Eltrombopag促进造血细胞移植后因移植物功能差而导致的细胞减少的恢复。

Blood cell therapy Pub Date : 2025-01-24 eCollection Date: 2025-02-25 DOI:10.31547/bct-2024-017
Khalid Halahleh, Maram Al-Ya'Goub, Mohamad Ma'koseh, Rozan Al-Far, Waleed Da'na, Rula Al-Najjar Pharm, Ayat Taqash, Isra Muradi, Maher Sughayer, Husam Abu-Jazar
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引用次数: 0

摘要

移植功能差(PrGF)是同种异体造血细胞移植(allogeneic hematopoietic cell transplantation, allo-HCT)的一个严重并发症,目前的治疗方法仅部分有效。8篇发表的关于eltrombopag对PrGF影响的报告显示了令人鼓舞的结果。本研究旨在评估eltrombopag治疗同种异体造血干细胞移植后PrGF的安全性和有效性。方法:对2013年1月至2023年12月在约旦安曼侯赛因国王癌症中心(KHCC)接受同种异体细胞移植后PrGF治疗的23例患者进行回顾性研究。患者、疾病和移植相关的特征从KHCC-BMT数据库中获得。结果:中位年龄47岁(范围26 ~ 68岁),女性13例。14名患者接受了低强度调节,14名供体是人类白细胞抗原(HLA)相同的兄弟姐妹。给药前血红蛋白(Hb)的中位浓度为8.5 g/dL(范围:6-14.2 g/dL),粒细胞为7.1 × 109/L(范围:1.6-85 × 109/L),血小板为18 × 109/L(范围:6-50 × 109/L)。血小板< 20 × 109/L 13例,巨核细胞减少15例。cd34阳性细胞中位剂量为6.10 × 106/kg(范围:2.75 ~ 9.78 × 106/kg)。Eltrombopag在移植后中位105天(d)(范围:29-800 d)开始使用,中位每周剂量为488 mg(范围:350-700 mg),中位治疗持续时间为75 d(范围:5-446 d)。总的来说,65%的患者(n=15)在中位30 d(范围:7-122 d)出现应答,12名应答者在中位随访30个月(范围:7.0-122个月)时存活,血液计数正常。2年总生存率为48%(95%可信区间,27-70%),7例无应答者因复发死亡。无重大不良事件报告。结论:Eltrombopag改善了同种异体hct后PrGF患者的外周血计数。因此,对eltrombopag的反应是可预测的,并且对生存有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Eltrombopag Enhances Recovery from Cytopenias Due to Poor Graft Function after Hematopoietic Cell Transplantation.

Eltrombopag Enhances Recovery from Cytopenias Due to Poor Graft Function after Hematopoietic Cell Transplantation.

Eltrombopag Enhances Recovery from Cytopenias Due to Poor Graft Function after Hematopoietic Cell Transplantation.

Eltrombopag Enhances Recovery from Cytopenias Due to Poor Graft Function after Hematopoietic Cell Transplantation.

Introduction: Poor graft function (PrGF) is a serious complication of allogeneic hematopoietic cell transplantation (allo-HCT), and current therapies are only partially effective. Eight published reports on the effect of eltrombopag on PrGF showed encouraging results. This study aimed to assess the safety and efficacy of eltrombopag for the treatment of PrGF after allo-HCT.

Methods: A retrospective study was conducted on 23 patients with PrGF following allo-HCT at the King Hussein Cancer Center (KHCC), Amman, Jordan between January 2013 and December 2023. The patient-, disease-, and transplant-related characteristics were obtained from the KHCC-BMT database.

Results: The median age was 47 years (range, 26-68 years), and 13 patients were female. Fourteen patients received reduced-intensity conditioning, and 14 donors were human-leukocyte antigen (HLA) -identical siblings. Median hemoglobin (Hb) concentration pre-eltrombopag administration was 8.5 g/dL (range: 6-14.2 g/dL), granulocytes 7.1 × 109/L (range: 1.6-85 × 109/L), and platelets 18 × 109/L (range: 6-50 × 109/L). Thirteen patients had platelets < 20 × 109/L, and 15 had reduced megakaryocytes. The median CD34-positive cell dose was 6.10 × 106/kg (range: 2.75-9.78 × 106/kg). Eltrombopag was initiated at a median of 105 day (d) post-transplant (range: 29-800 d). The median weekly dose was 488 mg (range: 350-700 mg), and the median treatment duration was 75 d (range: 5-446 d). In total, 65% of patients (n=15) responded at a median of 30 d (range, 7-122 d). Twelve responders were alive at a median follow-up of 30 months (range: 7.0-122 months) with normal blood counts. The 2-year overall rate was 48% (95% confidence intervals, 27-70%), and seven non-responders died because of relapse. No major adverse events were reported.

Conclusion: Eltrombopag improved peripheral blood counts in patients with PrGF following allo-HCT. Thus, response to eltrombopag was predictable and has a significant effect on survival.

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