Department of Pediatric Hematology and Oncology, Hospital Universitari Vall d´Hebron, Barcelona, Spain.
Department of Pharmacy, Hospital Universitari Vall d´Hebron, Barcelona, Spain.
Pediatr Transplant. 2021 Jun;25(4):e14010. doi: 10.1111/petr.14010. Epub 2021 Mar 20.
The main objective of this study was to determine whether Eltrombopag, a synthetic thrombopoietin receptor agonist, could improve peripheral blood counts in the three hematopoietic lineages and achieve transfusion independence in children with poor graft function (PGF) after allogenic hematopoietic stem cell transplantation (HSCT). Retrospective study of patients under 18 years who developed PGF post-HSCT in a large tertiary institution between January 2013 and March 2019. Out of 198 allogeneic HSCT, five patients met PGF criteria and were treated with eltrombopag. Median time from HSCT to eltrombopag initiation was 120 days. The median starting dose was 50 mg/day and the maximum dose reached was 75 mg/day. Median treatment duration was 9 months. Three patients achieved complete response and one partial response. The median dose among responders was 75 mg/day and the median time to response 8 weeks. Responses were sustained in three patients and two required a booster dose of CD34 -selected cells from the original donor. None of the patients had to stop treatment due to adverse effects. The use of eltrombopag in children with PGF achieved responses in 80% of cases and demonstrated to be an effective and safe therapeutic option in pediatric patients with PGF.
本研究的主要目的是确定合成的血小板生成素受体激动剂艾曲泊帕是否可以改善三种造血谱系的外周血计数,并使异基因造血干细胞移植(HSCT)后造血功能不良(PGF)的儿童实现输血独立性。回顾性研究了 2013 年 1 月至 2019 年 3 月在一家大型三级机构接受 HSCT 后发生 PGF 的 18 岁以下患者。在 198 例异基因 HSCT 中,有 5 例患者符合 PGF 标准并接受了艾曲泊帕治疗。从 HSCT 到艾曲泊帕起始治疗的中位时间为 120 天。起始剂量中位数为 50mg/天,最大剂量为 75mg/天。中位治疗持续时间为 9 个月。3 名患者获得完全缓解,1 名患者获得部分缓解。应答者的中位剂量为 75mg/天,中位应答时间为 8 周。3 名患者的应答持续存在,2 名患者需要从原始供体输注 CD34 选择的细胞来增强反应。由于不良反应,没有患者需要停止治疗。艾曲泊帕在 PGF 患儿中的应用,在 80%的病例中取得了应答效果,证明在儿科 PGF 患者中是一种有效且安全的治疗选择。