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Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers
Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2677718/ https://www.ncbi.nlm.nih.gov/pubmed/19424511 http://dx.doi.org/10.1155/2009/567486 |
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author | Harandi, Amir Zaidi, Aisha S. Stocker, Abigail M. Laber, Damian A. |
author_facet | Harandi, Amir Zaidi, Aisha S. Stocker, Abigail M. Laber, Damian A. |
author_sort | Harandi, Amir |
collection | PubMed |
description | Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of clinical trials in the management of solid malignancies have become available indicating the clinical efficacy of anti-EGFR monoclonal antibodies and oral small molecule tyrosine kinase inhibitors (TKIs). This review addresses frequently used EGFR inhibitors, summarizes clinical efficacy data of these new therapeutic agents, and discusses their associated toxicity and management. |
format | Text |
id | pubmed-2677718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-26777182009-05-07 Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers Harandi, Amir Zaidi, Aisha S. Stocker, Abigail M. Laber, Damian A. J Oncol Review Article Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of clinical trials in the management of solid malignancies have become available indicating the clinical efficacy of anti-EGFR monoclonal antibodies and oral small molecule tyrosine kinase inhibitors (TKIs). This review addresses frequently used EGFR inhibitors, summarizes clinical efficacy data of these new therapeutic agents, and discusses their associated toxicity and management. Hindawi Publishing Corporation 2009 2009-05-06 /pmc/articles/PMC2677718/ /pubmed/19424511 http://dx.doi.org/10.1155/2009/567486 Text en Copyright © 2009 Amir Harandi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Harandi, Amir Zaidi, Aisha S. Stocker, Abigail M. Laber, Damian A. Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers |
title | Clinical Efficacy and Toxicity of Anti-EGFR Therapy in
Common Cancers |
title_full | Clinical Efficacy and Toxicity of Anti-EGFR Therapy in
Common Cancers |
title_fullStr | Clinical Efficacy and Toxicity of Anti-EGFR Therapy in
Common Cancers |
title_full_unstemmed | Clinical Efficacy and Toxicity of Anti-EGFR Therapy in
Common Cancers |
title_short | Clinical Efficacy and Toxicity of Anti-EGFR Therapy in
Common Cancers |
title_sort | clinical efficacy and toxicity of anti-egfr therapy in
common cancers |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2677718/ https://www.ncbi.nlm.nih.gov/pubmed/19424511 http://dx.doi.org/10.1155/2009/567486 |
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