Results 81 to 90 of about 4,744 (194)

New advances in DPYD genotype and risk of severe toxicity under capecitabine. [PDF]

open access: yesPLoS ONE, 2017
Deficiency in dihydropyrimidine dehydrogenase (DPD) enzyme is the main cause of severe and lethal fluoropyrimidine-related toxicity. Various approaches have been developed for DPD-deficiency screening, including DPYD genotyping and phenotyping.
Marie-Christine Etienne-Grimaldi   +32 more
doaj   +1 more source

Frequency and clinical impact of DPYD gene variants

open access: yes
Abstract Introduction and objective: The aim of this study was to determine the prevalence of loss-of-function variants in the DPYD gene in patients with solid tumours who have undergone genotyping and establish the clinical results of this implementation in clinical practice in four hospitals in the Balearic Islands. Methods: The study was descriptive,
GÓMEZ ZAMORA, M   +7 more
openaire   +2 more sources

DPYD Genotyping, Fluoropyrimidine Dosage and Toxicity: An Umbrella Review of Systematic Reviews

open access: yesPharmaceuticals
Background/Objectives: Fluoropyrimidines are widely used chemotherapeutic agents in various solid tumors. Germline variants in the DPYD gene, which encodes the enzyme dihydropyrimidine dehydrogenase (DPD), are known to impair drug metabolism and increase
Sara Otero-Torres   +6 more
doaj   +1 more source

Study of polymorphisms of UGT1A1 and DPYD genes in chemotherapy for colorectal cancer

open access: yesСибирский онкологический журнал, 2019
Background. The personalized approach implies an individual choice of medicines and their doses for the patient, providing the most effective and safe pharmacotherapy. Objective: analysis of the frequencies of UGT1A1 and DPYD polymorphisms and comparison
N. N. Timoshkina   +7 more
doaj   +1 more source

Feasibility of DPYD Genotyping in Australian Cancer Patients

open access: yes, 2023
Abstract Background. Fluoropyrimidine (FP) chemotherapies are widely prescribed for solid organ malignancies, including colorectal, gastrointestinal, breast and head and neck cancers. They are prescribed for over 10,000 Australian cancer patients per year.
Cassandra White   +7 more
openaire   +1 more source

Development and analytical validation of a targeted short‐read next generation sequencing‐based pharmacogenetic panel for comprehensive variant detection

open access: yesBritish Journal of Pharmacology, Volume 183, Issue 16, Page 4735-4760, August 2026.
Abstract Background and Purpose Genomic profiling of patients for genetic variants that modify the effect of specific medications has many benefits, including the possibility of avoiding toxicities and ensuring an adequate effect of the medication. Our intention was to develop a comprehensive, high‐quality pharmacogenetic test panel for clinical use ...
Anna Gréen   +5 more
wiley   +1 more source

Pharmacogenetic Practice of Anticancer Drugs: Multiple Approaches for an Accurate and Comprehensive Genotyping

open access: yesPharmacogenomics and Personalized Medicine, 2023
Cristina Montrasio,1 Stefania Cheli,1 Emilio Clementi2,3 1Unit of Clinical Pharmacology, ASST Fatebenefratelli Sacco, L. Sacco University Hospital, Milan, Italy; 2Clinical Pharmacology Unit, Department of Biomedical and Clinical Sciences, L.
Montrasio C, Cheli S, Clementi E
doaj  

Near Miss or Standard of Care? DPYD Screening for Cancer Patients Receiving Fluorouracil

open access: yesCurrent Oncology, 2020
5-fluorouracil (5-FU) and its pro-drug capecitabine are widely used anticancer agents. Most 5-FU catabolism is dependent on dihydropyrimidine dehydrogenase (DPD) encoded by the DPYD gene, and DPYD variants that reduce DPD function increase 5-FU toxicity.
Lauren E. Winquist   +3 more
doaj   +1 more source

Mutational spectrum of dihydropyrimidine dehydrogenase gene (DPYD) in the Tunisian population.

open access: yes, 2007
Dihydropyrimidine dehydrogenase enzyme (DPD) deficiency is a pharmacogenetic syndrome leading to severe side-effects in patients receiving therapies containing the anticancer drug 5-fluorouracil (5-FU).
Ben Fredj, R;Gross, E;Chouchen, L;B'Chir, F;Ben Ahmed, S;Neubauer, S;Kiechle, M;Saguem, S
core   +1 more source

A Serverless Pharmacogenomic Risk Dashboard: Translating Ensemble Models and Model‐Based Scenario Rules to Clinical Decision Support

open access: yesClinical and Translational Science, Volume 19, Issue 8, August 2026.
ABSTRACT The “last mile” problem in healthcare AI—translating high‐performance models into accessible, privacy‐preserving point‐of‐care tools—remains unsolved for pharmacogenomic (PGx) risk assessment. No existing platform integrates opioid and polypharmacy risk scoring, model‐based scenario analysis, and CPIC‐based PGx patient cards within a single ...
R. Jerome Dixon, Elvin T. Price
wiley   +1 more source

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