Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma

Sirolimus is an effective oral treatment for pediatric patients with lymphangioma. The present clinical study in 15 children (0.12–16.39 years of age) examines the effects of underlying factors on sirolimus concentrations through application of a population pharmacokinetic model. Using Monte Carlo s...

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Main Authors: Xiao Chen, Dongdong Wang, Guangfei Wang, Yidie Huang, Xin Yu, Jinmiao Lu, Xiaowen Zhai, Hong Xu, Zhiping Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-11-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.668952/full
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author Xiao Chen
Dongdong Wang
Guangfei Wang
Yidie Huang
Xin Yu
Jinmiao Lu
Xiaowen Zhai
Hong Xu
Zhiping Li
author_facet Xiao Chen
Dongdong Wang
Guangfei Wang
Yidie Huang
Xin Yu
Jinmiao Lu
Xiaowen Zhai
Hong Xu
Zhiping Li
author_sort Xiao Chen
collection DOAJ
description Sirolimus is an effective oral treatment for pediatric patients with lymphangioma. The present clinical study in 15 children (0.12–16.39 years of age) examines the effects of underlying factors on sirolimus concentrations through application of a population pharmacokinetic model. Using Monte Carlo simulation, an initial dose regimen for sirolimus in pediatric patients with lymphangioma is presented. It is found that the lower the body weight, the higher the clearance rate and sirolimus clearances are 0.31–0.17 L/h/kg in pediatric patients with lymphangioma whose weights are 5–60 kg, respectively. The doses of sirolimus, 0.07, 0.06, 0.05 mg/kg/day are recommended for weights of 5–10, 10–24.5 and 24.5–60 kg in children with lymphangioma. This study is the first to establish a population pharmacokinetic model for sirolimus and to recommend initial doses in pediatric patients with lymphangioma. Large scale, prospective studies are needed in the future.
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spelling doaj.art-c13e6d3278264d2a93c807a78e5b9a712022-12-21T18:01:58ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-11-011210.3389/fphar.2021.668952668952Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With LymphangiomaXiao Chen0Dongdong Wang1Guangfei Wang2Yidie Huang3Xin Yu4Jinmiao Lu5Xiaowen Zhai6Hong Xu7Zhiping Li8Department of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Hematology and Oncology, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Nephrology, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaDepartment of Pharmacy, National Children’s Medical Center, Children’s Hospital of Fudan University, Shanghai, ChinaSirolimus is an effective oral treatment for pediatric patients with lymphangioma. The present clinical study in 15 children (0.12–16.39 years of age) examines the effects of underlying factors on sirolimus concentrations through application of a population pharmacokinetic model. Using Monte Carlo simulation, an initial dose regimen for sirolimus in pediatric patients with lymphangioma is presented. It is found that the lower the body weight, the higher the clearance rate and sirolimus clearances are 0.31–0.17 L/h/kg in pediatric patients with lymphangioma whose weights are 5–60 kg, respectively. The doses of sirolimus, 0.07, 0.06, 0.05 mg/kg/day are recommended for weights of 5–10, 10–24.5 and 24.5–60 kg in children with lymphangioma. This study is the first to establish a population pharmacokinetic model for sirolimus and to recommend initial doses in pediatric patients with lymphangioma. Large scale, prospective studies are needed in the future.https://www.frontiersin.org/articles/10.3389/fphar.2021.668952/fulloptimizationinitial dose regimensirolimuspediatriclymphangioma
spellingShingle Xiao Chen
Dongdong Wang
Guangfei Wang
Yidie Huang
Xin Yu
Jinmiao Lu
Xiaowen Zhai
Hong Xu
Zhiping Li
Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma
Frontiers in Pharmacology
optimization
initial dose regimen
sirolimus
pediatric
lymphangioma
title Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma
title_full Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma
title_fullStr Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma
title_full_unstemmed Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma
title_short Optimization of Initial Dose Regimen for Sirolimus in Pediatric Patients With Lymphangioma
title_sort optimization of initial dose regimen for sirolimus in pediatric patients with lymphangioma
topic optimization
initial dose regimen
sirolimus
pediatric
lymphangioma
url https://www.frontiersin.org/articles/10.3389/fphar.2021.668952/full
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