Steady-state pharmacokinetics and metabolism of voriconazole in patients

被引:57
作者
Geist, Marcus J. P. [1 ]
Egerer, Gerlinde [2 ]
Burhenne, Juergen [1 ]
Riedel, Klaus-Dieter [1 ]
Weiss, Johanna [1 ]
Mikus, Gerd [1 ]
机构
[1] Univ Heidelberg Hosp, Dept Clin Pharmacol & Pharmacoepidemiol, D-69120 Heidelberg, Germany
[2] Univ Heidelberg Hosp, Dept Internal Med Haematol Oncol & Rheumatol 5, D-69120 Heidelberg, Germany
关键词
exposure variability; therapeutic drug monitoring; voriconazole-N-oxide; hydroxy-voriconazole; dihydroxy; voriconazole; TRIAZOLE ANTIFUNGAL AGENT; POPULATION PHARMACOKINETICS; INTRAVENOUS VORICONAZOLE; TRANSPLANT RECIPIENTS; ORAL VORICONAZOLE; CYP2C19; GENOTYPE; DOSE-ESCALATION; SAFETY; EFFICACY; SPECTRUM;
D O I
10.1093/jac/dkt229
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Voriconazole exhibits non-linear pharmacokinetics in adults and is said to be mainly metabolized by CYP2C19 and CYP3A4 to voriconazole-N-oxide. The aim of this study was to obtain data on steady-state pharmacokinetics after dosing for at least 14 days in patients taking additional medication and in vivo data on metabolites other than voriconazole-N-oxide. Patients and methods: Thirty-one patients receiving voriconazole as regular therapeutic drug treatment during hospitalization participated in this prospective study. Pharmacokinetic profiles were obtained for the 12 h (dosing interval) after the first orally administered dose (400 mg) or (if possible and) after an orally administered maintenance dose (200 mg) following intake for at least 14 days (n = 14 after first dose; n = 23 after maintenance dose). Blood and urine samples were collected and the concentrations of voriconazole and three of its metabolites (the N-oxide, hydroxy-voriconazole and dihydroxy-voriconazole) were determined, as well as the CYP2C19 genotype of the patients. All other drugs taken by the participating patients were evaluated. Results: A high variability of exposure (AUC) after the first dose was slightly reduced during steady-state dosing for voriconazole (82% to 71%) and the N-oxide (86% to 56%), remained high for hydroxy-voriconazole (79%) and even increased for dihydroxy-voriconazole (97% to 127%). In 16 of the 22 steady-state patients, trough plasma concentrations were <2 mu g/mL. N-oxide plasma concentrations during steady state stayed almost constant. Hydroxylations of voriconazole seem to be quantitatively more important in its metabolism than N-oxidation. Conclusions: High variability in voriconazole exposure, as well as low steady-state trough plasma concentrations, suggest that the suggested steady-state dosage of 200 mg twice a day has to be increased to prevent disease progression. Therapeutic drug monitoring is probably necessary to optimize the voriconazole dose for individual patients.
引用
收藏
页码:2592 / 2599
页数:8
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