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Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC

Lung adenocarcinoma is the most common subtype of non-small cell lung cancer (NSCLC). With the discovery of epidermal growth factor receptor (EGFR) mutations, anaplastic lymphoma kinase (ALK) rearrangements, and effective targeted therapies, therapeutic options are expanding for patients with lung a...

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Autores principales: Bansal, Pranshu, Osman, Diaa, Gan, Gregory N., Simon, George R., Boumber, Yanis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854869/
https://www.ncbi.nlm.nih.gov/pubmed/27200298
http://dx.doi.org/10.3389/fonc.2016.00112
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author Bansal, Pranshu
Osman, Diaa
Gan, Gregory N.
Simon, George R.
Boumber, Yanis
author_facet Bansal, Pranshu
Osman, Diaa
Gan, Gregory N.
Simon, George R.
Boumber, Yanis
author_sort Bansal, Pranshu
collection PubMed
description Lung adenocarcinoma is the most common subtype of non-small cell lung cancer (NSCLC). With the discovery of epidermal growth factor receptor (EGFR) mutations, anaplastic lymphoma kinase (ALK) rearrangements, and effective targeted therapies, therapeutic options are expanding for patients with lung adenocarcinoma. Here, we review novel therapies in non-squamous NSCLC, which are directed against oncogenic targets, including EGFR, ALK, ROS1, BRAF, MET, human epidermal growth factor receptor 2 (HER2), vascular endothelial growth factor receptor 2 (VEGFR2), RET, and NTRK. With the rapidly evolving molecular testing and development of new targeted agents, our ability to further personalize therapy in non-squamous NSCLC is rapidly expanding.
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spelling pubmed-48548692016-05-19 Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC Bansal, Pranshu Osman, Diaa Gan, Gregory N. Simon, George R. Boumber, Yanis Front Oncol Oncology Lung adenocarcinoma is the most common subtype of non-small cell lung cancer (NSCLC). With the discovery of epidermal growth factor receptor (EGFR) mutations, anaplastic lymphoma kinase (ALK) rearrangements, and effective targeted therapies, therapeutic options are expanding for patients with lung adenocarcinoma. Here, we review novel therapies in non-squamous NSCLC, which are directed against oncogenic targets, including EGFR, ALK, ROS1, BRAF, MET, human epidermal growth factor receptor 2 (HER2), vascular endothelial growth factor receptor 2 (VEGFR2), RET, and NTRK. With the rapidly evolving molecular testing and development of new targeted agents, our ability to further personalize therapy in non-squamous NSCLC is rapidly expanding. Frontiers Media S.A. 2016-05-04 /pmc/articles/PMC4854869/ /pubmed/27200298 http://dx.doi.org/10.3389/fonc.2016.00112 Text en Copyright © 2016 Bansal, Osman, Gan, Simon and Boumber. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Bansal, Pranshu
Osman, Diaa
Gan, Gregory N.
Simon, George R.
Boumber, Yanis
Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC
title Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC
title_full Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC
title_fullStr Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC
title_full_unstemmed Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC
title_short Recent Advances in Targetable Therapeutics in Metastatic Non-Squamous NSCLC
title_sort recent advances in targetable therapeutics in metastatic non-squamous nsclc
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854869/
https://www.ncbi.nlm.nih.gov/pubmed/27200298
http://dx.doi.org/10.3389/fonc.2016.00112
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