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Journal article

Clinical implementation of pre-treatment DPYD genotyping in capecitabine-treated metastatic breast cancer patients

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 December 2014 and December 2017. Patients were tested for four DPYD variants associated with reduced DPD activity. Results Sixty-six patients underwent DPYD testing. Five (8.4%) patients were found to carry DPYD genetic polymorphisms associated with reduced DPD activity; of these, two received dose-reduced capecitabine. Of the 61 patients with DPYD wild-type, 14 (23%) experienced grade 3 toxicities which involved palmar–plantar erythrodysesthesia (65%), and gastrointestinal toxicities (35%); no patient was hospitalised due to toxicity. Conclusions Prospective DPYD genotyping can be successfully implemented in routine clinical practice and can reduce the risk of severe fluoropyrimidine toxicities
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/s10549-019-05144-9

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Role:
Author
ORCID:
0000-0001-7623-299X
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Role:
Author
ORCID:
0000-0001-9469-6069
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Role:
Author
ORCID:
0000-0002-3831-0165
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-0752-1960


Publisher:
Springer
Journal:
Breast Cancer Research and Treatment More from this journal
Volume:
175
Issue:
2
Pages:
511-517
Publication date:
2019-02-11
DOI:
EISSN:
1573-7217
ISSN:
0167-6806


Language:
English
Keywords:
Pubs id:
2370893
Local pid:
pubs:2370893
Source identifiers:
W2913296433
Deposit date:
2026-02-13
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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