Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Clinical Pharmacokinetics and Pharmacodynamics Unit, King Saud University Medical City, Riyadh, Saudi Arabia.
Int J Clin Pharm. 2020 Apr;42(2):703-712. doi: 10.1007/s11096-020-00989-3. Epub 2020 Mar 5.
Background Busulfan is an antineoplastic drug that is used widely as part of a conditioning regimen in pediatric patients undergoing hematopoietic stem cell transplantation. It has a narrow therapeutic index and highly variable pharmacokinetics; therefore therapeutic drug monitoring is recommended to optimize busulfan dosing. Objective To study the population pharmacokinetics of busulfan in Saudi pediatric patients to optimize its dosing. Settings King Abdullah Specialist Children's Hospital in Riyadh, Saudi Arabia. Methods This pharmacokinetic observational study was conducted between January 2016 and December 2018. All pediatric patients receiving IV busulfan and undergoing routine therapeutic drug monitoring were included. Population pharmacokinetics modeling was conducted using Monolix2019R1. Pharmacokinetic data of busulfan in children. Results The study included 59 patients and 513 samples. The mean ± SD age was 6.10 ± 3.17 years, and the dose administered was 0.994 ± 0.15 mg/kg. The mean ± SD Cmax and area under the curve (AUC) were 900.60 ± 402.8 ng/mL and 1031.14 ± 300.75 µM min, respectively. Based on our simulations, the European Medicines Agency recommended dose were adequate for most patient's groups to achieve the conventional target of an AUC of 900-1350 µM min. For patients in the lower weight group < 9 kg, higher doses were need at 1.2 mg/kg. With regards to the newly proposed target of AUC 78-101 mg h/mL, all of the doses we tested had low probability of achieving it. Conclusions Most of our patients had less than a proportional increase in busulfan concentration suggesting autoinduction. The high interindividual variability and autoinduction make dose adjustments challenging and AUC at steady state difficult to predict from the first dose. One approach to improve dose predictions is to use Bayesian dosing software. Based on our simulations, the European Medicines Agency recommended doses were adequate for most patient groups, except those in the lower (< 9 kg) and higher weight groups (> 34 kg).
背景 白消安是一种抗肿瘤药物,广泛用于儿科患者造血干细胞移植的预处理方案中。它的治疗指数狭窄,药代动力学变化很大;因此,建议进行治疗药物监测以优化白消安的剂量。目的 研究沙特儿科患者白消安的群体药代动力学,以优化其剂量。地点 沙特阿拉伯利雅得阿卜杜拉国王专科儿童医院。方法 这项药代动力学观察性研究于 2016 年 1 月至 2018 年 12 月进行。所有接受静脉注射白消安并进行常规治疗药物监测的儿科患者均纳入研究。使用 Monolix2019R1 进行群体药代动力学建模。白消安在儿童中的药代动力学数据。结果 该研究纳入了 59 名患者和 513 个样本。患者的平均年龄为 6.10±3.17 岁,给予的剂量为 0.994±0.15mg/kg。平均 Cmax 和 AUC 分别为 900.60±402.8ng/mL 和 1031.14±300.75µM·min。根据我们的模拟,欧洲药品管理局推荐的剂量对于大多数患者群体来说是足够的,可以达到 AUC 为 900-1350µM·min 的常规目标。对于体重小于 9kg 的较低体重组患者,需要更高的剂量 1.2mg/kg。对于新提出的 AUC 78-101mg·h/mL 的目标,我们测试的所有剂量都不太可能达到。结论 我们的大多数患者的白消安浓度增加不成比例,提示自动诱导。个体间的高度变异性和自动诱导使得剂量调整具有挑战性,稳态时的 AUC 也难以从首次剂量预测。一种改善剂量预测的方法是使用贝叶斯给药软件。根据我们的模拟,欧洲药品管理局推荐的剂量对于大多数患者群体是足够的,除了那些体重较低(<9kg)和较高(>34kg)的患者群体。