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基于模型的精准剂量调整在儿科和年轻成年异体造血细胞移植患者中应用的阿仑单抗治疗。

Model-informed precision dosing for alemtuzumab in paediatric and young adult patients undergoing allogeneic haematopoietic cell transplantation.

机构信息

Division of Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.

出版信息

Br J Clin Pharmacol. 2022 Jan;88(1):248-259. doi: 10.1111/bcp.14955. Epub 2021 Jul 18.

Abstract

UNLABELLED

Alemtuzumab is a lymphodepleting monoclonal antibody utilized in conditioning regimens for allogeneic haematopoietic cell transplantation (HCT). A recently proposed therapeutic range of 0.15-0.6 μg/mL on the day of transplantation is associated with better HCT outcomes. The purpose of this study was to characterize alemtuzumab population pharmacokinetic/pharmacodynamic (PK/PD) and to propose individualized subcutaneous dosing schemes to achieve this optimal level for paediatric patients.

METHODS

Alemtuzumab concentration and absolute lymphocyte count (ALC) profiles were obtained from 29 paediatric and young adult patients (median age 6.4 y; range 0.28-21.4 y) with nonmalignant disorders undergoing HCT. PK/PD analyses were performed using nonlinear mixed effects modelling. Monte Carlo simulation was conducted to evaluate different improved dosing approaches.

RESULTS

A one-compartment model with sequential zero- and first-order absorption adequately described subcutaneously administered alemtuzumab PK. Model fit was significantly improved by including allometrically scaled body weight on clearance (0.080 L/h/70 kg) and volume of distribution (17.4 L/70 kg). ALC reduction following subcutaneous alemtuzumab was swift. An inhibitory E model best characterized the relationship between alemtuzumab concentration and ALC. E and EC were estimated as 1.18 × 10 /μL and 0.045 μg/mL, respectively. The currently used per kg dosing was found to cause uneven alemtuzumab exposure across different age and weight cohorts. Simulations indicated optimal target achieving dose as allometry-based dose of 18 mg × (weight/70) or body surface area-based dose of 10 mg/m , divided over 3 days, with a potential individualized top-up dose; both of which yielded similar results.

CONCLUSION

An allometry- or body surface area-based starting dosing regimen in combination with individualized Bayesian PK estimation using concentration feedback is proposed for alemtuzumab precision dosing in children undergoing allogeneic HCT.

摘要

目的

本研究旨在对阿仑单抗的群体药代动力学/药效学(PK/PD)进行特征分析,并提出个体化皮下给药方案,以达到儿科患者的最佳水平。

方法

对 29 例患有非恶性疾病的接受造血细胞移植(HCT)的儿科和年轻成年患者(中位年龄 6.4 岁;范围 0.28-21.4 岁)的阿仑单抗浓度和绝对淋巴细胞计数(ALC)谱进行了分析。采用非线性混合效应模型进行 PK/PD 分析。通过蒙特卡罗模拟来评估不同的改进给药方法。

结果

皮下给予阿仑单抗的 PK 可通过具有顺序零级和一级吸收的单室模型来很好地描述。通过将按比例缩放的体重纳入清除率(0.080 L/h/70 kg)和分布容积(17.4 L/70 kg),模型拟合得到了显著改善。皮下给予阿仑单抗后 ALC 的减少迅速。抑制 E 模型最好地描述了阿仑单抗浓度与 ALC 之间的关系。E 和 EC 分别估计为 1.18×10 /μL 和 0.045 μg/mL。目前使用的每公斤剂量在不同年龄和体重组之间会导致阿仑单抗暴露不均匀。模拟表明,最佳目标实现剂量为基于体质量的 18 mg×(体重/70)或基于体表面积的 10 mg/m ,分 3 天给予,可进行个体化的追加剂量;两者结果相似。

结论

建议对接受异体 HCT 的儿童采用基于体质量或体表面积的起始给药方案,并结合基于浓度反馈的个体化贝叶斯 PK 估算,以实现阿仑单抗的精准给药。

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