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Recent advances of novel targeted therapy in non-small cell lung cancer
Lung cancer is the leading cause of cancer deaths world-wide. Recent advances in cancer biology have led to the identification of new targets in neoplastic cells and the development of novel targeted therapies. At this time, two targeted agents are approved by the FDA in advanced non-small cell lung...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637898/ https://www.ncbi.nlm.nih.gov/pubmed/19159467 http://dx.doi.org/10.1186/1756-8722-2-2 |
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author | Katzel, Jed A Fanucchi, Michael P Li, Zujun |
author_facet | Katzel, Jed A Fanucchi, Michael P Li, Zujun |
author_sort | Katzel, Jed A |
collection | PubMed |
description | Lung cancer is the leading cause of cancer deaths world-wide. Recent advances in cancer biology have led to the identification of new targets in neoplastic cells and the development of novel targeted therapies. At this time, two targeted agents are approved by the FDA in advanced non-small cell lung cancer (NSCLC): the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) erlotinib, and the anitangiogenic bevacizumab. A third agent, cetuximab, which was recently shown to enhance survival when used with cisplatin and vinorelbine as first line therapy for advanced NSCLC, will likely be approved by regulatory agencies. With more than 500 molecularly targeted agents under development, the prospects of identifying novel therapies that benefit individual patients with lung cancer are bright. |
format | Text |
id | pubmed-2637898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26378982009-02-10 Recent advances of novel targeted therapy in non-small cell lung cancer Katzel, Jed A Fanucchi, Michael P Li, Zujun J Hematol Oncol Review Lung cancer is the leading cause of cancer deaths world-wide. Recent advances in cancer biology have led to the identification of new targets in neoplastic cells and the development of novel targeted therapies. At this time, two targeted agents are approved by the FDA in advanced non-small cell lung cancer (NSCLC): the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) erlotinib, and the anitangiogenic bevacizumab. A third agent, cetuximab, which was recently shown to enhance survival when used with cisplatin and vinorelbine as first line therapy for advanced NSCLC, will likely be approved by regulatory agencies. With more than 500 molecularly targeted agents under development, the prospects of identifying novel therapies that benefit individual patients with lung cancer are bright. BioMed Central 2009-01-21 /pmc/articles/PMC2637898/ /pubmed/19159467 http://dx.doi.org/10.1186/1756-8722-2-2 Text en Copyright © 2009 Katzel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Katzel, Jed A Fanucchi, Michael P Li, Zujun Recent advances of novel targeted therapy in non-small cell lung cancer |
title | Recent advances of novel targeted therapy in non-small cell lung cancer |
title_full | Recent advances of novel targeted therapy in non-small cell lung cancer |
title_fullStr | Recent advances of novel targeted therapy in non-small cell lung cancer |
title_full_unstemmed | Recent advances of novel targeted therapy in non-small cell lung cancer |
title_short | Recent advances of novel targeted therapy in non-small cell lung cancer |
title_sort | recent advances of novel targeted therapy in non-small cell lung cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2637898/ https://www.ncbi.nlm.nih.gov/pubmed/19159467 http://dx.doi.org/10.1186/1756-8722-2-2 |
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