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KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies

Survival of patients with metastatic CRC (mCRC) has improved steadily over the past several decades, due largely to the development of new combinations of standard chemotherapy, as well as to the introduction of new targeted therapies. Among the available targeted therapies are two monoclonal antibo...

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Autores principales: Soulières, D., Greer, W., Magliocco, Anthony M., Huntsman, D., Young, S., Tsao, M.-S., Kamel-Reid, S.
Formato: Texto
Lenguaje:English
Publicado: Multimed Inc. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901795/
https://www.ncbi.nlm.nih.gov/pubmed/20680106
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author Soulières, D.
Greer, W.
Magliocco, Anthony M.
Huntsman, D.
Young, S.
Tsao, M.-S.
Kamel-Reid, S.
author_facet Soulières, D.
Greer, W.
Magliocco, Anthony M.
Huntsman, D.
Young, S.
Tsao, M.-S.
Kamel-Reid, S.
author_sort Soulières, D.
collection PubMed
description Survival of patients with metastatic CRC (mCRC) has improved steadily over the past several decades, due largely to the development of new combinations of standard chemotherapy, as well as to the introduction of new targeted therapies. Among the available targeted therapies are two monoclonal antibodies that target the epidermal growth factor receptor (EGFR) – cetuximab and panitumumab – which have demonstrated efficacy in the treatment of mCRC. These therapies are associated with a unique set of toxicities and costs, prompting the need for tools to select patients who are most likely to derive a benefit from them. Mutations in the KRAS oncogene have consistently been shown to predict non-response to cetuximab and panitumumab. The role of KRAS as a marker of efficacy of anti-EGFR therapies is reviewed.
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spelling pubmed-29017952010-08-02 KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies Soulières, D. Greer, W. Magliocco, Anthony M. Huntsman, D. Young, S. Tsao, M.-S. Kamel-Reid, S. Curr Oncol Medical Oncology Survival of patients with metastatic CRC (mCRC) has improved steadily over the past several decades, due largely to the development of new combinations of standard chemotherapy, as well as to the introduction of new targeted therapies. Among the available targeted therapies are two monoclonal antibodies that target the epidermal growth factor receptor (EGFR) – cetuximab and panitumumab – which have demonstrated efficacy in the treatment of mCRC. These therapies are associated with a unique set of toxicities and costs, prompting the need for tools to select patients who are most likely to derive a benefit from them. Mutations in the KRAS oncogene have consistently been shown to predict non-response to cetuximab and panitumumab. The role of KRAS as a marker of efficacy of anti-EGFR therapies is reviewed. Multimed Inc. 2010-07 /pmc/articles/PMC2901795/ /pubmed/20680106 Text en 2010 Multimed Inc. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Medical Oncology
Soulières, D.
Greer, W.
Magliocco, Anthony M.
Huntsman, D.
Young, S.
Tsao, M.-S.
Kamel-Reid, S.
KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies
title KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies
title_full KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies
title_fullStr KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies
title_full_unstemmed KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies
title_short KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies
title_sort kras mutation testing in the treatment of metastatic colorectal cancer with anti-egfr therapies
topic Medical Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2901795/
https://www.ncbi.nlm.nih.gov/pubmed/20680106
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