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

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. METHO...

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Autores principales: Mei, Heng, Liu, Xiaofan, Li, Yan, Zhou, Hu, Feng, Ying, Gao, Guangxun, Cheng, Peng, Huang, Ruibin, Yang, Linhua, Hu, Jianda, Hou, Ming, Yao, Yazhou, Liu, Li, Wang, Yi, Wu, Depei, Zhang, Liansheng, Zheng, Changcheng, Shen, Xuliang, Hu, Qi, Liu, Jing, Jin, Jie, Luo, Jianmin, Zeng, Yun, Gao, Sujun, Zhang, Xiaohui, Zhou, Xin, Shi, Qingzhi, Xia, Ruixiang, Xie, Xiaobao, Jiang, Zhongxing, Gao, Li, Bai, Yuansong, Xiong, Junye, Li, Runzi, Zou, Jianjun, Niu, Ting, Yang, Renchi, Hu, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905908/
https://www.ncbi.nlm.nih.gov/pubmed/33632264
http://dx.doi.org/10.1186/s13045-021-01047-9
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author Mei, Heng
Liu, Xiaofan
Li, Yan
Zhou, Hu
Feng, Ying
Gao, Guangxun
Cheng, Peng
Huang, Ruibin
Yang, Linhua
Hu, Jianda
Hou, Ming
Yao, Yazhou
Liu, Li
Wang, Yi
Wu, Depei
Zhang, Liansheng
Zheng, Changcheng
Shen, Xuliang
Hu, Qi
Liu, Jing
Jin, Jie
Luo, Jianmin
Zeng, Yun
Gao, Sujun
Zhang, Xiaohui
Zhou, Xin
Shi, Qingzhi
Xia, Ruixiang
Xie, Xiaobao
Jiang, Zhongxing
Gao, Li
Bai, Yuansong
Li, Yan
Xiong, Junye
Li, Runzi
Zou, Jianjun
Niu, Ting
Yang, Renchi
Hu, Yu
author_facet Mei, Heng
Liu, Xiaofan
Li, Yan
Zhou, Hu
Feng, Ying
Gao, Guangxun
Cheng, Peng
Huang, Ruibin
Yang, Linhua
Hu, Jianda
Hou, Ming
Yao, Yazhou
Liu, Li
Wang, Yi
Wu, Depei
Zhang, Liansheng
Zheng, Changcheng
Shen, Xuliang
Hu, Qi
Liu, Jing
Jin, Jie
Luo, Jianmin
Zeng, Yun
Gao, Sujun
Zhang, Xiaohui
Zhou, Xin
Shi, Qingzhi
Xia, Ruixiang
Xie, Xiaobao
Jiang, Zhongxing
Gao, Li
Bai, Yuansong
Li, Yan
Xiong, Junye
Li, Runzi
Zou, Jianjun
Niu, Ting
Yang, Renchi
Hu, Yu
author_sort Mei, Heng
collection PubMed
description 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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spelling pubmed-79059082021-02-26 A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia Mei, Heng Liu, Xiaofan Li, Yan Zhou, Hu Feng, Ying Gao, Guangxun Cheng, Peng Huang, Ruibin Yang, Linhua Hu, Jianda Hou, Ming Yao, Yazhou Liu, Li Wang, Yi Wu, Depei Zhang, Liansheng Zheng, Changcheng Shen, Xuliang Hu, Qi Liu, Jing Jin, Jie Luo, Jianmin Zeng, Yun Gao, Sujun Zhang, Xiaohui Zhou, Xin Shi, Qingzhi Xia, Ruixiang Xie, Xiaobao Jiang, Zhongxing Gao, Li Bai, Yuansong Li, Yan Xiong, Junye Li, Runzi Zou, Jianjun Niu, Ting Yang, Renchi Hu, Yu J Hematol Oncol Research 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. BioMed Central 2021-02-25 /pmc/articles/PMC7905908/ /pubmed/33632264 http://dx.doi.org/10.1186/s13045-021-01047-9 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mei, Heng
Liu, Xiaofan
Li, Yan
Zhou, Hu
Feng, Ying
Gao, Guangxun
Cheng, Peng
Huang, Ruibin
Yang, Linhua
Hu, Jianda
Hou, Ming
Yao, Yazhou
Liu, Li
Wang, Yi
Wu, Depei
Zhang, Liansheng
Zheng, Changcheng
Shen, Xuliang
Hu, Qi
Liu, Jing
Jin, Jie
Luo, Jianmin
Zeng, Yun
Gao, Sujun
Zhang, Xiaohui
Zhou, Xin
Shi, Qingzhi
Xia, Ruixiang
Xie, Xiaobao
Jiang, Zhongxing
Gao, Li
Bai, Yuansong
Li, Yan
Xiong, Junye
Li, Runzi
Zou, Jianjun
Niu, Ting
Yang, Renchi
Hu, Yu
A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
title A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
title_full A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
title_fullStr A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
title_full_unstemmed A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
title_short A multicenter, randomized phase III trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
title_sort multicenter, randomized phase iii trial of hetrombopag: a novel thrombopoietin receptor agonist for the treatment of immune thrombocytopenia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905908/
https://www.ncbi.nlm.nih.gov/pubmed/33632264
http://dx.doi.org/10.1186/s13045-021-01047-9
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