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Jakinib 治疗初治骨髓纤维化患者的安全性和疗效:一项 II 期试验结果。

Safety and efficacy of jaktinib in the treatment of Janus kinase inhibitor-naïve patients with myelofibrosis: Results of a phase II trial.

机构信息

Department of Hematology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, P.R. China.

Zhejiang Provincial Key Laboratory of Hematopoietic Malignancy, Zhejiang University, Hangzhou, P.R. China.

出版信息

Am J Hematol. 2022 Dec;97(12):1510-1519. doi: 10.1002/ajh.26709. Epub 2022 Oct 4.

Abstract

Myelofibrosis (MF) is associated with several constitutional symptoms. Currently, there are few therapeutic options for MF. Jaktinib, a novel, small-molecule inhibitor of JAK, is currently being studied for its potential to treat MF. This phase 2 trial investigated efficacy and safety of jaktinib in the treatment of MF patients. The primary end point was the proportion of patients with ≥35% reduction in spleen volume (SVR35, proportion of patients with ≥35% reduction in spleen volume) at week 24. The secondary end points included improvement of anemia, rates of symptom response, and safety profile. Between January 8, 2019 and August 29, 2020, 118 patients were recruited and treated with either jaktinib 100 mg BID or 200 mg QD. At week 24, 54.8% (34/62) of patients in the 100 mg BID group and 31.3% (15/48) in the 200 mg QD group achieved SVR35 (p = .0199). Jaktinib treatment increased hemoglobin level to ≥20 g/L in 35.6% (21/59) of patients with hemoglobin ≤100 g/L at baseline. The proportion of patients who achieved a ≥50% improvement in total symptom score at week 24 was 69.6% (39/56) in the BID group and 57.5% (23/40) in the QD group. The most common ≥ grade 3 hematological treatment-emergent adverse events (TEAEs; ≥ 10%) were anemia (100 mg BID: 24.2%, 200 mg QD: 28.8%), thrombocytopenia (16.7%, 11.5%), and neutropenia (3.0%, 11.5%). All non-hematological TEAEs were mild. These results indicate that jaktinib can shrink the spleen, improve anemia, and other clinical symptoms with good tolerability.

摘要

骨髓纤维化(MF)与多种全身症状相关。目前,MF 的治疗选择有限。Jak 激酶小分子抑制剂 Jaktinib 目前正在研究用于治疗 MF 的潜力。这项 2 期临床试验研究了 Jaktinib 治疗 MF 患者的疗效和安全性。主要终点是 24 周时脾脏体积减少≥35%的患者比例(SVR35,脾脏体积减少≥35%的患者比例)。次要终点包括贫血改善、症状缓解率和安全性特征。2019 年 1 月 8 日至 2020 年 8 月 29 日,共招募了 118 名患者,分别接受 Jaktinib 100mg BID 或 200mg QD 治疗。24 周时,100mg BID 组 54.8%(34/62)和 200mg QD 组 31.3%(15/48)的患者达到 SVR35(p=0.0199)。Jaktinib 治疗使基线时血红蛋白≤100g/L 的 35.6%(21/59)患者的血红蛋白水平升高至≥20g/L。24 周时,总症状评分改善≥50%的患者比例在 BID 组为 69.6%(39/56),QD 组为 57.5%(23/40)。最常见的≥3 级血液学治疗相关不良事件(TEAEs;≥10%)是贫血(100mg BID:24.2%,200mg QD:28.8%)、血小板减少症(16.7%,11.5%)和中性粒细胞减少症(3.0%,11.5%)。所有非血液学 TEAEs 均为轻度。这些结果表明 Jaktinib 可缩小脾脏,改善贫血和其他临床症状,且具有良好的耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b27/10092883/0157d8cd2b4b/AJH-97-1510-g002.jpg

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