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The steady progress of targeted therapies, promising advances for lung cancer

Lung cancer remains one of the most complex and challenging cancers, being responsible for almost a third of all cancer deaths. This grim picture seems however to be changing, for at least a subset of lung cancers. The number of patients who can benefit from targeted therapies is steadily increasing...

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Detalles Bibliográficos
Autores principales: Bombardelli, Lorenzo, Berns, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898931/
https://www.ncbi.nlm.nih.gov/pubmed/27350784
http://dx.doi.org/10.3332/ecancer.2016.638
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author Bombardelli, Lorenzo
Berns, Anton
author_facet Bombardelli, Lorenzo
Berns, Anton
author_sort Bombardelli, Lorenzo
collection PubMed
description Lung cancer remains one of the most complex and challenging cancers, being responsible for almost a third of all cancer deaths. This grim picture seems however to be changing, for at least a subset of lung cancers. The number of patients who can benefit from targeted therapies is steadily increasing thanks to the progress made in identifying actionable driver lesions in lung tumours. The success of the latest generation of EGFR and ALK inhibitors in the clinic not only illustrates the value of targeted therapies, but also shows how almost inevitably drug resistance develops. Therefore, more sophisticated approaches are needed to achieve long-term remissions. Although there are still significant barriers to be overcome, technological advances in early detection of relevant mutations and the opportunity to test new drugs in predictive preclinical models justify the hope that we will overcome these obstacles.
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spelling pubmed-48989312016-06-27 The steady progress of targeted therapies, promising advances for lung cancer Bombardelli, Lorenzo Berns, Anton Ecancermedicalscience Review Lung cancer remains one of the most complex and challenging cancers, being responsible for almost a third of all cancer deaths. This grim picture seems however to be changing, for at least a subset of lung cancers. The number of patients who can benefit from targeted therapies is steadily increasing thanks to the progress made in identifying actionable driver lesions in lung tumours. The success of the latest generation of EGFR and ALK inhibitors in the clinic not only illustrates the value of targeted therapies, but also shows how almost inevitably drug resistance develops. Therefore, more sophisticated approaches are needed to achieve long-term remissions. Although there are still significant barriers to be overcome, technological advances in early detection of relevant mutations and the opportunity to test new drugs in predictive preclinical models justify the hope that we will overcome these obstacles. Cancer Intelligence 2016-04-28 /pmc/articles/PMC4898931/ /pubmed/27350784 http://dx.doi.org/10.3332/ecancer.2016.638 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Bombardelli, Lorenzo
Berns, Anton
The steady progress of targeted therapies, promising advances for lung cancer
title The steady progress of targeted therapies, promising advances for lung cancer
title_full The steady progress of targeted therapies, promising advances for lung cancer
title_fullStr The steady progress of targeted therapies, promising advances for lung cancer
title_full_unstemmed The steady progress of targeted therapies, promising advances for lung cancer
title_short The steady progress of targeted therapies, promising advances for lung cancer
title_sort steady progress of targeted therapies, promising advances for lung cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898931/
https://www.ncbi.nlm.nih.gov/pubmed/27350784
http://dx.doi.org/10.3332/ecancer.2016.638
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