Literature DB >> 30293943

Resistance to molecularly targeted therapy in non-small-cell lung cancer.

Tetsuhiko Asao1, Fumiyuki Takahashi2, Kazuhisa Takahashi2.   

Abstract

The discovery of oncogenic driver gene mutations, including epidermal growth factor receptor (EGFR) mutation, anaplastic lymphoma kinase (ALK) fusion, ROS proto-oncogene 1 (ROS1) fusion, and ret proto-oncogene (RET) fusion, has led to the development of molecularly targeted therapy for non-small-cell lung cancer (NSCLC). This therapy has changed the standard of care for NSCLC. Despite the dramatic response to molecularly targeted therapy, almost all patients ultimately develop resistance to the drugs. To understand the mechanisms of resistance to molecularly targeted agents, it is essential to understand the molecular pathways of NSCLC. Here, we review the mechanisms of resistance to molecularly targeted therapy and discuss strategies to overcome drug resistance.
Copyright © 2018 The Japanese Respiratory Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ALK; Acquired resistance; EGFR; Lung cancer; Molecularly targeted therapy

Mesh:

Substances:

Year:  2018        PMID: 30293943     DOI: 10.1016/j.resinv.2018.09.001

Source DB:  PubMed          Journal:  Respir Investig        ISSN: 2212-5345


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