Managing transient immune complex reactions in patients with paroxysmal nocturnal hemoglobinuria: clinical observations from the COMMODORE 1 and 2 studies.

IF 3.1 3区 医学 Q2 HEMATOLOGY
Therapeutic Advances in Hematology Pub Date : 2025-09-17 eCollection Date: 2025-01-01 DOI:10.1177/20406207251359246
Austin G Kulasekararaj, Jun-Ichi Nishimura, Alexander Röth, Leigh Beveridge, Simon Buatois, Muriel Buri, Nicolo Compagno, Yves Luder, Sasha Sreckovic, Phillip Scheinberg
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引用次数: 0

Abstract

Background: Crovalimab is a novel C5 inhibitor that enables rapid and sustained C5 inhibition with every 4-week subcutaneous maintenance dosing, with the possibility for self-administration. When switching from another C5 inhibitor (binds to a different epitope than crovalimab) to crovalimab and vice versa, transient immune complexes will form and may cause transient immune complex reactions (TICRs).

Objectives: To assess TICR occurrence, manifestation, and management in patients with paroxysmal nocturnal hemoglobinuria (PNH) who switched from another C5 inhibitor to crovalimab.

Design: COMMODORE 1 and 2 randomized C5 inhibitor-experienced and -naïve patients, respectively, to receive crovalimab or eculizumab. The COMMODORE 1 nonrandomized, descriptive cohort included patients who previously received ravulizumab or approved or higher-than-approved doses of eculizumab.

Methods: Pooled data of patients who switched from eculizumab or ravulizumab to crovalimab were evaluated for TICR incidence and severity. TICR treatments and TICR durations were assessed by severity.

Results: This descriptive analysis included 201 patients who switched from eculizumab (n = 174) or ravulizumab (n = 27) to crovalimab. Baseline characteristics were generally balanced between patients with and without a TICR. Thirty-nine of 201 patients (19%) experienced TICRs (11% Grades 1-2; 8% Grade 3; no Grades 4-5). Median time to onset and median TICR duration were 1.6 (range, 0.7-4.4) and 1.7 weeks (range, 0.4-34.1), respectively. The most common symptoms were arthralgia (45%), rash (34%), and pyrexia (21%), with no evidence of renal manifestations. Oral corticosteroids were the most common TICR treatment. Grade 3 TICRs were treated with higher oral corticosteroid dose but did not take longer to resolve than Grades 1-2 TICRs.

Conclusion: Pooled COMMODORE 1 and 2 data show that TICRs from switching between C5 inhibitors were generally mild to moderate and resolved with appropriate treatment. These results further confirm that crovalimab is well tolerated in patients with PNH.

Trial registration: NCT04432584; NCT04434092.

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处理阵发性夜间血红蛋白尿患者的短暂免疫复合物反应:来自COMMODORE 1和2研究的临床观察
背景:Crovalimab是一种新型C5抑制剂,每4周皮下维持给药,可实现快速和持续的C5抑制,并有可能自行给药。当从另一种C5抑制剂(结合与crovalimab不同的表位)切换到crovalimab时,反之亦然,会形成短暂的免疫复合物并可能引起短暂的免疫复合物反应(TICRs)。目的:评估发作性夜间血红蛋白尿(PNH)患者从另一种C5抑制剂切换到克罗伐单抗的TICR发生、表现和管理。设计:COMMODORE 1和2分别随机化C5抑制剂经验和-naïve患者接受crovalimab或eculizumab治疗。COMMODORE 1非随机,描述性队列包括先前接受过ravulizumab或批准或高于批准剂量的eculizumab的患者。方法:对从eculizumab或ravulizumab切换到crovalimab的患者的汇总数据进行TICR发生率和严重程度的评估。根据严重程度评估TICR治疗和TICR持续时间。结果:这项描述性分析包括201例从eculizumab (n = 174)或ravulizumab (n = 27)切换到crovalimab的患者。基线特征在有和没有TICR的患者之间通常是平衡的。201例患者中有39例(19%)经历了ticr(1-2级11%,3级8%,4-5级无)。中位发病时间和中位TICR持续时间分别为1.6周(范围0.7-4.4)和1.7周(范围0.4-34.1)。最常见的症状是关节痛(45%)、皮疹(34%)和发热(21%),无肾脏表现。口服皮质类固醇是最常见的TICR治疗方法。3级TICRs采用较高的口服皮质类固醇剂量治疗,但缓解时间并不比1-2级TICRs长。结论:汇总的COMMODORE 1和2数据显示,切换C5抑制剂引起的ticr通常为轻度至中度,并通过适当的治疗得到解决。这些结果进一步证实,克罗伐单抗在PNH患者中耐受性良好。试验注册:NCT04432584;NCT04434092。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
54
审稿时长
7 weeks
期刊介绍: Therapeutic Advances in Hematology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of hematology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in hematology, providing a forum in print and online for publishing the highest quality articles in this area.
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