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非肥胖成年血液恶性肿瘤患者行造血细胞移植时总兔抗胸腺细胞球蛋白的群体药代动力学。

Population Pharmacokinetics of Total Rabbit Anti-thymocyte Globulin in Non-obese Adult Patients Undergoing Hematopoietic Cell Transplantation for Hematologic Malignancy.

机构信息

Pediatric Stem Cell Transplantation, Boston Children's Hospital/Dana Farber Cancer Institute, Boston, MA, USA.

Department of Experimental and Clinical Pharmacology, University of Minnesota College of Pharmacy, Minneapolis, MN, USA.

出版信息

Clin Pharmacokinet. 2023 Aug;62(8):1081-1091. doi: 10.1007/s40262-023-01252-4. Epub 2023 Jun 7.

Abstract

BACKGROUND AND OBJECTIVES

Rabbit anti-thymocyte globulin (rATG), a therapeutic polyclonal antibody against human T cells, is commonly used in conditioning therapy prior to allogeneic hematopoietic cell transplantation (HCT). Previous studies successfully developed an individualized rATG dosing regimen based on "active" rATG population PK (popPK) analysis, while "total" rATG can be a more logistically favorable alternative for early HCT outcomes. We conducted a novel popPK analysis of total rATG.

METHODS

Total rATG concentration was measured in adult human-leukocyte antigen (HLA) mismatched HCT patients who received a low-dose rATG regimen (total 2.5-3 mg/kg) within 3 days prior to HCT. PopPK modeling and simulation was performed using nonlinear mixed effect modeling approach.

RESULTS

A total of 504 rATG concentrations were available from 105 non-obese patients with hematologic malignancy (median age 47 years) treated in Japan. The majority had acute leukemia or malignant lymphoma (94%). Total rATG PK was described by a two-compartment linear model. Influential covariate relations include ideal body weight [positively on both clearance (CL) and central volume of distribution], baseline serum albumin (negatively on CL), CD4 T cell dose (positively on CL), and baseline serum IgG (positively on CL). Simulated covariate effects predicted that early total rATG exposures were affected by ideal body weight.

CONCLUSIONS

This novel popPK model described the PK of total rATG in the adult HCT patients who received a low-dose rATG conditioning regimen. This model can be used for model-informed precision dosing in the settings with minimal baseline rATG targets (T cells), and early clinical outcomes are of interest.

摘要

背景与目的

兔抗胸腺细胞球蛋白(rATG)是一种针对人 T 细胞的治疗性多克隆抗体,常用于异基因造血细胞移植(HCT)前的预处理。先前的研究成功地基于“活性”rATG 群体药代动力学(popPK)分析开发了个体化 rATG 剂量方案,而“总”rATG 可能是早期 HCT 结果更具逻辑优势的替代方案。我们对总 rATG 进行了新的 popPK 分析。

方法

在接受 HLA 错配 HCT 的成人患者中,在 HCT 前 3 天内接受低剂量 rATG 方案(总剂量 2.5-3mg/kg),测量其总 rATG 浓度。使用非线性混合效应模型方法进行 popPK 建模和模拟。

结果

来自日本 105 例非肥胖血液恶性肿瘤患者(中位年龄 47 岁)的 504 个 rATG 浓度可用。大多数患者患有急性白血病或恶性淋巴瘤(94%)。总 rATG PK 由两室线性模型描述。有影响的协变量关系包括理想体重[对清除率(CL)和中央分布容积均呈正影响]、基线血清白蛋白(对 CL 呈负影响)、CD4 T 细胞剂量(对 CL 呈正影响)和基线血清 IgG(对 CL 呈正影响)。模拟的协变量效应预测,理想体重会影响早期总 rATG 暴露量。

结论

该新型 popPK 模型描述了接受低剂量 rATG 预处理方案的成人 HCT 患者的总 rATG PK。该模型可用于在基线 rATG 靶标(T 细胞)最小的情况下进行模型指导的精准剂量调整,并且早期临床结果是我们感兴趣的。

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