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Important Role of the Dihydrouracil/Uracil Ratio in Marked Interpatient Variations of Fluoropyrimidine Pharmacokinetics and Pharmacodynamics
Author(s) -
Jiang Hao,
Lu Jing,
Jiang Ji,
Hu Pei
Publication year - 2004
Publication title -
the journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.92
H-Index - 116
eISSN - 1552-4604
pISSN - 0091-2700
DOI - 10.1177/0091270004268911
Subject(s) - pharmacokinetics , pharmacodynamics , floxuridine , dihydropyrimidine dehydrogenase , pharmacology , fluorouracil , antimetabolite , medicine , prodrug , uracil , chemistry , methotrexate , gastroenterology , chemotherapy , thymidylate synthase , biochemistry , dna
Dihydropyrimidine dehydrogenase (DPD) deficiency in patients causes severe toxicities in 5‐fluorouracil/floxuridine (5‐FU/FUDR) treatments. To determine the plasma dihydrouracil/uracil ratio (DUUR) as a potential index for setting 5‐FU/FUDR doses, the authors conducted a prospective study on the relationships of the DUUR with 5‐FU/FUDR pharmacokinetic and pharmacodynamic parameters. Forty gestational trophoblastic tumor (GTT) patients were treated with 30 mg/kg of 5‐FU or prodrug FUDR during a 10‐day cycle. The pretreatment DUURs of the patients were determined prior to the treatments, and plasma 5‐FU and FUDR concentrations on day 1 of the test cycle were measured to calculate the corresponding pharmacokinetic parameters. The absolute neutrophil count (ANC) and human chorionic gonadotrophins (HCG/β‐HCG) were recorded as the efficacy indexes. The correlation of the DUUR with pharmacokinetic parameters and efficacy indexes was analyzed to look for a relationship between individual doses (in milligrams) and the varied DUUR. Pretreatment DUUR was significantly correlated with the corresponding plasma AUC ( r > 0.80, P < .01), the plasma drug clearance ( r > 0.78, P < .01), the ANC ( r > 0.76, P < 0.01), and the decrease of HCG/β‐HCG levels ( r > 0.5, P < 0.01). In addition, the charts for setting 5‐FU/FUDR doses were designed for further validation in clinical trials. These findings indicate the important roles of the DUUR in remarkable interpatient variations of fluoropyrimidine pharmacokinetics and pharmacodynamics and propose a better index for setting individual 5‐FU/FUDR doses based on interpatient variations in DPD levels.