Targeted therapy for lung cancer: Beyond EGFR and ALK

Author:

Herrera‐Juárez Mercedes12ORCID,Serrano‐Gómez Cristina1,Bote‐de‐Cabo Helena12,Paz‐Ares Luis123

Affiliation:

1. Department of Medical Oncology Hospital Universitario 12 de Octubre Madrid Spain

2. H12O‐CNIO Lung Cancer Clinical Research Unit Health Research Institute Hospital Universitario 12 de Octubre Madrid Spain

3. Department of Medicine Complutense University Madrid Spain

Abstract

AbstractPrecision oncology comprises the set of strategies that aim to design the best cancer treatment based on tumor biology. A recognized subset of patients with non‐small 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.

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference120 articles.

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