5-Fluorouracil Neurotoxicity in the Absence of Dihydropyrimidine Dehydrogenase Deficiency Case Report

Rebecca Jules1, Arushi Thaper2, Ryan Foster2

  • 1University of Florida College of Medicine, Gainesville, FL, USA.

The Neurohospitalist
|April 14, 2022
PubMed

Insights

A rare 5-fluorouracil (5-FU) neurotoxicity complication occurred in a patient without DPD deficiency. Treatment with uridine triacetate led to acute, reversible neurotoxicity resolution.

Area of Science:

  • Oncology
  • Neuroscience
  • Pharmacology

Background:

  • 5-fluorouracil (5-FU) is a common chemotherapy agent.
  • Neurotoxicity is a rare but severe adverse effect of 5-FU.
  • Dihydropyrimidine dehydrogenase (DPD) deficiency increases 5-FU toxicity risk.

Observation:

  • A patient with colorectal adenocarcinoma received FOLFOX (leucovorin calcium, 5-fluorouracil, oxaliplatin).
  • The patient, without DPD deficiency, experienced acute neurotoxicity.
  • Neurotoxicity presented with global diffusion restriction on imaging.

Findings:

  • Uridine triacetate administration was followed by resolution of neurotoxicity.
  • This suggests a potential role for uridine triacetate in managing 5-FU-induced neurotoxicity.
  • The patient's lack of DPD deficiency highlights other potential mechanisms for 5-FU neurotoxicity.

Implications:

  • This case expands understanding of 5-FU neurotoxicity mechanisms.
  • Uridine triacetate may be a therapeutic option for 5-FU neurotoxicity, even in non-DPD deficient patients.
  • Further research is warranted to explore uridine triacetate's efficacy and safety in managing chemotherapy-induced neurotoxicity.