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Potential added value of combined DPYD/DPD genotyping and phenotyping to prevent severe toxicity in patients with a DPYD variant and decreased dihydropyrimidine dehydrogenase enzyme activity.

Charlotte W OckeloenAron RaaijmakersManon Hijmans-van der VegtJörgen BierauJudith de Vos-GeelenAnnelieke Ecab WillemsenBianca Jc van den BoschMarieke Jh Coenen
Published in: Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners (2021)
Our results indicate that a combined genotype-phenotype approach could be useful to identify patients at increased risk for fluoropyrimidine-associated toxicity (e.g. patients with a variant and decreased dihydropyrimidine dehydrogenase activity). Because the group sizes are too small to demonstrate statistically significant differences, this warrants further research in a prospective study in a larger cohort.
Keyphrases
  • high throughput
  • oxidative stress
  • genome wide
  • early onset
  • dna methylation
  • gene expression