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在欧洲,艾曲波帕被用于治疗再生障碍性贫血。

Use of eltrombopag in aplastic anemia in Europe.

机构信息

Department of Hematology, University Hospital Basel, Petersgraben 4, 4031, Basel, Switzerland.

Hopital St. Louis, Paris, France.

出版信息

Ann Hematol. 2019 Jun;98(6):1341-1350. doi: 10.1007/s00277-019-03652-8. Epub 2019 Mar 26.

DOI:10.1007/s00277-019-03652-8
PMID:30915499
Abstract

Eltrombopag (ELT), an oral thrombopoietin receptor agonist, has recently emerged as a promising new drug for the treatment of aplastic anemia (AA). How ELT is used outside of clinical trials in the real-world setting and results of this treatment are not known. We conducted therefore a retrospective survey on the use of ELT in AA among EBMT member centers. We analyzed the 134 patients reported in our survey together with 46 patients recently published by Lengline et al. The median follow-up from start of ELT treatment was 15.3 months, with 85.6% patients alive at last follow-up. Importantly, only 28.9% of our patients received ELT according to the FDA/EMA label as monotherapy in the relapsed/refractory setting, whereas 16.7% received ELT upfront. The overall response rate in our cohort was 62%, very similar to the results of the pivotal ELT trial. In multivariate analysis, combination therapy with ELT/cyclosporine/ATG and response to previous therapy were associated with response. Overall survival was favorable with a 1-year survival from ELT start of 87.4%. We identified age, AA severity before ELT start and response to ELT as variables significantly associated with OS. Two patients transformed to MDS; other adverse events were mostly benign. In sum, ELT is used widely in Europe to treat AA patients, mostly in the relapsed/refractory setting. Response to ELT is similar to the clinical trial data across different age groups, treatment lines, and treatment combinations and results in favorable survival.

摘要

艾曲波帕(ELT),一种口服的血小板生成素受体激动剂,最近已成为治疗再生障碍性贫血(AA)的一种很有前途的新药。在临床试验之外,ELT 在真实世界环境中的使用情况以及这种治疗的结果尚不清楚。因此,我们对 EBMT 成员中心使用 ELT 治疗 AA 进行了回顾性调查。我们分析了我们调查中报告的 134 例患者,以及 Lengline 等人最近发表的 46 例患者。从开始 ELT 治疗到随访的中位数为 15.3 个月,最后一次随访时 85.6%的患者存活。重要的是,只有 28.9%的患者按照 FDA/EMA 标签在复发/难治性情况下接受 ELT 作为单药治疗,而 16.7%的患者接受 ELT 作为一线治疗。我们队列的总体缓解率为 62%,与关键的 ELT 试验结果非常相似。多变量分析显示,ELT/环孢素/ATG 联合治疗和对先前治疗的反应与反应相关。总体生存率良好,从开始 ELT 治疗到 1 年的生存率为 87.4%。我们确定年龄、ELT 开始前的 AA 严重程度和对 ELT 的反应是与 OS 显著相关的变量。两名患者转化为 MDS;其他不良事件大多是良性的。总之,ELT 在欧洲被广泛用于治疗 AA 患者,主要是在复发/难治性情况下。ELT 的反应与临床试验数据在不同年龄组、治疗线和治疗组合中相似,结果是生存率良好。

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Use of eltrombopag in aplastic anemia in Europe.在欧洲,艾曲波帕被用于治疗再生障碍性贫血。
Ann Hematol. 2019 Jun;98(6):1341-1350. doi: 10.1007/s00277-019-03652-8. Epub 2019 Mar 26.
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