Eltrombopag treatment in thrombocytopenia following hematopoietic stem cell transplantation: A multicenter real-world experience

IF 2.1 4区 医学 Q3 HEMATOLOGY Leukemia research Pub Date : 2024-03-15 DOI:10.1016/j.leukres.2024.107484
Ebru Kilic Gunes , Sureyya Yigit Kaya , Fatih Yaman , Mustafa Kemal Yeniay , Kurtulus Vural , Melda Comert , Omur Gokmen Sevindik , Neslihan Andic , Simten Dagdas , Ilknur Nizam Ozen , Leylagul Kaynar , Filiz Yavasoglu , Gulsum Ozet , Volkan Karakus , Meltem Ayli
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Abstract

Introduction

Thrombocytopenia is among the most common complications following hematopoietic stem cell transplantation and is associated with increased mortality and morbidity with no standard treatment yet. In this multicenter and retrospective study, we aim to present our multi-center experience of Eltrombopag treatment in patients with isolated thrombocytopenia following HSCT.

Material-method

A total of 73 patients from 5 centers who underwent autologous or allogeneic stem cell transplantation, had no primary disease relapse, all of whom had neutrophil engraftment, complete chimerism, and who were diagnosed with Prolonged Isolated Thrombocytopenia (PIT) or Secondary Failure Of Platelet Recovery (SFPR) were included in the study. The patients were initiated on Eltrombopag at a dose of 50–150 mg. Complete response was defined as a platelet count >50×109/L for 7 consecutive days with no transfusion support.

Results

A total of 50.3% of the patients underwent Autologous and 49.7% Allogeneic Stem Cell Transplantation, 54.8% were diagnosed with PIT, and 45.2% were diagnosed with SFPR, and the treatment with 50–150 mg/day Eltrombopag was initiated on the median day +42. Complete response was achieved in 71.2% of these patients on the median day 23 of the treatment. No significant effects of the initial dose (50–150 mg/day) were detected in the Complete Response in the multivariate analysis on response. An insufficient number of Megakaryocytes in the bone marrow before Eltrombopag treatment was determined as an independent risk factor in determining the response (OR 3.57, 95% CI 1.21–10.55). The overall survival of the patients who did not respond to Eltrombopag was found to be significantly worse than that of patients who responded (p=0.022, HR:2.74, 95% CI 1.12–6.54).

Conclusion

As a result of the present study, Eltrombopag treatment was found to be effective and safe in thrombocytopenia that develops following hematopoietic stem cell transplantation. It was concluded that its use may be more effective in patients with sufficient bone marrow megakaryocytes before the treatment and an initial dose of 50 mg/day may be appropriate in terms of cost, effectiveness, and toxicity. Large-scale randomized and controlled prospective studies are needed to determine the roles of Eltrombopag treatment in patients with post-transplant PIT and SFPR.

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造血干细胞移植后血小板减少症的 Eltrombopag 治疗:多中心真实世界经验
血小板减少症是造血干细胞移植后最常见的并发症之一,与死亡率和发病率增加有关,目前尚无标准治疗方法。在这项多中心回顾性研究中,我们旨在介绍造血干细胞移植后孤立性血小板减少症患者使用艾曲波帕治疗的多中心经验。研究共纳入了来自 5 个中心的 73 名患者,他们接受了自体或异体干细胞移植,没有原发疾病复发,所有患者都有中性粒细胞移植、完全嵌合,并被诊断为长期孤立性血小板减少症(PIT)或继发性血小板恢复失败(SFPR)。患者开始使用 Eltrombopag,剂量为 50-150 毫克。完全应答的定义是血小板计数连续 7 天大于 50×10/L,且无需输血支持。共有 50.3% 的患者接受了自体干细胞移植,49.7% 的患者接受了异体干细胞移植,54.8% 的患者被诊断为 PIT,45.2% 的患者被诊断为 SFPR。其中71.2%的患者在治疗的中位第23天获得了完全应答。在对反应进行多变量分析时,未发现初始剂量(50-150 毫克/天)对完全反应有明显影响。艾曲波帕治疗前骨髓中巨核细胞数量不足被认为是决定反应的一个独立风险因素(OR 3.57,95% CI 1.21-10.55)。研究发现,对艾曲波帕治疗无反应的患者的总生存率明显低于有反应的患者(P=0.022,HR:2.74,95% CI 1.12-6.54)。本研究发现,艾曲波帕对造血干细胞移植后出现的血小板减少症有效且安全。结论是,在治疗前骨髓巨核细胞充足的患者中使用艾曲波帕可能更有效,而且从成本、有效性和毒性方面考虑,50 毫克/天的初始剂量可能是合适的。需要进行大规模的随机对照前瞻性研究,以确定 Eltrombopag 治疗在移植后 PIT 和 SFPR 患者中的作用。
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
Leukemia research
Leukemia research 医学-血液学
CiteScore
4.00
自引率
3.70%
发文量
259
审稿时长
1 months
期刊介绍: Leukemia Research an international journal which brings comprehensive and current information to all health care professionals involved in basic and applied clinical research in hematological malignancies. The editors encourage the submission of articles relevant to hematological malignancies. The Journal scope includes reporting studies of cellular and molecular biology, genetics, immunology, epidemiology, clinical evaluation, and therapy of these diseases.
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