Department of Hematology, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita City, Akita 010-8543, Japan.
Eur J Clin Pharmacol. 2013 Jun;69(6):1321-9. doi: 10.1007/s00228-013-1471-2. Epub 2013 Jan 26.
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 (C0h) and 2 h (C2h) after CNI administration.
The median dose-adjusted C0h 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 C0h 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.
本研究旨在探讨伊曲康唑(ITCZ)与口服钙调磷酸酶抑制剂(CNI)在日本异基因造血干细胞移植(HSCT)受者中的相互作用。
纳入 16 例 HSCT 患者(每组 8 例分别接受他克莫司或环孢素治疗)。在开始 ITCZ 治疗后第 30 天给予 ITCZ 口服液作为负荷剂量。在开始联合应用 ITCZ 和 CNI 之前以及之后的每周 1 天,在 CNI 给药前(C0h)和给药后 2 小时(C2h)采集全血样本,测定 ITCZ 和 CNI(他克莫司或环孢素)的浓度。
在开始 ITCZ 联合治疗的第 7 天,与开始 ITCZ 治疗前相比,他克莫司和环孢素的剂量调整后 C0h 值分别升高了 5.6 倍和 2.7 倍。在 ITCZ 治疗后第 7 天,为调整 CNI 靶浓度,他克莫司和环孢素的平均单剂量分别减少至开始 ITCZ 联合治疗前的 33.7%和 66.5%。尽管 ITCZ 联合应用并未改变 CYP3A5 1/1 等位基因患者的他克莫司剂量调整后 C0h 值,但改变了 CYP3A5 3 等位基因患者的他克莫司的这一数值。然而,在接受环孢素的患者中,未观察到这种趋势。
口服他克莫司与 ITCZ 之间的相互作用程度明显大于环孢素与 ITCZ 之间的相互作用程度。对 CYP3A5 多态性的前瞻性分析可能对确保接受 ITCZ 治疗的患者使用他克莫司进行安全可靠的免疫抑制治疗非常重要。