Department of Pharmacy, Shinshu University Hospital, Matsumoto, Japan.
Department of Biochemical Pharmacology and Toxicology, Graduate School of Medicine, Shinshu University, Matsumoto, Japan.
J Clin Pharm Ther. 2019 Aug;44(4):565-571. doi: 10.1111/jcpt.12834. Epub 2019 Apr 4.
Azole antifungal drugs are often co-administered with tacrolimus after allogeneic hematopoietic stem cell transplantation (HSCT). However, the influence of azole antifungal drugs on variation in tacrolimus pharmacokinetics when switching from intravenous tacrolimus (Tac-iv) to once-daily modified release tacrolimus (Tac-MR) remains to be elucidated. This study was performed to evaluate the effects of oral azole antifungal drugs on variation in tacrolimus pharmacokinetics after conversion to Tac-MR in HSCT patients.
Patients concomitantly receiving fluconazole (FLCZ) or voriconazole (VRCZ) along with tacrolimus were evaluated retrospectively. Blood tacrolimus concentrations before and after changing to oral administration were compared between FLCZ and VRCZ groups.
A total of 52 patients (34 FLCZ and 18 VRCZ) were included in the analysis. There were no significant differences in the most recent daily dose (D ) and blood level (C ) of Tac-iv, C /D , and ratio of daily dose of tacrolimus on the first to second day after changing to Tac-MR (D ) to D between FLCZ and VRCZ groups (P > 0.2). The trough levels of tacrolimus on the first to second day after switching to Tac-MR (C ) and on the third to fifth day after the switch (C ) were significantly higher in the VRCZ group than the FLCZ group (P < 0.05). The values of (C /D )/(C /D ) and (C /D )/(C /D ) in the VRCZ group were significantly lower compared with those in the FLCZ group (P < 0.05). Furthermore, individual values of (C /D )/(C /D ) in the FLCZ group varied widely.
Voriconazole increased blood tacrolimus level more markedly than FLCZ after switching to Tac-MR, whereas FLCZ caused a large variation in tacrolimus blood level. These results suggest that therapeutic monitoring of tacrolimus after the switch may need to be performed carefully considering that orally co-administered VRCZ and FLCZ exhibit different change in blood tacrolimus level just after the switch.
在异基因造血干细胞移植(HSCT)后,唑类抗真菌药物常与他克莫司联合使用。然而,从静脉用他克莫司(Tac-iv)转换为每日一次的改良释放他克莫司(Tac-MR)时,唑类抗真菌药物对他克莫司药代动力学变化的影响仍有待阐明。本研究旨在评估 HSCT 患者转换为 Tac-MR 后口服唑类抗真菌药物对他克莫司药代动力学变化的影响。
回顾性评估同时接受氟康唑(FLCZ)或伏立康唑(VRCZ)和他克莫司治疗的患者。比较 FLCZ 和 VRCZ 组在转换为口服给药前后的血他克莫司浓度。
共纳入 52 例患者(34 例 FLCZ 和 18 例 VRCZ)进行分析。两组间 Tac-iv 的最近每日剂量(D)和血药浓度(C)、C/D、转换为 Tac-MR 后第 1 至 2 天的每日剂量比(D)/D 无显著差异(P>0.2)。转换为 Tac-MR 后第 1 至 2 天(C)和第 3 至 5 天(C)的他克莫司谷浓度在 VRCZ 组显著高于 FLCZ 组(P<0.05)。VRCZ 组的(C/D)/(C/D)和(C/D)/(C/D)值明显低于 FLCZ 组(P<0.05)。此外,FLCZ 组的(C/D)/(C/D)个体值差异较大。
与 FLCZ 相比,伏立康唑在转换为 Tac-MR 后更显著地增加了血他克莫司水平,而 FLCZ 导致了血他克莫司水平的显著变化。这些结果表明,考虑到口服给予 VRCZ 和 FLCZ 后,血他克莫司水平在转换后即刻表现出不同的变化,转换后可能需要谨慎进行他克莫司的治疗监测。