Sato Shuku, Tsunoda Shun, Kamata Wataru, Togano Tomiteru, Tamai Yotaro
Division of Hematology, Shonan Kamakura General Hospital.
Tamai Clinic of Internal Medicine.
Rinsho Ketsueki. 2025;66(2):92-99. doi: 10.11406/rinketsu.66.92.
Combination of immunosuppressive therapy (IST) and thrombopoietin receptor agonists has revolutionized the treatment of aplastic anemia. In this study, 18 patients with eltrombopag (EPAG)-refractory and intolerant AA, including 16 with severe AA, were switched from EPAG to romiplostim and continued with romiplostim for at least three months. Of the 18 patients (7 refractory and 11 intolerant to EPAG), 13 (72%) achieved a response, with a therapeutic response in at least one lineage within three months, and nine patients (50%) showed a trilineage response. All three patients who started romiplostim over three years after diagnosis failed to respond to romiplostim. In three of the four patients with adequate response to romiplostim, interruption of romiplostim resulted in relapsed thrombocytopenia, and early resumption of romiplostim resulted in recovered blood counts. These results suggest that romiplostim may achieve a response in IST+EPAG refractory/intolerant SAA.
免疫抑制疗法(IST)与血小板生成素受体激动剂联合使用彻底改变了再生障碍性贫血的治疗方法。在本研究中,18例对艾曲泊帕(EPAG)难治或不耐受的再生障碍性贫血患者,包括16例重型再生障碍性贫血患者,从EPAG转换为罗米司亭,并继续使用罗米司亭至少三个月。在这18例患者中(7例对EPAG难治,11例对EPAG不耐受),13例(72%)获得缓解,即在三个月内至少有一个谱系出现治疗反应,9例患者(50%)表现为三系反应。所有在诊断三年后开始使用罗米司亭的3例患者对罗米司亭均无反应。在对罗米司亭有充分反应的4例患者中的3例,中断罗米司亭导致血小板减少复发,而早期恢复使用罗米司亭则使血细胞计数恢复。这些结果表明,罗米司亭可能对IST+EPAG难治/不耐受的重型再生障碍性贫血有效。