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Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer

BACKGROUND: 5-fluorouracil (5-FU) based chemotherapy is the most common first line regimen used in gastric and gastroesophageal junction cancer, but development of severe toxicity is a main concern in the treatment. The present study is aimed to evaluate a novel pre-treatment assay, known as the 5-F...

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Autores principales: Borro, Marina, Botticelli, Andrea, Mazzuca, Federica, Onesti, Elisa Concetta, Gentile, Giovanna, Romiti, Adriana, Cerbelli, Bruna, Mazzotti, Eva, Marchetti, Luca, Lionetto, Luana, Simmaco, Maurizio, Marchetti, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355161/
https://www.ncbi.nlm.nih.gov/pubmed/27738344
http://dx.doi.org/10.18632/oncotarget.12571
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author Borro, Marina
Botticelli, Andrea
Mazzuca, Federica
Onesti, Elisa Concetta
Gentile, Giovanna
Romiti, Adriana
Cerbelli, Bruna
Mazzotti, Eva
Marchetti, Luca
Lionetto, Luana
Simmaco, Maurizio
Marchetti, Paolo
author_facet Borro, Marina
Botticelli, Andrea
Mazzuca, Federica
Onesti, Elisa Concetta
Gentile, Giovanna
Romiti, Adriana
Cerbelli, Bruna
Mazzotti, Eva
Marchetti, Luca
Lionetto, Luana
Simmaco, Maurizio
Marchetti, Paolo
author_sort Borro, Marina
collection PubMed
description BACKGROUND: 5-fluorouracil (5-FU) based chemotherapy is the most common first line regimen used in gastric and gastroesophageal junction cancer, but development of severe toxicity is a main concern in the treatment. The present study is aimed to evaluate a novel pre-treatment assay, known as the 5-FU degradation rate (5-FUDR), as a predictive factor for 5-FU toxicity. METHODS: Pre-treatment 5-FUDR and gene polymorphisms related to 5-FU metabolism (DPYDIVS14+1G>A, MTHFRA1298T or C677T, TMYS TSER) were characterized in gastro-esophageal cancer patients. Association with toxicities was retrospectively evaluated, using multivariate logistic regression analysis. RESULTS: 107 gastro-esophageal cancer patients were retrospectively analyzed. No relation between gene polymorphisms and toxicity were detected, while low (< 5(th) centile) and high (> 95(th) centile) 5-FUDRs were associated with development of grade 3-4 toxicity (OR 11.14, 95% CI 1.09-113.77 and OR 9.63, 95% CI 1.70-54.55, p = 0.002). CONCLUSIONS: Compared to currently used genetic tests, the pre-treatment 5-FUDR seems useful in identifying patients at risk of developing toxicity.
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spelling pubmed-53551612017-04-15 Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer Borro, Marina Botticelli, Andrea Mazzuca, Federica Onesti, Elisa Concetta Gentile, Giovanna Romiti, Adriana Cerbelli, Bruna Mazzotti, Eva Marchetti, Luca Lionetto, Luana Simmaco, Maurizio Marchetti, Paolo Oncotarget Clinical Research Paper BACKGROUND: 5-fluorouracil (5-FU) based chemotherapy is the most common first line regimen used in gastric and gastroesophageal junction cancer, but development of severe toxicity is a main concern in the treatment. The present study is aimed to evaluate a novel pre-treatment assay, known as the 5-FU degradation rate (5-FUDR), as a predictive factor for 5-FU toxicity. METHODS: Pre-treatment 5-FUDR and gene polymorphisms related to 5-FU metabolism (DPYDIVS14+1G>A, MTHFRA1298T or C677T, TMYS TSER) were characterized in gastro-esophageal cancer patients. Association with toxicities was retrospectively evaluated, using multivariate logistic regression analysis. RESULTS: 107 gastro-esophageal cancer patients were retrospectively analyzed. No relation between gene polymorphisms and toxicity were detected, while low (< 5(th) centile) and high (> 95(th) centile) 5-FUDRs were associated with development of grade 3-4 toxicity (OR 11.14, 95% CI 1.09-113.77 and OR 9.63, 95% CI 1.70-54.55, p = 0.002). CONCLUSIONS: Compared to currently used genetic tests, the pre-treatment 5-FUDR seems useful in identifying patients at risk of developing toxicity. Impact Journals LLC 2016-10-11 /pmc/articles/PMC5355161/ /pubmed/27738344 http://dx.doi.org/10.18632/oncotarget.12571 Text en Copyright: © 2017 Borro et al. http://creativecommons.org/licenses/by/3.0/ 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 author and source are credited.
spellingShingle Clinical Research Paper
Borro, Marina
Botticelli, Andrea
Mazzuca, Federica
Onesti, Elisa Concetta
Gentile, Giovanna
Romiti, Adriana
Cerbelli, Bruna
Mazzotti, Eva
Marchetti, Luca
Lionetto, Luana
Simmaco, Maurizio
Marchetti, Paolo
Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
title Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
title_full Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
title_fullStr Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
title_full_unstemmed Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
title_short Pre-treatment assay of 5-fluorouracil degradation rate (5-FUDR) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
title_sort pre-treatment assay of 5-fluorouracil degradation rate (5-fudr) to improve prediction of 5-fluorouracil toxicity in gastro-esophageal cancer
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355161/
https://www.ncbi.nlm.nih.gov/pubmed/27738344
http://dx.doi.org/10.18632/oncotarget.12571
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