| Literature DB >> 27122156 |
Itamar González-Perera1, Fernando Gutiérrez-Nicolás2, Gloria J Nazco-Casariego1, Ruth Ramos-Díaz3, Raquel Hernández-San Gil1, José A Pérez-Pérez4, Jonathan González García1, Guillermo A González De La Fuente1.
Abstract
Colorectal cancer is the second most common cancer in Europe. Most antineoplastic regimens in first-line treatment involve 5-fluorouracil or oral prodrug capecitabine, combined with other antineoplastic agents such as oxaliplatin or irinotecan. It is well known that 5-fluorouracil and capecitabine are agents that can be toxic in cases of decreased dihydropyrimidine dehydrogenase activity because this enzyme is the main limiting factor in the metabolism of both agents. In this paper, we describe the case of a patient who developed severe toxicity to 5-fluouracil and who had a mutation in the gene encoding the enzyme dihydropyrimidine dehydrogenase.Entities:
Keywords: 2846 A>G; DPYD; fluorouracil; rs67376798; toxicity
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Year: 2016 PMID: 27122156 DOI: 10.1177/1078155216647202
Source DB: PubMed Journal: J Oncol Pharm Pract ISSN: 1078-1552 Impact factor: 1.809