Department of Hematology, NTT Medical Center Tokyo, 5-9-22 Higashigotanda, Shinagawa-ku, Tokyo, 141-8625, Japan.
Int J Hematol. 2020 Dec;112(6):787-794. doi: 10.1007/s12185-020-02971-1. Epub 2020 Sep 2.
Eltrombopag (EPAG) and romiplostim (ROM), thrombopoietin receptor-agonists with demonstrated efficacy against aplastic anemia (AA) in prospective controlled studies, were authorized in Japan for use in adults with aplastic anemia in 2017 and 2019, respectively. So far, no data are available on the potential contribution of switching from ROM to EPAG or vice versa in terms of efficacy or tolerance. Efficacies and tolerance profiles of ten patients, who failed to respond to the maximum dose of EPAG and then switched to ROM, were evaluated. All ten patients received a maximum dose of ROM (20 μg/kg/week). At a median follow-up of twelve months, seven of ten patients (70%) had achieved either neutrophil, erythroid, or platelet response, including one complete response. No patients showed platelet count fluctuations that were reported during ROM treatment for immune thrombocytopenia. In univariate analysis of the relationship between efficacy and demographics, the response had a correlation with neither factors. None of the patients stopped the ROM treatment because of adverse events. Although a larger number of patients and a longer follow-up period are needed to confirm our findings, our results show the efficacy of ROM in patients with EPAG-refractory AA.
依洛尤单抗(EPAG)和罗米司亭(ROM)是两种已被证明在针对再生障碍性贫血(AA)的前瞻性对照研究中有效的血小板生成素受体激动剂,分别于 2017 年和 2019 年在日本被批准用于治疗成人再生障碍性贫血。迄今为止,尚无关于 ROM 换用 EPAG 或 EPAG 换用 ROM 对疗效或耐受性的潜在影响的相关数据。本研究评估了 10 名 EPAG 最大剂量治疗无效后换用 ROM 的患者的疗效和耐受性。所有 10 名患者均接受了最大剂量的 ROM(20μg/kg/周)治疗。中位随访 12 个月时,7 名患者(70%)获得了中性粒细胞、红细胞或血小板反应,包括 1 名完全缓解患者。无患者出现报告的 ROM 治疗免疫性血小板减少症期间的血小板计数波动。在对疗效与人口统计学因素的单因素分析中,反应与两者均无相关性。无患者因不良事件停止 ROM 治疗。尽管需要更多的患者和更长的随访时间来证实我们的发现,但我们的结果表明 ROM 对 EPAG 难治性 AA 患者有效。