A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia

医学 埃尔特罗姆博帕格 血小板生成素受体 安慰剂 内科学 临床终点 血小板生成素 优势比 随机对照试验 胃肠病学 血小板 不利影响 置信区间 罗米普洛斯蒂姆 外科 免疫性血小板减少症 病理 替代医学 造血 生物 遗传学 干细胞
作者
Heng Mei,Xiaofan Liu,Yan Li,Hu Zhou,Ying Feng,Guangxun Gao,Cheng Peng,Ruibin Huang,Linhua Yang,Jianda Hu,Ming Hou,Yazhou Yao,Li Liu,Yi Wang,Depei Wu,Liansheng Zhang,Changcheng Zheng,Xu‐Liang Shen,Qi Hu,Jing Liu,Jie Jin,Jianmin Luo,Yun Zeng,Sujun Gao,Xiaohui Zhang,Xin Zhou,Qingzhi Shi,Ruixiang Xia,Xiaobao Xie,Zhongxing Jiang,Li Gao,Yuansong Bai,Yan Li,Junye Xiong,Runzi Li,Jianjun Zou,Ting Niu,Renchi Yang,Yu Hu
出处
期刊:Journal of Hematology & Oncology [Springer Nature]
卷期号:14 (1) 被引量:43
标识
DOI:10.1186/s13045-021-01047-9
摘要

Abstract Background Hetrombopag, a novel thrombopoietin receptor agonist, has been found in phase I studies to increase platelet counts and reduce bleeding risks in adults with immune thrombocytopenia (ITP). This phase III study aimed to evaluate the efficacy and safety of hetrombopag in ITP patients. Methods Patients who had not responded to or had relapsed after previous treatment were treated with an initial dosage of once-daily 2.5 or 5 mg hetrombopag (defined as the HETROM-2.5 or HETROM-5 group) or with matching placebo in a randomized, double-blind, 10-week treatment period. Patients who received placebo and completed 10 weeks of treatment switched to receive eltrombopag, and patients treated with hetrombopag in the double-blind period continued hetrombopag during the following open-label 14-week treatment. The primary endpoint was the proportion of responders (defined as those achieving a platelet count of ≥ 50 × 10 9 /L) after 8 weeks of treatment. Results The primary endpoint was achieved by significantly more patients in the HETROM-2.5 (58.9%; odds ratio [OR] 25.97, 95% confidence interval [CI] 9.83–68.63; p < 0.0001) and HETROM-5 (64.3%; OR 32.81, 95% CI 12.39–86.87; p < 0.0001) group than in the Placebo group (5.9%). Hetrombopag was also superior to placebo in achieving a platelet response and in reducing the bleeding risk and use of rescue therapy throughout 8 weeks of treatment. The durable platelet response to hetrombopag was maintained throughout 24 weeks. The most common adverse events were upper respiratory tract infection (42.2%), urinary tract infection (17.1%), immune thrombocytopenic purpura (17.1%) and hematuria (15%) with 24-week hetrombopag treatment. Conclusions In ITP patients, hetrombopag is efficacious and well tolerated with a manageable safety profile. Trial registration Clinical trials.gov NCT03222843 , registered July 19, 2017, retrospectively registered.
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