Hematology, Diabetes, and Endocrinology, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
Department of Hematology, Juntendo University School of Medicine, Tokyo, Japan.
Int J Hematol. 2024 Sep;120(3):314-324. doi: 10.1007/s12185-024-03822-z. Epub 2024 Aug 7.
Momelotinib, an oral Janus kinase (JAK) 1/2 and activin A receptor type 1 inhibitor, improved symptoms, splenomegaly, and anemia in patients with myelofibrosis (MF). This sub-analysis of SIMPLIFY-1 evaluated the efficacy and safety of momelotinib versus ruxolitinib in Japanese patients with JAK inhibitor (JAKi)-naïve MF. Patients were randomized 1:1 to receive momelotinib 200 mg once daily or ruxolitinib 20 mg twice daily (or modified based on label) for 24 weeks, after which patients could receive open-label momelotinib. The primary endpoint was splenic response rate (SRR; ≥ 35% reduction in spleen volume) at 24 weeks; main secondary endpoints were total symptom score (TSS) response (≥ 50% reduction) and transfusion independence (TI) rates. Fifteen Japanese patients (momelotinib, n = 6; ruxolitinib, n = 9) were enrolled; all completed treatment. At Week 24, SRR was 50.0% with momelotinib and 44.4% with ruxolitinib. TSS response rates were 33.3% and 0%, and TI rates were 83.3% and 44.4%. Any-grade treatment-related adverse event (TRAE) rates were 83.3% with momelotinib and 88.9% with ruxolitinib. Grade 3/4 TRAE rates were 0% and 55.6%, with specific events being anemia (55.6%) and vertigo (11.1%) with ruxolitinib. Momelotinib was well tolerated, improved spleen and symptom responses, and reduced transfusion requirements in Japanese patients with JAKi-naïve MF.
莫米松,一种口服 Janus 激酶(JAK)1/2 和激活素 A 受体 1 抑制剂,可改善骨髓纤维化(MF)患者的症状、脾肿大和贫血。SIMPLIFY-1 的这项亚分析评估了 momelotinib 与 ruxolitinib 在日本 JAK 抑制剂(JAKi)初治 MF 患者中的疗效和安全性。患者按 1:1 随机接受莫米松 200mg 每日一次或 ruxolitinib 20mg 每日两次(或根据标签调整)治疗 24 周,之后患者可接受开放标签莫米松治疗。主要终点是 24 周时的脾脏反应率(SRR;脾脏体积减少≥35%);主要次要终点是总症状评分(TSS)反应(减少≥50%)和输血独立性(TI)率。15 名日本患者(莫米松组,n=6;鲁索利替尼组,n=9)入组,均完成治疗。第 24 周时,莫米松组的 SRR 为 50.0%,鲁索利替尼组为 44.4%。TSS 反应率分别为 33.3%和 0%,TI 率分别为 83.3%和 44.4%。莫米松组的任何级别治疗相关不良事件(TRAE)发生率为 83.3%,鲁索利替尼组为 88.9%。3/4 级 TRAE 发生率分别为 0%和 55.6%,具体事件为贫血(55.6%)和眩晕(11.1%)。莫米松在日本 JAKi 初治 MF 患者中耐受性良好,可改善脾脏和症状反应,减少输血需求。