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霉酚酸酯与标准剂量或减量他克莫司联合应用于肝移植受者的药代动力学、疗效及安全性

Pharmacokinetics, efficacy, and safety of mycophenolate mofetil in combination with standard-dose or reduced-dose tacrolimus in liver transplant recipients.

作者信息

Nashan Björn, Saliba Faouzi, Durand Francois, Barcéna Rafael, Herrero Jose Ignacio, Mentha Gilles, Neuhaus Peter, Bowles Matthew, Patch David, Bernardos Angel, Klempnauer Jürgen, Bouw René, Ives Jane, Mamelok Richard, McKay Diane, Truman Matt, Marotta Paul

机构信息

Department of Hepatobiliary Surgery and Visceral Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Liver Transpl. 2009 Feb;15(2):136-47. doi: 10.1002/lt.21657.

Abstract

The pharmacokinetics of mycophenolate mofetil (MMF) in liver transplant recipients may change because of pharmacokinetic interactions with coadministered immunosuppressants or because changes in the enterohepatic anatomy may affect biotransformation of MMF to mycophenolic acid (MPA) and enterohepatic recirculation of MPA through the hydrolysis of mycophenolate acid glucuronide to MPA in the gut. In the latter case, the choice of formulation (oral versus intravenous) could have important clinical implications. We randomized liver transplant patients (n = 60) to standard (10-15 ng/mL) or reduced (5-8 ng/mL) trough levels of tacrolimus plus intravenous MMF followed by oral MMF (1 g twice daily) with corticosteroids. Pharmacokinetic sampling was performed after the last intravenous MMF dose, after the first oral MMF dose, and at selected times over 52 weeks. The efficacy and safety of the 2 regimens were also assessed. Twenty-eight and 27 patients in the tacrolimus standard-dose and reduced-dose groups, respectively, were evaluated. No significant differences between the tacrolimus standard-dose and reduced-dose groups were seen in dose-normalized MPA values of the time to the maximum plasma concentration (1.25 versus 1.28 hours), the maximum plasma concentration (15.5 +/- 7.93 versus 13.6 +/- 7.03 microg/mL), or the area under the concentration-time curve from 0 to 12 hours (AUC(0-12); 53.0 +/- 20.6 versus 43.8 +/- 15.5 microg h/mL) at week 26 or at any other time point. No relationship was observed between the tacrolimus trough or AUC(0-12) and MPA AUC(0-12). Exposure to MPA after oral and intravenous administration was similar. Safety and efficacy were similar in the two treatment groups. In conclusion, exposure to MPA is not a function of exposure to tacrolimus. The similar safety and efficacy seen with MMF plus standard or reduced doses of tacrolimus suggest that MMF could be combined with reduced doses of tacrolimus.

摘要

肝移植受者中霉酚酸酯(MMF)的药代动力学可能会发生变化,这是因为与同时使用的免疫抑制剂存在药代动力学相互作用,或者因为肠肝解剖结构的改变可能会影响MMF向霉酚酸(MPA)的生物转化,以及MPA通过肠道中霉酚酸葡萄糖醛酸酯水解为MPA的肠肝循环。在后一种情况下,制剂的选择(口服与静脉注射)可能具有重要的临床意义。我们将肝移植患者(n = 60)随机分为接受标准(10 - 15 ng/mL)或降低(5 - 8 ng/mL)谷浓度的他克莫司加静脉注射MMF,随后口服MMF(每日两次,每次1 g)并联合使用皮质类固醇。在最后一次静脉注射MMF剂量后、第一次口服MMF剂量后以及52周内的选定时间进行药代动力学采样。还评估了两种治疗方案的疗效和安全性。他克莫司标准剂量组和降低剂量组分别有28例和27例患者接受了评估。在第26周或任何其他时间点,他克莫司标准剂量组和降低剂量组之间在剂量标准化的MPA值方面,如达最大血浆浓度时间(1.25对1.28小时)、最大血浆浓度(15.5±7.93对13.6±7.03μg/mL)或0至12小时浓度 - 时间曲线下面积(AUC(0 - 12);53.0±20.6对43.8±15.5μg·h/mL)方面均未观察到显著差异。未观察到他克莫司谷浓度或AUC(0 - 12)与MPA AUC(0 - 12)之间存在相关性。口服和静脉注射后MPA的暴露量相似。两个治疗组的安全性和疗效相似。总之,MPA的暴露量不是他克莫司暴露量的函数。MMF联合标准剂量或降低剂量的他克莫司所观察到的相似安全性和疗效表明,MMF可以与降低剂量的他克莫司联合使用。

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