Takeuchi Masato, Yano Ikuko, Ito Satoko, Sugimoto Mitsuhiro, Yamamoto Shota, Yonezawa Atsushi, Ikeda Akio, Matsubara Kazuo
*Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, Kyoto, Japan; †Department of Clinical Pharmacy and Education, Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan; ‡Department of Pharmacy, Kobe University Hospital, Kobe; and §Department of Epilepsy, Movement Disorders and Physiology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Ther Drug Monit. 2017 Apr;39(2):124-131. doi: 10.1097/FTD.0000000000000383.
Topiramate is a second-generation antiepileptic drug used as monotherapy and adjunctive therapy in adults and children with partial seizures. A population pharmacokinetic (PPK) analysis was performed to improve the topiramate dosage adjustment for individualized treatment.
Patients whose steady-state serum concentration of topiramate was routinely monitored at Kyoto University Hospital from April 2012 to March 2013 were included in the model-building data. A nonlinear mixed effects modeling program was used to evaluate the influence of covariates on topiramate pharmacokinetics. The obtained PPK model was evaluated by internal model validations, including goodness-of-fit plots and prediction-corrected visual predictive checks, and was externally confirmed using the validation data from January 2015 to December 2015.
A total of 177 steady-state serum concentrations from 93 patients were used for the model-building analysis. The patients' age ranged from 2 to 68 years, and body weight ranged from 8.6 to 105 kg. The median serum concentration of topiramate was 1.7 mcg/mL, and half of the patients received carbamazepine coadministration. Based on a one-compartment model with first order absorption and elimination, the apparent volume of distribution was 105 L/70 kg, and the apparent clearance was allometrically related to the body weight as 2.25 L·h·70 kg without carbamazepine or phenytoin. Combination treatment with carbamazepine or phenytoin increased the apparent clearance to 3.51 L·h·70 kg. Goodness-of-fit plots, prediction-corrected visual predictive check, and external validation using the validation data from 43 patients confirmed an appropriateness of the final model. Simulations based on the final model showed that dosage adjustments allometrically scaling to body weight can equalize the serum concentrations in children of various ages and adults.
The PPK model, using the power scaling of body weight, effectively elucidated the topiramate serum concentration profile ranging from pediatric to adult patients. Dosage adjustments based on body weight and concomitant antiepileptic drug help obtain the dosage of topiramate necessary to reach an effective concentration in each individual.
托吡酯是一种第二代抗癫痫药物,用于成人和儿童部分性癫痫发作的单药治疗和辅助治疗。进行了群体药代动力学(PPK)分析,以改善托吡酯的剂量调整,实现个体化治疗。
将2012年4月至2013年3月在京都大学医院常规监测托吡酯稳态血清浓度的患者纳入模型构建数据。使用非线性混合效应建模程序评估协变量对托吡酯药代动力学的影响。通过内部模型验证(包括拟合优度图和预测校正视觉预测检查)对获得的PPK模型进行评估,并使用2015年1月至2015年12月的验证数据进行外部确认。
共将93例患者的177个稳态血清浓度用于模型构建分析。患者年龄范围为2至68岁,体重范围为8.6至105 kg。托吡酯的血清浓度中位数为1.7 mcg/mL,一半患者同时服用卡马西平。基于具有一级吸收和消除的单室模型,分布表观容积为105 L/70 kg,在未服用卡马西平或苯妥英钠时,表观清除率与体重呈异速生长关系,为2.25 L·h·70 kg。与卡马西平或苯妥英钠联合治疗可使表观清除率增加至3.51 L·h·70 kg。拟合优度图、预测校正视觉预测检查以及使用43例患者的验证数据进行的外部验证均证实了最终模型的适宜性。基于最终模型的模拟显示,根据体重进行异速生长比例的剂量调整可使不同年龄儿童和成人的血清浓度相等。
使用体重幂次缩放的PPK模型有效地阐明了从儿科到成人患者的托吡酯血清浓度分布情况。基于体重和联合使用的抗癫痫药物进行剂量调整有助于获得托吡酯在每个个体中达到有效浓度所需的剂量。