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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.
Abstract:
5 fluorouracil (5-FU)-related neurotoxicity is a rare and severe complication of 5-FU administration. Dihydropyrimidine dehydrogenase (DPD) deficiency is associated with an increased risk of serious adverse reactions due to its role in 5-FU metabolism. We report a case of acute reversible neurotoxicity with global areas of diffusion restriction in a patient with colorectal adenocarcinoma being treated with leucovorin calcium, 5-fluorouracil, and oxaliplatin (FOLFOX) without DPD deficiency following uridine triacetate administration.
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.
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