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Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment

Fluorouracil (5FU) is the backbone chemotherapy agent in the treatment of colorectal cancer (CRC). Cardiotoxicity represents an uncommon but serious side effect of treatment with 5FU. Here, we review the current literature on 5FU-cardiotoxicity in the setting of CRC specifically, with a focus on dat...

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Autores principales: Anaka, Matthew, Abdel-Rahman, Omar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799936/
https://www.ncbi.nlm.nih.gov/pubmed/35115827
http://dx.doi.org/10.2147/CMAR.S273544
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author Anaka, Matthew
Abdel-Rahman, Omar
author_facet Anaka, Matthew
Abdel-Rahman, Omar
author_sort Anaka, Matthew
collection PubMed
description Fluorouracil (5FU) is the backbone chemotherapy agent in the treatment of colorectal cancer (CRC). Cardiotoxicity represents an uncommon but serious side effect of treatment with 5FU. Here, we review the current literature on 5FU-cardiotoxicity in the setting of CRC specifically, with a focus on data from the modern era of combination chemotherapy. Despite decades of study, there is little consensus on risk factors and biomarkers for 5FU-cardiotoxicity, nor how patients with CRC should be managed following a cardiotoxicity event. Given the elevated risk of recurrent cardiotoxicity on rechallenge, the use of alternative regimens that do not contain 5FU is a critical aspect of management. Data on the cardiotoxicity risk and efficacy of non-5FU regimens in CRC are therefore reviewed in detail.
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spelling pubmed-87999362022-02-02 Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment Anaka, Matthew Abdel-Rahman, Omar Cancer Manag Res Review Fluorouracil (5FU) is the backbone chemotherapy agent in the treatment of colorectal cancer (CRC). Cardiotoxicity represents an uncommon but serious side effect of treatment with 5FU. Here, we review the current literature on 5FU-cardiotoxicity in the setting of CRC specifically, with a focus on data from the modern era of combination chemotherapy. Despite decades of study, there is little consensus on risk factors and biomarkers for 5FU-cardiotoxicity, nor how patients with CRC should be managed following a cardiotoxicity event. Given the elevated risk of recurrent cardiotoxicity on rechallenge, the use of alternative regimens that do not contain 5FU is a critical aspect of management. Data on the cardiotoxicity risk and efficacy of non-5FU regimens in CRC are therefore reviewed in detail. Dove 2022-01-23 /pmc/articles/PMC8799936/ /pubmed/35115827 http://dx.doi.org/10.2147/CMAR.S273544 Text en © 2022 Anaka and Abdel-Rahman. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Anaka, Matthew
Abdel-Rahman, Omar
Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment
title Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment
title_full Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment
title_fullStr Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment
title_full_unstemmed Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment
title_short Managing 5FU Cardiotoxicity in Colorectal Cancer Treatment
title_sort managing 5fu cardiotoxicity in colorectal cancer treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799936/
https://www.ncbi.nlm.nih.gov/pubmed/35115827
http://dx.doi.org/10.2147/CMAR.S273544
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