Drug interaction between voriconazole and tacrolimus and its association with the bioavailability of oral voriconazole in recipients of allogeneic hematopoietic stem cell transplantation

被引:46
作者
Mori, Takehiko [1 ]
Kato, Jun [1 ]
Yamane, Akiko [1 ]
Sakurai, Masatoshi [1 ]
Kohashi, Sumiko [1 ]
Kikuchi, Taku [1 ]
Ono, Yukako [1 ]
Okamoto, Shinichiro [1 ]
机构
[1] Keio Univ, Sch Med, Dept Med, Div Hematol,Shinjuku Ku, Tokyo 1608582, Japan
关键词
Voriconazole; Tacrolimus; Drug interaction; Hematopoietic stem cell transplantation; CALCINEURIN INHIBITORS; PHARMACOKINETICS; CYCLOSPORINE; CYP3A5; SAFETY; POLYMORPHISMS; INFECTIONS; THERAPY;
D O I
10.1007/s12185-012-1057-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a previous study, we noted wide inter-individual variability in drug interactions between voriconazole and tacrolimus, but that analysis did not take into account the routes of administration. In the present study, we analyzed interactions between these two drugs when both agents were administered orally after allogeneic hematopoietic stem cell transplantation (HSCT); the effect of plasma voriconazole levels on the magnitude of the drug interaction was also examined. Twenty-five allogeneic HSCT recipients were evaluated. Trough concentrations of tacrolimus were measured prior to, and periodically for 7-10 days after, initiating voriconazole (400 mg/day) to determine the concentration/dose (C/D) ratio of tacrolimus. The median C/D ratio of tacrolimus increased significantly from 172.8 (range 28.6-1110.7) to 537.5 (range 127.8-1933.3) (ng/mL)/(mg/kg) ( < 0.01) following initiation of voriconazole; the median increase was 138.8 % (range -32.0 to 685.7 %). The plasma concentration of voriconazole did not correlate with the increase of the tacrolimus C/D ratio (rho = 0.16, = 0.44). These results indicate that oral voriconazole has a significant drug interaction with oral tacrolimus with a wide inter-individual variability, which cannot be explained by the bioavailability of voriconazole. Other possible mechanisms should be explored in future studies.
引用
收藏
页码:564 / 569
页数:6
相关论文
共 28 条
[1]   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
[2]   Pharmacokinetic-pharmacodynamic consequences and clinical relevance of cytochrome P450 3A4 inhibition [J].
Dresser, GK ;
Spence, JD ;
Bailey, DG .
CLINICAL PHARMACOKINETICS, 2000, 38 (01) :41-57
[3]  
DYKEWICZ CA, 2006, BIOL BLOOD MARROW TR, V6, P670
[4]   The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients [J].
Haufroid, V ;
Mourad, M ;
Van Kerckhove, V ;
Wawrzyniak, J ;
De Meyer, M ;
Eddour, DC ;
Malaise, J ;
Lison, D ;
Squifflet, JP ;
Wallemacq, P .
PHARMACOGENETICS, 2004, 14 (03) :147-154
[5]   Voriconazole versus amphotericin B for primary therapy of invasive aspergillosis [J].
Herbrecht, R ;
Denning, DW ;
Patterson, TF ;
Bennett, JE ;
Greene, RE ;
Oestmann, JW ;
Kern, WV ;
Marr, KA ;
Ribaud, P ;
Lortholary, O ;
Sylvester, R ;
Rubin, RH ;
Wingard, JR ;
Stark, P ;
Durand, C ;
Caillot, D ;
Thiel, E ;
Chandrasekar, PH ;
Hodges, MR ;
Schlamm, HT ;
Troke, PF ;
de Pauw, B .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (06) :408-415
[6]   Treatment of invasive Candida and invasive Aspergillus infections in adult haematological patients [J].
Herbrecht, Raoul ;
Flueckiger, Ursula ;
Gachot, Bertrand ;
Ribaud, Patricia ;
Thiebaut, Anne ;
Cordonnier, Catherine .
EJC SUPPLEMENTS, 2007, 5 (02) :49-59
[7]   Genetic polymorphisms of the CYP3A4, CYP3A5, and MDR-1 genes and pharmacokinetics of the calcineurin inhibitors cyclosporine and tacrolimus [J].
Hesselink, DA ;
van Schaik, RHN ;
van der Heiden, IP ;
van der Werf, M ;
Gregoor, PJHS ;
Lindemans, J ;
Weimar, W ;
van Gelder, T .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2003, 74 (03) :245-254
[8]   Transporters and drug therapy: Implications for drug disposition and disease [J].
Ho, RH ;
Kim, RB .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 78 (03) :260-277
[9]  
Inc Pfizer, 2010, VFEND VOR PACK INS
[10]   Voriconazole [J].
Jeu, L ;
Piacenti, FJ ;
Lyakhovetskiy, AG ;
Fung, HB .
CLINICAL THERAPEUTICS, 2003, 25 (05) :1321-1381