ECLIPSE-PV: A Randomized, Multicenter Study to Assess Efficacy, Safety, and Tolerability of Two Dosing Regimens of Ropeginterferon Alfa-2b-Njft in Polycythemia Vera.

IF 1.1 4区 医学 Q3 HEMATOLOGY
John Mascarenhas, Prithviraj Bose, Christopher Hillis, Abdulraheem Yacoub, Firas El Chaer, Dawn Maze, Ghaith Abu-Zeinah, Albert Qin, Victor Priego, Tsewang Tashi, Sonia Cerquozzi, Sunil Babu, Lynda Foltz, Swati Goel, Rupali R Bhave, Stephanie Lee, Stephen T Oh, Brandi Reeves, Christopher Benton, Luke Fletcher, Shireen Sirhan, Hana Safah, Hayman Salib, Pierre J A Villeneuve, Oleh Zagrijtschuk, Henry Castro, Lucia Masarova
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引用次数: 0

Abstract

Introduction: Ropeginterferon alfa-2b-njft (ropeg) was approved and recommended as a preferred cytoreductive treatment for polycythemia vera (PV). The approved regimen requires an initial dose of 100 μg or 50 μg if transitioning from hydroxyurea (HU) and up-titrations of 50 μg every 2 weeks to 500 μg maximumly. The time to achieve the plateau dose takes approximately 20 weeks. This study compares the approved regimen with a higher initial dose and accelerated dose titration (HIDAT) regimen.

Methods: ECLIPSE-PV is a randomized, open-label, multicenter trial in patients with PV in the USA and Canada. Patients received ropeg either per the approved dosing schema or HIDAT regimen, i.e., 250 μg on day 0, 350 μg at week 2, and 500 μg from week 4 thereafter if tolerable. The primary endpoint is complete hematologic response (CHR) rate at week 24. CHR is defined as hematocrit <45%, white blood cells <10 × 109/L, platelets ≤400 × 109/L without phlebotomy in the previous 12 weeks. Secondary endpoints include molecular response, safety, tolerability, and quality of life.

Conclusion: A total of 111 patients were randomized and the last patient was enrolled on June 21, 2024. As of November 12, 2024, the discontinuation rate was 14.4%, and 16 patients (14.4%) completed the study. The study is expected to be completed in the summer of 2025. This is the first prospective trial comparing two dosing regimens of ropeg. The results will inform the optimal treatment strategy for patients with PV.

ECLIPSE-PV:一项随机、多中心研究,评估两种给药方案对真性红细胞增多症的有效性、安全性和耐受性。
ropeg干扰素alfa-2b-njft (ropeg)被批准并推荐为真性红细胞增多症(PV)的首选细胞减少治疗药物。批准的方案要求初始剂量为100 μg,如果从羟基脲(HU)过渡到50 μg,每两周增加50 μg,最多增加500 μg。达到平台剂量的时间大约需要20周。本研究将批准的方案与较高初始剂量和加速剂量滴定(HIDAT)方案进行比较。方法与结论:ECLIPSE-PV是一项随机、开放标签、多中心试验,在美国和加拿大的PV患者中进行。患者根据批准的给药方案或HIDAT方案接受ropeg治疗,即第0天250 μg,第2周350 μg,此后第4周500 μg(如果耐受)。主要终点是第24周的完全血液学反应(CHR)率。CHR定义为红细胞压积
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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