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Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity
5-Fluorouracil (5-FU), in combination with other cytotoxic drugs, is commonly used to treat a variety of cancers. Dihydropyrimidine dehydrogenase (DPD) catalyzes the first catabolic step of the 5-FU degradation pathway, converting 80% of 5-FU to its inactive metabolite. Approximately 0.3% of the pop...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
São Paulo, SP: Universidade de São Paulo, Hospital Universitário
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360833/ https://www.ncbi.nlm.nih.gov/pubmed/30775324 http://dx.doi.org/10.4322/acr.2018.049 |
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author | Fidai, Shiraz S. Sharma, Aarti E. Johnson, Daniel N. Segal, Jeremy P. Lastra, Ricardo R. |
author_facet | Fidai, Shiraz S. Sharma, Aarti E. Johnson, Daniel N. Segal, Jeremy P. Lastra, Ricardo R. |
author_sort | Fidai, Shiraz S. |
collection | PubMed |
description | 5-Fluorouracil (5-FU), in combination with other cytotoxic drugs, is commonly used to treat a variety of cancers. Dihydropyrimidine dehydrogenase (DPD) catalyzes the first catabolic step of the 5-FU degradation pathway, converting 80% of 5-FU to its inactive metabolite. Approximately 0.3% of the population demonstrate complete DPD deficiency, translating to extreme toxicity of 5-FU. Here we present a case of a patient who had a fatal outcome after treatment with 5-FU who was found to have an unknown DPD deficiency discovered at autopsy. |
format | Online Article Text |
id | pubmed-6360833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | São Paulo, SP: Universidade de São Paulo, Hospital Universitário |
record_format | MEDLINE/PubMed |
spelling | pubmed-63608332019-02-15 Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity Fidai, Shiraz S. Sharma, Aarti E. Johnson, Daniel N. Segal, Jeremy P. Lastra, Ricardo R. Autops Case Rep Article / Autopsy Case Report 5-Fluorouracil (5-FU), in combination with other cytotoxic drugs, is commonly used to treat a variety of cancers. Dihydropyrimidine dehydrogenase (DPD) catalyzes the first catabolic step of the 5-FU degradation pathway, converting 80% of 5-FU to its inactive metabolite. Approximately 0.3% of the population demonstrate complete DPD deficiency, translating to extreme toxicity of 5-FU. Here we present a case of a patient who had a fatal outcome after treatment with 5-FU who was found to have an unknown DPD deficiency discovered at autopsy. São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2018-11-30 /pmc/articles/PMC6360833/ /pubmed/30775324 http://dx.doi.org/10.4322/acr.2018.049 Text en Autopsy and Case Reports. ISSN 2236-1960. Copyright © 2018. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the article is properly cited. |
spellingShingle | Article / Autopsy Case Report Fidai, Shiraz S. Sharma, Aarti E. Johnson, Daniel N. Segal, Jeremy P. Lastra, Ricardo R. Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity |
title | Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity |
title_full | Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity |
title_fullStr | Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity |
title_full_unstemmed | Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity |
title_short | Dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-Fluorouracil toxicity |
title_sort | dihydropyrimidine dehydrogenase deficiency as a cause of fatal 5-fluorouracil toxicity |
topic | Article / Autopsy Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360833/ https://www.ncbi.nlm.nih.gov/pubmed/30775324 http://dx.doi.org/10.4322/acr.2018.049 |
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