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Impact of KRAS Mutations on Management of Colorectal Carcinoma
The epidermal growth factor receptor (EGFR) pathway is a therapeutic target in the management of colorectal cancer (CRC). EGFR antagonists are active in this disease; however, only a subset of patients respond to such therapy. A Kirsten ras sarcoma viral oncogene (KRAS) wild-type (WT) status of the...
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Formato: | Texto |
Lenguaje: | English |
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SAGE-Hindawi Access to Research
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062096/ https://www.ncbi.nlm.nih.gov/pubmed/21437184 http://dx.doi.org/10.4061/2011/219309 |
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author | Sullivan, Kevin M. Kozuch, Peter S. |
author_facet | Sullivan, Kevin M. Kozuch, Peter S. |
author_sort | Sullivan, Kevin M. |
collection | PubMed |
description | The epidermal growth factor receptor (EGFR) pathway is a therapeutic target in the management of colorectal cancer (CRC). EGFR antagonists are active in this disease; however, only a subset of patients respond to such therapy. A Kirsten ras sarcoma viral oncogene (KRAS) wild-type (WT) status of the tumor is necessary, but possibly not sufficient, for a response to anti-EGFR monoclonal antibody therapy. Mechanisms of primary resistance to such therapy in patients harboring KRAS WT tumors are discussed. Strategies to overcome resistance to anti-EGFR monoclonal antibody therapy, including novel agents and combinations of novel therapies, are explored. Also, the use of anti-EGFR monoclonal antibodies in the adjuvant and neoadjuvant setting is reviewed. |
format | Text |
id | pubmed-3062096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SAGE-Hindawi Access to Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-30620962011-03-24 Impact of KRAS Mutations on Management of Colorectal Carcinoma Sullivan, Kevin M. Kozuch, Peter S. Patholog Res Int Review Article The epidermal growth factor receptor (EGFR) pathway is a therapeutic target in the management of colorectal cancer (CRC). EGFR antagonists are active in this disease; however, only a subset of patients respond to such therapy. A Kirsten ras sarcoma viral oncogene (KRAS) wild-type (WT) status of the tumor is necessary, but possibly not sufficient, for a response to anti-EGFR monoclonal antibody therapy. Mechanisms of primary resistance to such therapy in patients harboring KRAS WT tumors are discussed. Strategies to overcome resistance to anti-EGFR monoclonal antibody therapy, including novel agents and combinations of novel therapies, are explored. Also, the use of anti-EGFR monoclonal antibodies in the adjuvant and neoadjuvant setting is reviewed. SAGE-Hindawi Access to Research 2011-03-15 /pmc/articles/PMC3062096/ /pubmed/21437184 http://dx.doi.org/10.4061/2011/219309 Text en Copyright © 2011 K. M. Sullivan and P. S. Kozuch. 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 Sullivan, Kevin M. Kozuch, Peter S. Impact of KRAS Mutations on Management of Colorectal Carcinoma |
title | Impact of KRAS Mutations on Management of Colorectal Carcinoma |
title_full | Impact of KRAS Mutations on Management of Colorectal Carcinoma |
title_fullStr | Impact of KRAS Mutations on Management of Colorectal Carcinoma |
title_full_unstemmed | Impact of KRAS Mutations on Management of Colorectal Carcinoma |
title_short | Impact of KRAS Mutations on Management of Colorectal Carcinoma |
title_sort | impact of kras mutations on management of colorectal carcinoma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3062096/ https://www.ncbi.nlm.nih.gov/pubmed/21437184 http://dx.doi.org/10.4061/2011/219309 |
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