Jacobson Pamala, Rogosheske John, Barker Juliet N, Green Kathleen, Ng Juki, Weisdorf Daniel, Tan Ye, Long Janel, Remmel Rory, Sawchuk Ronald, McGlave Philip
Department of Experimental and Clinical Pharmacology, WDH 7-189, College of Pharmacy, University of Minnesota, 308 Harvard Street SE, Minneapolis, MN 55455, USA.
Clin Pharmacol Ther. 2005 Nov;78(5):486-500. doi: 10.1016/j.clpt.2005.08.009.
Mycophenolate mofetil is used increasingly to provide immunosuppression after nonmyeloablative allogeneic hematopoietic cell transplantation. There is wide variability in the pharmacokinetics of mycophenolic acid (MPA), the active metabolite, and low concentrations are associated with rejection after organ transplantation. We hypothesized that low MPA was associated with poorer engraftment and a higher incidence of acute graft versus host disease. We evaluated the pharmacokinetics in 87 adult subjects undergoing nonmyeloablative-related and nonmyeloablative-unrelated hematopoietic cell transplantation who were receiving 1 g mycophenolate mofetil orally or intravenously every 12 hours plus cyclosporine (INN, ciclosporin). Subjects with an unbound MPA area under the curve (AUC) from 0 to 6 hours of less than 150 ng . h/mL had a higher cumulative incidence of grade II-IV acute graft versus host disease than subjects with a greater AUC (68% versus 40%, P = .02). An unbound AUC from 0 to 12 hours of less than 300 ng . h/mL was also associated with more frequent acute graft versus host disease (58% versus 35%, P = .05). There was no association between graft versus host disease and trough concentrations (P < or = .62). A higher cumulative incidence of engraftment was associated with total MPA trough concentrations greater than 1 microg/mL (P < .01). All engraftment failures occurred in the cord blood recipients. About one half of subjects were below the unbound AUC target after oral dosing with nearly a 5-fold variability in AUC. Intravenous dosing achieved unbound targets better than oral dosing. The current practice of dosing with 1 g twice daily provides inadequate plasma concentrations in many patients, and doses of at least 3 g/d are likely necessary. Therapeutic monitoring of MPA concentrations with dose adjustment into the therapeutic target appears to be necessary for the most effective use of mycophenolate mofetil.
霉酚酸酯越来越多地用于非清髓性异基因造血细胞移植后的免疫抑制。活性代谢产物霉酚酸(MPA)的药代动力学存在很大差异,低浓度与器官移植后的排斥反应相关。我们假设低MPA与植入较差及急性移植物抗宿主病的发生率较高有关。我们评估了87例接受非清髓性相关和非清髓性无关造血细胞移植的成年受试者的药代动力学,这些受试者每12小时口服或静脉注射1 g霉酚酸酯并加用环孢素(国际非专利药品名称,环孢菌素)。0至6小时未结合MPA曲线下面积(AUC)小于150 ng·h/mL的受试者,其II-IV级急性移植物抗宿主病的累积发生率高于AUC较高的受试者(68%对40%,P = 0.02)。0至12小时未结合AUC小于300 ng·h/mL也与更频繁的急性移植物抗宿主病相关(58%对35%,P = 0.05)。移植物抗宿主病与谷浓度之间无关联(P≤0.62)。总MPA谷浓度大于1μg/mL与较高的植入累积发生率相关(P < 0.01)。所有植入失败均发生在脐血受者中。口服给药后约一半受试者未达到未结合AUC目标,AUC存在近5倍的差异。静脉给药比口服给药更能达到未结合目标。目前每日两次1 g给药的做法在许多患者中血浆浓度不足,可能需要至少3 g/d的剂量。为最有效地使用霉酚酸酯,对MPA浓度进行治疗监测并根据剂量调整至治疗目标似乎是必要的。