (TKI) 18.9 months with osimertinib versus 10.2 months with firstgeneration EGFR inhibitors (hazard ratio [HR], 0.46; 95% confidence interval [CI], 0.37-0.57) 6 in patients with EGFR-mutant NSCLC and 37.8 months with alectinib versus 23.0 months with crizotinib, respectively (HR, 0.43; 95% CI, 0.32-0.58), 7 in those with ALK-driven NSCLC. This has guided a consecutive generation of TKIs to regulatory approval and has established them as the standard of care for patients with EGFR-mutant and ALK-rearranged tumors in the first-line context for advanced NSCLC.