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在儿童免疫性血小板减少症个体化治疗中建立艾曲泊帕预期浓度参考范围。

The establishment of an expected concentration reference range for eltrombopag in the individualized treatment of pediatric immune thrombocytopenia.

作者信息

Wang Nan, Dong Shuyue, Sun Yixin, Liu Jingjing, Wang Zhifa, Ma Jingyao, Wang Xiaoling, Wu Runhui, Cheng Xiaoling

机构信息

Department of Pharmacy, Beijing Children's Hospital, Capital Medical University, Beijing, China.

School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China.

出版信息

Front Pharmacol. 2025 Aug 21;16:1597641. doi: 10.3389/fphar.2025.1597641. eCollection 2025.

Abstract

BACKGROUND

Differences in the clinical efficacy and adverse drug reactions (ADRs) of eltrombopag (ELT) in children with immune thrombocytopenia (ITP) may be positively correlated with the serum trough concentration of ELT. Individual pharmacokinetic variations primarily contribute to differences in ELT concentration among individuals. This study is the first to establish an expected concentration reference range for ELT in treating pediatric persistent/chronic ITP (P/CITP) across different age-groups.

METHODS

A total of 94 patients with 111 serum trough concentrations were analyzed to validate this range. The median age of patients was 7.68 (5.35, 10.21) years, and 44.7% (42/49) of them were male.

RESULTS

Subgroup analyses revealed significant differences in ELT concentration related to the age, efficacy, and ADR occurrence. The expected concentration reference range was determined using the dose-related concentration (DRC) factor combined with the ELT dosage. The DRC factor ranges were as follows: 0.083-0.216 (mg/L)/mg in children aged 1-6 years, 0.058-0.125 (mg/L)/mg in children aged 7-12 years, and 0.043-0.097 (mg/L)/mg in children aged 13-18 years. Among patients with measured trough concentrations within the expected reference range, 84.3% (59/70) achieved response/complete response (R/CR) and 88.6% (62/70) did not experience ADR.

CONCLUSION

Serum trough concentration monitoring based on the established reference ranges could enhance the precision of individualized ELT therapy in pediatric ITP patients.

摘要

背景

艾曲泊帕(ELT)治疗免疫性血小板减少症(ITP)患儿的临床疗效及药物不良反应(ADR)差异可能与ELT血清谷浓度呈正相关。个体药代动力学差异是导致个体间ELT浓度不同的主要原因。本研究首次建立了ELT治疗不同年龄组小儿持续性/慢性ITP(P/CITP)的预期浓度参考范围。

方法

共分析94例患者的111个血清谷浓度以验证该范围。患者中位年龄为7.68(5.35,10.21)岁,其中44.7%(42/49)为男性。

结果

亚组分析显示ELT浓度在年龄、疗效及ADR发生方面存在显著差异。预期浓度参考范围通过剂量相关浓度(DRC)因子结合ELT剂量来确定。DRC因子范围如下:1 - 6岁儿童为0.083 - 0.216(mg/L)/mg,7 - 12岁儿童为0.058 - 0.125(mg/L)/mg,13 - 18岁儿童为0.043 - 0.097(mg/L)/mg。在预期参考范围内测得谷浓度的患者中,84.3%(59/70)达到反应/完全反应(R/CR),88.6%(62/70)未发生ADR。

结论

基于既定参考范围进行血清谷浓度监测可提高小儿ITP患者ELT个体化治疗的精准度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768f/12408700/e446f210e203/fphar-16-1597641-g001.jpg

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