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通过甲氨蝶呤群体药代动力学模型预测骨肉瘤患者的亚叶酸钙解救治疗

Anticipating Leucovorin Rescue Therapy in Patients with Osteosarcoma through Methotrexate Population Pharmacokinetic Model.

作者信息

Olivo Laura Ben, de Oliveira Henz Pricilla, Wermann Sophia, Dias Bruna Bernar, Porto Gabriel Osorio, Pinhatti Amanda Valle, Martins Manoela Domingues, Gregianin Lauro José, Costa Teresa Dalla, de Araújo Bibiana Verlindo

机构信息

Pharmacokinetics and PK/PD Modeling Laboratory, Pharmaceutical Sciences Graduate Program, Federal University of Rio Grande do Sul, 2752 Ipiranga Ave., Santana, Porto Alegre 90610-000, RS, Brazil.

Medical Sciences Graduate Program, Federal University of Rio Grande do Sul, Porto Alegre 90610-000, RS, Brazil.

出版信息

Pharmaceutics. 2024 Sep 6;16(9):1180. doi: 10.3390/pharmaceutics16091180.

Abstract

Methotrexate (MTX), which presents high inter-individual variability, is part of the Brazilian Osteosarcoma Treatment Group (BOTG) protocol. This work aimed to develop a MTX population pharmacokinetic model (POPPK) for Brazilian children with osteosarcoma (OS) following the BOTG protocol to guide rescue therapy and avoid toxicity. The model was developed in NONMEM 7.4 (Icon) using retrospective sparse data from MTX therapeutic drug monitoring of children attending a southern Brazilian public reference hospital. Data were described by a two-compartment model using 216 MTX cycles from 32 patients (5-18 y.o.) with OS who received 12 g/m dose/cycle. To explain inter-individual and inter-occasion variability in clearance and peripheral volume, covariates from demographic and biochemical data were evaluated. Serum creatinine was a significant covariate of MTX clearance (14.8 L/h), and the body surface area (BSA) was significant for central compartment volume (82.5 L). Inter-compartmental clearance and volume of peripheral compartment were 0.178 L/h and 5.72 L, respectively. The model adequately describes MTX exposure in Brazilian children with OS. Successful simulations were performed to predict MTX concentrations in pediatric patients above five years old with acute kidney injury and anticipate rescue therapy adjustments.

摘要

甲氨蝶呤(MTX)个体间差异很大,是巴西骨肉瘤治疗组(BOTG)方案的一部分。这项研究旨在为遵循BOTG方案的巴西骨肉瘤(OS)患儿建立一个MTX群体药代动力学模型(POPPK),以指导救援治疗并避免毒性。该模型使用来自巴西南部一家公立参考医院接受MTX治疗药物监测的儿童的回顾性稀疏数据,在NONMEM 7.4(Icon)中开发。数据用两室模型描述,使用了32例(5 - 18岁)接受12 g/m剂量/周期的OS患者的216个MTX周期。为了解释清除率和外周容积的个体间和个体内变异性,评估了人口统计学和生化数据中的协变量。血清肌酐是MTX清除率(14.8 L/h)的显著协变量,体表面积(BSA)对中央室容积(82.5 L)有显著影响。室间清除率和外周室容积分别为0.178 L/h和5.72 L。该模型充分描述了巴西OS患儿的MTX暴露情况。成功进行了模拟,以预测五岁以上急性肾损伤儿科患者的MTX浓度,并预期救援治疗的调整。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6f8/11434990/013b3a593770/pharmaceutics-16-01180-g001.jpg

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