Steady-state pharmacokinetics and metabolism of voriconazole in patients

被引:58
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
相关论文
共 34 条
[1]   Antifungal Therapeutic Drug Monitoring: Established and Emerging Indications [J].
Andes, David ;
Pascual, Andres ;
Marchetti, Oscar .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (01) :24-34
[2]  
[Anonymous], 2012, FACH VFEND
[3]   Pharmacokinetics and safety of 14 days intravenous voriconazole in allogeneic haematopoietic stem cell transplant recipients [J].
Bruggemann, Roger J. M. ;
Blijlevens, N. M. A. ;
Burger, David M. ;
Franke, Barbara ;
Troke, Peter F. ;
Donnelly, J. Peter .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2010, 65 (01) :107-113
[4]   Pharmacokinetics of oral voriconazole in patients with cystic fibrosis [J].
Clifton, Ian J. ;
Whitaker, Paul ;
Metcalfe, Rachel ;
Phillip, Maria ;
Shaw, Nicola ;
Conway, Steven P. ;
Peckham, Daniel G. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2011, 66 (10) :2438-2440
[5]   Multicenter Study of Voriconazole Pharmacokinetics and Therapeutic Drug Monitoring [J].
Dolton, Michael J. ;
Ray, John E. ;
Chen, Sharon C. -A. ;
Ng, Kingsley ;
Pont, Lisa G. ;
McLachlan, Andrew J. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (09) :4793-4799
[6]   Voriconazole - a new therapeutic agent with an extended spectrum of antifungal activity [J].
Donnelly, JP ;
De Pauw, BE .
CLINICAL MICROBIOLOGY AND INFECTION, 2004, 10 :107-117
[7]   Safety and pharmacokinetics of coadministered voriconazole and anidulafungin [J].
Dowell, JA ;
Schranz, J ;
Baruch, A ;
Foster, G .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (12) :1373-1382
[8]   Induction of voriconazole metabolism by rifampin in a patient with acute myeloid leukemia: Importance of interdisciplinary communication to prevent treatment errors with complex medications [J].
Geist, Marcus J. P. ;
Egerer, Gerlinde ;
Burhenne, Juergen ;
Riedel, Klaus-Dieter ;
Mikus, Gerd .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (09) :3455-3456
[9]   Safety of voriconazole in a patient with CYP2C9*2/CYP2C9*2 genotype [J].
Geist, Marcus J. P. ;
Egerer, Gerlinde ;
Burhenne, Juergen ;
Mikus, Gerd .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (09) :3227-3228
[10]   Clinical relevance of genetic polymorphisms in the human CYP2C subfamily [J].
Goldstein, JA .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 52 (04) :349-355