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聚乙二醇化干扰素α-2b在真性红细胞增多症和原发性血小板增多症患者中的真实世界研究

Pegylated Interferon Alpha-2b in Patients With Polycythemia Vera and Essential Thrombocythemia in the Real World.

作者信息

Sun Yingxin, Cai Yifeng, Cen Jiannong, Zhu Mingqing, Pan Jinlan, Wang Qian, Wu Depei, Chen Suning

机构信息

Department of Hematology, First Affiliated Hospital of Soochow University, Soochow University, Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases, Suzhou, China.

Department of Thrombosis and Hemostasis, Key Laboratory of Thrombosis and Hemostasis of Ministry of Health, Suzhou, China.

出版信息

Front Oncol. 2021 Dec 21;11:797825. doi: 10.3389/fonc.2021.797825. eCollection 2021.

Abstract

Several clinical trials have shown promising efficacy of pegylated interferon (Peg-IFN) in the first- and second-line polycythemia vera (PV) and essential thrombocythemia (ET). However, the efficacy and safety of Peg-IFN in the real world have rarely been reported. Hence, we conducted a prospective, single-center, single-arm, open exploratory study, which aimed to explore the hematologic response, molecular response, safety, and tolerability of patients with PV and ET treated with Peg-IFN in the real world. This study included newly diagnosed or previously treated patients with PV and ET, aged 18 years or older, admitted to the Department of Hematology of the First Affiliated Hospital of Soochow University from November 2017 to October 2019. The results revealed that complete hematological response (CHR) was achieved in 66.7% of patients with PV and 76.2% of patients with ET, and the molecular response was obtained in 38.5% of patients with PV and 50% of patients with ET after 48 weeks of Peg-IFN treatment. Peg-IFN is safe, effective and well tolerated in most patients. In the entire cohort, 4 patients (9.1%) discontinued treatment due to drug-related toxicity. In conclusion, Peg-IFN is a promising strategy in myeloproliferative neoplasms (MPNs), and Peg-IFN alone or in combination with other drugs should be further explored to reduce treatment-related toxicity and improve tolerability.

摘要

多项临床试验表明,聚乙二醇化干扰素(Peg-IFN)在真性红细胞增多症(PV)和原发性血小板增多症(ET)的一线和二线治疗中疗效显著。然而,Peg-IFN在现实世界中的疗效和安全性鲜有报道。因此,我们开展了一项前瞻性、单中心、单臂、开放性探索性研究,旨在探讨PV和ET患者在现实世界中接受Peg-IFN治疗后的血液学反应、分子反应、安全性和耐受性。本研究纳入了2017年11月至2019年10月期间在苏州大学附属第一医院血液科住院的18岁及以上新诊断或既往接受过治疗的PV和ET患者。结果显示,Peg-IFN治疗48周后,66.7%的PV患者和76.2%的ET患者实现了完全血液学缓解(CHR),38.5%的PV患者和50%的ET患者获得了分子反应。Peg-IFN在大多数患者中安全、有效且耐受性良好。在整个队列中,4例患者(9.1%)因药物相关毒性而停药。总之,Peg-IFN在骨髓增殖性肿瘤(MPN)中是一种有前景的治疗策略,应进一步探索Peg-IFN单药或与其他药物联合使用,以降低治疗相关毒性并提高耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af8e/8724125/7758e4917e89/fonc-11-797825-g001.jpg

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