Ontology highlight
ABSTRACT: Purpose
Metastatic breast cancer (mBC) patients with DPYD genetic variants linked to loss of dihydropyrimidine dehydrogenase (DPD) activity are at risk of severe capecitabine-associated toxicities. However, prospective DPYD genotyping has not yet been implemented in routine clinical practice. Following a previous internal review in which two patients underwent lengthy hospitalisations whilst receiving capecitabine, and were subsequently found to be DPD deficient, we initiated routine DPYD genotyping prior to starting capecitabine. This study evaluates the clinical application of routine DPYD screening at a large cancer centre in London.Methods
We reviewed medical records for consecutive patients with mBC who underwent DPYD genotyping before commencing capecitabine between D
SUBMITTER: Stavraka C
PROVIDER: S-EPMC6533219 | biostudies-literature | 2019 Jun
REPOSITORIES: biostudies-literature