Update on the Use of Thrombopoietin-Receptor Agonists in Pediatrics.

IF 2.7 4区 医学 Q2 HEMATOLOGY
Hamostaseologie Pub Date : 2024-08-01 Epub Date: 2024-06-26 DOI:10.1055/a-2247-4209
Jennifer Gebetsberger, Werner Streif, Christof Dame
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Abstract

This review summarizes the rationale and current data on the use of thrombopoietin receptor agonists (TPO-RAs) for treating severe thrombocytopenia in infants, children, and adolescents. It focuses on substances that have been approved by the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) for pediatric patients. Romiplostim and eltrombopag are already established as second-line treatment for persistent or chronic immune thrombocytopenia (ITP). As in adults, TPO-RAs are currently also evaluated in severe aplastic anemia (SAA), chemotherapy-induced thrombocytopenia (CIT), myelodysplastic syndromes (MDS), and poor engraftment after hematopoietic stem cell transplantation in pediatric and adolescent patients. Moreover, studies on the implication of TPO-RA in treating rare inherited thrombocytopenias, such as Wiskott-Aldrich syndrome (WAS), congenital amegakaryocytic thrombocytopenia (CAMT), or MYH9-associated thrombocytopenia, deserve future attention. Current developments include testing of avatrombopag and lusutrombopag that are approved for the treatment of thrombocytopenia associated with chronic liver disease (CLD) in adult patients. In pediatric and adolescent medicine, we expect in the near future a broader use of TPO-RAs as first-line treatment in primary ITP, thereby considering immunomodulatory effects that increase the rate of sustained remission off-treatment, and a selective use in rare inherited thrombocytopenias based on current clinical trials.

儿科使用血小板生成素受体激动剂的最新情况。
本综述总结了使用促血小板生成素受体激动剂(TPO-RA)治疗婴儿、儿童和青少年严重血小板减少症的原理和当前数据。报告重点介绍美国食品药品管理局(FDA)和欧洲药品管理局(EMA)已批准用于儿科患者的药物。Romiplostim 和 eltrombopag 已被确定为治疗顽固性或慢性免疫性血小板减少症 (ITP) 的二线药物。与成人一样,TPO-RAs 目前也被评估用于重型再生障碍性贫血 (SAA)、化疗诱发血小板减少症 (CIT)、骨髓增生异常综合征 (MDS),以及儿科和青少年患者造血干细胞移植后接种不良的治疗。此外,TPO-RA在治疗罕见遗传性血小板减少症(如威斯科特-阿尔德里奇综合征(WAS)、先天性无巨核细胞血小板减少症(CAMT)或MYH9相关性血小板减少症)方面的作用研究也值得关注。目前的进展包括阿伐曲波帕和卢苏曲波帕的测试,这两种药物已被批准用于治疗成年患者慢性肝病(CLD)相关的血小板减少症。在儿童和青少年医学领域,我们预计在不久的将来,TPO-RAs 将被更广泛地用作原发性 ITP 的一线治疗,从而考虑到其免疫调节作用可提高治疗后的持续缓解率,并根据目前的临床试验有选择地用于罕见的遗传性血小板减少症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hamostaseologie
Hamostaseologie HEMATOLOGY-
CiteScore
5.50
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Hämostaseologie is an interdisciplinary specialist journal on the complex topics of haemorrhages and thromboembolism and is aimed not only at haematologists, but also at a wide range of specialists from clinic and practice. The readership consequently includes both specialists for internal medicine as well as for surgical diseases.
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