5-Fluorouracil rechallenge after 5-fluorouracil-induced hyperammonemic encephalopathy.


Journal

Anti-cancer drugs
ISSN: 1473-5741
Titre abrégé: Anticancer Drugs
Pays: England
ID NLM: 9100823

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 12 12 2018
medline: 22 9 2020
entrez: 12 12 2018
Statut: ppublish

Résumé

For several decades, 5-Fluorouracil (5-FU) has been the backbone of many chemotherapy regimens for various tumor types. Its most common side effects are gastrointestinal disorders, mucositis, myelosuppression, hand-foot syndrome, and rarely cardiac toxicity. More rarely, 5-FU infusion can induce hyperammonemic encephalopathy. 5-FU toxicities can be worsened by complete or partial genetic and/or phenotypic dihydropyrimidine dehydrogenase deficiency. Here, we report the case of a patient who initially developed a 5-FU-induced hyperammonemic encephalopathy after receiving FOLFIRINOX (oxaliplatin, irinotecan, folinic acid, and 5-FU) chemotherapy with bevacizumab to treat a metastatic gastrointestinal cancer of unknown primary. Thereafter, the patient was rechallenged successfully by the same chemotherapy regimen (FOLFIRINOX) for more than 6 months with a protocol consisting in a free protein diet, and administration of ammonium chelators, and Krebs and urea cycle intermediates, to prevent further hyperammonemia. We also present a review of the literature on 5-FU rechallenge after 5-FU-induced hyperammonemic encephalopathy.

Identifiants

pubmed: 30531368
doi: 10.1097/CAD.0000000000000730
doi:

Substances chimiques

Oxaliplatin 04ZR38536J
Bevacizumab 2S9ZZM9Q9V
Irinotecan 7673326042
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

313-317

Auteurs

Alice Boilève (A)

Medical Oncology Department, Gustave Roussy, Université Paris-Saclay.
Paris Descartes University.

Camille Wicker (C)

Paris Descartes University.
Reference Center of Hereditary Métabolic Diseases, Imagine Institute.
Metabolic Biochemistry Department, Necker-Enfants Malades Hospital.

Benjamin Verret (B)

Medical Oncology Department, Gustave Roussy, Université Paris-Saclay.

Florence Leroy (F)

Medical Oncology Department, Gustave Roussy, Université Paris-Saclay.

David Malka (D)

Medical Oncology Department, Gustave Roussy, Université Paris-Saclay.

Mathieu Jozwiak (M)

Intensive Care Unit, Bicêtre Hospital, Paris-Sud University, APHP, Le Kremlin-Bicêtre, Paris, France.

Clément Pontoizeau (C)

Paris Descartes University.
Reference Center of Hereditary Métabolic Diseases, Imagine Institute.
Metabolic Biochemistry Department, Necker-Enfants Malades Hospital.

Chris Ottolenghi (C)

Paris Descartes University.
Reference Center of Hereditary Métabolic Diseases, Imagine Institute.
Metabolic Biochemistry Department, Necker-Enfants Malades Hospital.

Pascale De Lonlay (P)

Paris Descartes University.
Reference Center of Hereditary Métabolic Diseases, Imagine Institute.
Metabolic Biochemistry Department, Necker-Enfants Malades Hospital.

Michel Ducreux (M)

Medical Oncology Department, Gustave Roussy, Université Paris-Saclay.

Antoine Hollebecque (A)

Medical Oncology Department, Gustave Roussy, Université Paris-Saclay.

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Classifications MeSH