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贝伐单抗在复发性脑肿瘤儿童和青少年中的脑脊液分布。

Distribution of Bevacizumab into the Cerebrospinal Fluid of Children and Adolescents with Recurrent Brain Tumors.

机构信息

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.

出版信息

Paediatr Drugs. 2024 Jul;26(4):429-440. doi: 10.1007/s40272-024-00624-y. Epub 2024 Apr 8.

DOI:10.1007/s40272-024-00624-y
PMID:38587585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11192692/
Abstract

BACKGROUND

To date, evidence has been lacking regarding bevacizumab pharmacokinetics in the cerebrospinal fluid (CSF).

OBJECTIVE

This study assessed the penetration of bevacizumab, as part of a metronomic antiangiogenic treatment regimen, into the CSF of children, adolescents, and young adults with recurrent brain tumors.

PATIENTS AND METHODS

Serum and CSF concentrations, malignant cells, and vascular endothelial growth factor A (VEGF-A) were analyzed in 12 patients (5-27 years) following 10 mg/kg bevacizumab intravenous biweekly administration (EudraCT number 2009-013024-23). A population pharmacokinetic model including body weight, albumin, and tumor type as influential factors was extended to quantify the CSF penetration of bevacizumab.

RESULTS

Apart from in serum (minimum concentration/maximum concentration [C/C] 77.0-305/267-612 mg/L, median 144/417 mg/L), bevacizumab could be quantified in the CSF (0.01-2.26 mg/L, median 0.35 mg/L). The CSF/serum ratio was 0.16 and highly variable between patients. Malignant cells could be detected in CSF before initiation of treatment in five of 12 patients; after treatment, the CSF was cleared in all patients. VEGF-A was detected in three patients before treatment (mean ± SD: 20 ± 11 pg/mL), and was still measurable in one of these patients despite treatment (16 pg/mL).

CONCLUSIONS

This pharmacokinetic pilot study indicated penetration of bevacizumab into the CSF in a population of children, adolescents, and young adults with recurrent brain tumors.

摘要

背景

迄今为止,有关贝伐单抗在脑脊液(CSF)中的药代动力学的证据尚缺乏。

目的

本研究评估贝伐单抗作为一种节拍式抗血管生成治疗方案的一部分,在复发性脑肿瘤的儿童、青少年和年轻成人中进入 CSF 的渗透情况。

患者和方法

在 12 例患者(5-27 岁)中,每两周静脉给予 10mg/kg 贝伐单抗(EudraCT 编号 2009-013024-23)后,分析血清和 CSF 浓度、恶性细胞和血管内皮生长因子 A(VEGF-A)。将包括体重、白蛋白和肿瘤类型作为影响因素的群体药代动力学模型进行扩展,以定量评估贝伐单抗进入 CSF 的情况。

结果

除了在血清中(最小浓度/最大浓度 [C/C] 77.0-305/267-612mg/L,中位数 144/417mg/L),贝伐单抗也可在 CSF 中定量(0.01-2.26mg/L,中位数 0.35mg/L)。CSF/血清比值为 0.16,且患者间差异很大。12 例患者中有 5 例在开始治疗前可检测到 CSF 中的恶性细胞,治疗后所有患者的 CSF 均得到清除。3 例患者在治疗前检测到 VEGF-A(平均值±标准差:20±11pg/mL),其中 1 例患者尽管进行了治疗,VEGF-A 仍可测量(16pg/mL)。

结论

这项药代动力学初步研究表明,贝伐单抗在复发性脑肿瘤的儿童、青少年和年轻成人中渗透进入 CSF。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/779e5f08b641/40272_2024_624_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/f39006d7d564/40272_2024_624_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/08d4e5aea791/40272_2024_624_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/cef1a326d41a/40272_2024_624_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/96c5eaf1dd02/40272_2024_624_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/a4c7891202e0/40272_2024_624_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/779e5f08b641/40272_2024_624_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/f39006d7d564/40272_2024_624_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/08d4e5aea791/40272_2024_624_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/cef1a326d41a/40272_2024_624_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/96c5eaf1dd02/40272_2024_624_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/a4c7891202e0/40272_2024_624_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/982d/11192692/779e5f08b641/40272_2024_624_Fig6_HTML.jpg

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