Effect of itraconazole on the concentrations of tacrolimus and cyclosporine in the blood of patients receiving allogeneic hematopoietic stem cell transplants

被引:39
作者
Nara, Miho [1 ]
Takahashi, Naoto [1 ]
Miura, Masatomo [2 ]
Niioka, Takenori [2 ]
Kagaya, Hideaki [2 ]
Fujishima, Naohito [3 ]
Saitoh, Hirobumi [1 ]
Kameoka, Yoshihiro [1 ]
Tagawa, Hiroyuki [1 ]
Hirokawa, Makoto [4 ]
Sawada, Kenichi [1 ]
机构
[1] Akita Univ, Grad Sch Med, Dept Hematol Nephrol & Rheumatol, Akita 0108543, Japan
[2] Akita Univ Hosp, Dept Pharm, Akita, Japan
[3] Akita Univ Hosp, Div Blood Transfus, Akita, Japan
[4] Akita Univ Hosp, Clin Oncol Ctr, Akita, Japan
关键词
Itraconazole; Tacrolimus; Cyclosporine; Blood concentration; Allogeneic hematopoietic stem cell transplantation; CALCINEURIN INHIBITORS; ORAL ITRACONAZOLE; DRUG-INTERACTIONS; HUMAN LIVER; CYP3A5; PHARMACOKINETICS; FLUCONAZOLE; PHARMACOGENETICS; PHARMACODYNAMICS; POLYMORPHISMS;
D O I
10.1007/s00228-013-1471-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to investigate the interactions of itraconazole (ITCZ) with orally administered calcineurin inhibitors (CNIs) in Japanese allogeneic hematopoietic stem cell transplant (HSCT) recipients. Sixteen HSCT patients (8 patients each receiving tacrolimus or cyclosporine) were enrolled. An ITCZ oral solution was administered from day 30 after the initiation of ITCZ administration as a loading dose. Before the co-administration of ITCZ and CNI and 1 week daily thereafter, whole blood ITCZ and CNI (tacrolimus or cyclosporine) concentrations were measured in samples taken just before (C-0h) and 2 h (C-2h) after CNI administration. The median dose-adjusted C-0h values of tacrolimus and cyclosporine on day 7 after the start of ITCZ co-administration were 5.6- and 2.7-fold higher, respectively, than the corresponding values obtained before the initiation of ITCZ treatment. On day 7 after ITCZ treatment, the mean single dosages of tacrolimus and cyclosporine were reduced to 33.7 and 66.5 % of the dosages before ITCZ co-administration, respectively, to adjust the CNI target concentration. Although ITCZ co-administration did not alter the dose-adjusted C-0h values of tacrolimus in a patient with a CYP3A5*1/*1 allele, it did change this value of tacrolimus in patients with CYP3A5*3 alleles. However, in patients receiving cyclosporine, no such tendency was observed. The magnitude of the interaction between orally administered tacrolimus and ITCZ was significantly greater than that between cyclosporine and ITCZ. Prospective analysis of the CYP3A5 polymorphism may be important to ensure safe and reliable immunosuppressive therapy with tacrolimus in patients treated with ITCZ.
引用
收藏
页码:1321 / 1329
页数:9
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