Literature DB >> 27122156

5-fluorouracil toxicity in the treatment of colon cancer associated with the genetic polymorphism 2846 A>G (rs67376798).

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

Mesh:

Substances:

Year:  2016        PMID: 27122156     DOI: 10.1177/1078155216647202

Source DB:  PubMed          Journal:  J Oncol Pharm Pract        ISSN: 1078-1552            Impact factor:   1.809


  3 in total

Review 1.  Colorectal Cancer Immunotherapy: Options and Strategies.

Authors:  Nor Adzimah Johdi; Nur Fazilah Sukor
Journal:  Front Immunol       Date:  2020-09-18       Impact factor: 7.561

Review 2.  Complement System: An Immunotherapy Target in Colorectal Cancer.

Authors:  Iman M Talaat; Noha Mousaad Elemam; Maha Saber-Ayad
Journal:  Front Immunol       Date:  2022-01-31       Impact factor: 7.561

Review 3.  Associating resistance to immune checkpoint inhibitors with immunological escape in colorectal cancer.

Authors:  Yi Ding; Zehua Wang; Fengmei Zhou; Chen Chen; Yanru Qin
Journal:  Front Oncol       Date:  2022-09-30       Impact factor: 5.738

  3 in total

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