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西罗莫司在卡波西样血管内皮瘤儿科患者中的群体药代动力学:一项回顾性研究。

Population pharmacokinetics of sirolimus in pediatric patients with kaposiform hemangioendothelioma: A retrospective study.

作者信息

Wang Dongdong, Chen Xiao, Li Zhiping

机构信息

Department of Pharmacy, Children's Hospital of Fudan University, Shanghai 201102, P.R. China.

Department of Pharmacy, The People's Hospital of Jiangyin, Jiangyin, Jiangsu 214400, P.R. China.

出版信息

Oncol Lett. 2019 Sep;18(3):2412-2419. doi: 10.3892/ol.2019.10562. Epub 2019 Jul 4.

DOI:10.3892/ol.2019.10562
PMID:31452734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6676569/
Abstract

Numerous studies have established population pharmacokinetics (PPK) models of sirolimus in various populations. However, a PPK model of sirolimus in Chinese patients with pediatric kaposiform hemangioendothelioma (PKHE) has yet to be established; therefore, this was the purpose of the present study. The present study was a retrospective analysis that utilized the trough concentration data obtained from traditional therapeutic drug monitoring-based dose adjustments. A total of 17 Chinese patients with PKHE from a real-world study were characterized by non-linear mixed-effects modeling. The impact of demographic features, biological characteristics and concomitant medications was assessed. The developed final model was evaluated via bootstrap and a prediction-corrected visual predictive check. A one-compartment model with first-order absorption and elimination was used for modeling of data for PKHE. The typical values of apparent oral clearance (CL/F) and apparent volume of distribution (V/F) in the final model were 3.19 l/h and 165 liters, respectively. Age, alanine transaminase levels and sex were included as significant covariates for CL/F, while the duration of treatment with sirolimus was a significant covariate for V/F. In conclusion, the present study developed and validated the first sirolimus PPK model for Chinese patients with PKHE.

摘要

众多研究已建立了西罗莫司在不同人群中的群体药代动力学(PPK)模型。然而,中国小儿卡波西样血管内皮瘤(PKHE)患者的西罗莫司PPK模型尚未建立;因此,本研究旨在建立该模型。本研究是一项回顾性分析,利用了基于传统治疗药物监测的剂量调整所获得的谷浓度数据。通过非线性混合效应模型对来自一项真实世界研究的17例中国PKHE患者进行了特征分析。评估了人口统计学特征、生物学特征和合并用药的影响。通过自抽样法和预测校正视觉预测检查对所建立的最终模型进行了评估。采用具有一级吸收和消除的单室模型对PKHE的数据进行建模。最终模型中表观口服清除率(CL/F)和表观分布容积(V/F)的典型值分别为3.19升/小时和165升。年龄、丙氨酸转氨酶水平和性别被纳入为CL/F的显著协变量,而西罗莫司的治疗持续时间是V/F的显著协变量。总之,本研究建立并验证了首个针对中国PKHE患者的西罗莫司PPK模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/ae1481c8514c/ol-18-03-2412-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/928b93dcc32c/ol-18-03-2412-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/2cf4b6eb646e/ol-18-03-2412-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/1fb555d5a4fa/ol-18-03-2412-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/ae1481c8514c/ol-18-03-2412-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/928b93dcc32c/ol-18-03-2412-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/2cf4b6eb646e/ol-18-03-2412-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/1fb555d5a4fa/ol-18-03-2412-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ae/6676569/ae1481c8514c/ol-18-03-2412-g03.jpg

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