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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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. |
format | Online Article Text |
id | pubmed-5355161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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