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首页> 外文期刊>Journal of oncology pharmacy practice: official publication of the International Society of Oncology Pharmacy Practitioners >Effect of aprepitant on intravenous tacrolimus disposition in reduced intensity hematopoietic stem cell transplantation.
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Effect of aprepitant on intravenous tacrolimus disposition in reduced intensity hematopoietic stem cell transplantation.

机译:阿瑞匹坦对降低强度的造血干细胞移植中他克莫司静脉配置的影响。

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摘要

Aprepitant (AP) is a known inhibitor of cytochrome P450 3A4 which may affect tacrolimus metabolism. We retrospectively examined the effect of oral AP on intravenous tacrolimus concentrations in 26 patients undergoing reduced intensity transplantation from 09/2005 to 09/2006. Oral AP 125 mg daily was administered on transplant day +1 and 80 mg on days +2 and +3. Intravenous tacrolimus was administered as a 0.03 mg/kg/day continuous infusion on day -6 through day +1 (pre-AP), during-AP (days +2 to +7), and post-AP starting on day +8. Tacrolimus doses were adjusted to achieve concentrations of 5-20 ng/mL. Dose-corrected tacrolimus concentrations (ng/mL/mg per dose) in the pre-AP, during-AP, and post-AP time periods were: 8.12 (95% CI: 7.3-9.1), 11.63 (95% CI: 9.63-13.63), and 11.42 (95% CI: 8.12-14.7), respectively (P<0.01 between pre-AP and during-AP, P<0.01 between during-AP and post-AP, P = 0.01 between pre-AP and post-AP time periods). Although statistically significant, the observed rise was not clinically significant between during-AP and post-AP time periods. Previous work has shown that AP is not expected to exert an inhibitory effect within 48 h of AP discontinuation. Collectively, these data suggest that AP effect on tacrolimus metabolism is of minor clinical significance. A controlled trial is needed to confirm these findings.
机译:阿瑞匹坦(AP)是一种已知的细胞色素P450 3A4抑制剂,可能会影响他克莫司的代谢。我们回顾性研究了从09/2005到09/2006,口服AP对26例接受降低强度移植的患者静脉他克莫司浓度的影响。在移植的第1天每天口服125 mg AP,在移植的第2天和+3天每天口服80 mg。在第-6天至第+1天(AP前),AP期间(+2至+7天)和AP后+8天开始以0.03 mg / kg /天的剂量连续静脉注射他克莫司。调整他克莫司的剂量以达到5-20 ng / mL的浓度。在AP之前,AP期间和AP之后的时间段中,剂量校正后的他克莫司浓度(ng / mL / mg /剂)分别为:8.12(95%CI:7.3-9.1),11.63(95%CI:9.63) -13.63)和11.42(95%CI:8.12-14.7)(AP前和AP期间P <0.01,AP期间和AP后P <0.01,AP之前和AP之间P = 0.01后AP时间段)。尽管有统计学意义,但观察到的上升在AP期间和AP之后的时间段之间并不具有临床意义。先前的工作表明,AP停药后48小时内预期不会发挥抑制作用。总的来说,这些数据表明AP对他克莫司代谢的作用具有较小的临床意义。需要进行对照试验以确认这些发现。

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