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Molecular profiling in the treatment of colorectal cancer: focus on regorafenib

Metastatic colorectal cancer (mCRC) is a highly heterogeneous disease. Its treatment outcome has been significantly improved over the last decade with the incorporation of biological targeted therapies, including anti-EGFR antibodies, cetuximab and panitumumab, and VEGF inhibitors, bevacizumab, ramu...

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Detalles Bibliográficos
Autores principales: Yan, Yiyi, Grothey, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610887/
https://www.ncbi.nlm.nih.gov/pubmed/26508880
http://dx.doi.org/10.2147/OTT.S79145
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author Yan, Yiyi
Grothey, Axel
author_facet Yan, Yiyi
Grothey, Axel
author_sort Yan, Yiyi
collection PubMed
description Metastatic colorectal cancer (mCRC) is a highly heterogeneous disease. Its treatment outcome has been significantly improved over the last decade with the incorporation of biological targeted therapies, including anti-EGFR antibodies, cetuximab and panitumumab, and VEGF inhibitors, bevacizumab, ramucirumab, and aflibercept. The identification of predictive biomarkers has further improved the survival by accurately selecting patients who are most likely to benefit from these treatments, such as RAS mutation profiling for EGFR antibodies. Regorafenib is a multikinase inhibitor currently used as late line therapy for mCRC. The molecular and genetic markers associated with regorafenib treatment response are yet to be characterized. Here, we review currently available clinical evidence of mCRC molecular profiling, such as RAS, BRAF, and MMR testing, and its role in targeted therapies with special focus on regorafenib treatment.
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spelling pubmed-46108872015-10-27 Molecular profiling in the treatment of colorectal cancer: focus on regorafenib Yan, Yiyi Grothey, Axel Onco Targets Ther Review Metastatic colorectal cancer (mCRC) is a highly heterogeneous disease. Its treatment outcome has been significantly improved over the last decade with the incorporation of biological targeted therapies, including anti-EGFR antibodies, cetuximab and panitumumab, and VEGF inhibitors, bevacizumab, ramucirumab, and aflibercept. The identification of predictive biomarkers has further improved the survival by accurately selecting patients who are most likely to benefit from these treatments, such as RAS mutation profiling for EGFR antibodies. Regorafenib is a multikinase inhibitor currently used as late line therapy for mCRC. The molecular and genetic markers associated with regorafenib treatment response are yet to be characterized. Here, we review currently available clinical evidence of mCRC molecular profiling, such as RAS, BRAF, and MMR testing, and its role in targeted therapies with special focus on regorafenib treatment. Dove Medical Press 2015-10-15 /pmc/articles/PMC4610887/ /pubmed/26508880 http://dx.doi.org/10.2147/OTT.S79145 Text en © 2015 Yan and Grothey. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Yan, Yiyi
Grothey, Axel
Molecular profiling in the treatment of colorectal cancer: focus on regorafenib
title Molecular profiling in the treatment of colorectal cancer: focus on regorafenib
title_full Molecular profiling in the treatment of colorectal cancer: focus on regorafenib
title_fullStr Molecular profiling in the treatment of colorectal cancer: focus on regorafenib
title_full_unstemmed Molecular profiling in the treatment of colorectal cancer: focus on regorafenib
title_short Molecular profiling in the treatment of colorectal cancer: focus on regorafenib
title_sort molecular profiling in the treatment of colorectal cancer: focus on regorafenib
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610887/
https://www.ncbi.nlm.nih.gov/pubmed/26508880
http://dx.doi.org/10.2147/OTT.S79145
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