Lee Jong Wook, Jang Jun Ho, Chiba Shigeru, Yoon Sung-Soo, Oshikawa Gaku, Usuki Kensuke, Mun Yeung-Chul, Kawakita Toshiro, Imada Kazunori, Cheong June-Won, Noshiro Masayoshi, Matsuda Akira, Ozawa Keiya, Mitani Kinuko, Kanda Yoshinobu, Nakao Shinji
Division of Hematology-Oncology, Hanyang University Seoul Hospital, Seoul, Republic of Korea.
Department of Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Br J Haematol. 2025 Aug;207(2):582-590. doi: 10.1111/bjh.20206. Epub 2025 Jul 10.
Romiplostim has been shown to restore multi-lineage haematopoiesis and is effective in patients with aplastic anaemia (AA) refractory to immunosuppressive therapy (IST). This open-label, phase 2/3 study (NCT04095936) recruited adult AA patients in Japan and Korea who had not received prior IST and evaluated the efficacy and safety of romiplostim plus ciclosporin A (CsA). Romiplostim was initiated at 10 μg/kg once weekly through Week 4 and adjusted between 0 and 20 μg/kg from Week 5 onwards. CsA was administered at 5-6 mg/kg/day in two divided doses through Week 26. A total of 24 patients (median [range] age, 52 [19-80] years) were enrolled, and 22 (91.7%) completed the study. Four patients (16.7%) had very severe AA (VSAA), 13 (54.2%) had severe AA (SAA) and seven (29.2%) had transfusion-dependent non-severe AA (NSAA). A haematological response at Week 27 was observed in 10/24 patients (overall response, 41.7%; 95% confidence interval, 22.1%-63.4%). At Week 27, the subgroup overall response rates were 0.0% in VSAA, 46.2% in SAA and 57.1% in NSAA. Nearly 92% of patients experienced at least one treatment-emergent adverse event (TEAE), but no drug-related Grade ≥3 TEAEs were reported. One patient developed myelodysplastic syndromes. Treatment with romiplostim plus CsA was effective and well tolerated in patients with AA who had not previously received IST.
罗米司亭已被证明可恢复多谱系造血,对免疫抑制治疗(IST)难治的再生障碍性贫血(AA)患者有效。这项开放标签的2/3期研究(NCT04095936)在日本和韩国招募了未接受过先前IST的成年AA患者,并评估了罗米司亭加环孢素A(CsA)的疗效和安全性。罗米司亭在第4周前每周一次以10μg/kg起始,从第5周起在0至20μg/kg之间调整。CsA在第26周前以5 - 6mg/kg/天分两次给药。共纳入24例患者(中位[范围]年龄,52[19 - 80]岁),22例(91.7%)完成研究。4例患者(16.7%)患有极重型AA(VSAA),13例(54.2%)患有重型AA(SAA),7例(29.2%)患有输血依赖型非重型AA(NSAA)。24例患者中有10例在第27周出现血液学反应(总体缓解率,41.7%;95%置信区间,22.1% - 63.4%)。在第27周,VSAA亚组的总体缓解率为0.0%,SAA为46.2%,NSAA为57.1%。近92%的患者经历了至少一次治疗中出现的不良事件(TEAE),但未报告与药物相关的≥3级TEAE。1例患者发生骨髓增生异常综合征。罗米司亭加CsA治疗对先前未接受过IST的AA患者有效且耐受性良好。