Optimizing fluoropyrimidine therapy: Real‐world impact of <i>DPYD</i> genotype‐based dosing on severe toxicity rates

DPYD genotype-based dosing resulted in comparable incidences of severe fluoropyrimidine-related toxicity between wild-type patients and DPYD variant allele carriers. The updated guideline recommendation on dosing of C.1236G>A and C.2846A>T variant carriers appears adequate from a toxicity perspective. Our findings highlight the need to perform an individual dose titration, especially in C.1236G>A variant carriers.

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Publication Details

Journal
British Journal of Clinical Pharmacology
Published
2025-08-30
DOI
https://doi.org/10.1002/bcp.70266
Citations
1
Primary Topic
Colorectal Cancer Treatments and Studies
Type
article
Field-Weighted Citation Impact
1.05
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article

Optimizing fluoropyrimidine therapy: Real‐world impact of DPYD genotype‐based dosing on severe toxicity rates

Karin H. Herbschleb, Ankie M. Harmsze, A. Kan, Marcel P. H. van den Broek
1 citations
British Journal of Clinical Pharmacology
Colorectal Cancer Treatments and Studies
1.05
article

Optimizing fluoropyrimidine therapy: Real‐world impact of DPYD genotype‐based dosing on severe toxicity rates

Karin H. Herbschleb, Ankie M. Harmsze, A. Kan, Marcel P. H. van den Broek
article en
1 citations

Abstract

DPYD genotype-based dosing resulted in comparable incidences of severe fluoropyrimidine-related toxicity between wild-type patients and DPYD variant allele carriers. The updated guideline recommendation on dosing of C.1236G>A and C.2846A>T variant carriers appears adequate from a toxicity perspective. Our findings highlight the need to perform an individual dose titration, especially in C.1236G>A variant carriers.

British Journal of Clinical PharmacologyVol. 92(1)
University of Applied Sciences Utrecht (NL), Utrecht University (NL), St. Antonius Ziekenhuis (NL)
Openalex Percentile: Top 18%
Colorectal Cancer Treatments and Studies
1.05
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