Correlation between a 2-week change in platelet count and clinical outcomes after the initiation of ravulizumab treatment in adult patients with atypical hemolytic uremic syndrome: post-hoc analysis of the phase III trial.

IF 2.6 4区 医学 Q2 HEMATOLOGY Thrombosis Journal Pub Date : 2024-10-28 DOI:10.1186/s12959-024-00652-1
Masanori Matsumoto, Akihiko Shimono, Jun Yokosawa, Keiichiro Hirose, Edward Wang, Shoichi Maruyama
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引用次数: 0

Abstract

Background: Atypical hemolytic uremic syndrome (aHUS) is a rare disease with poor outcomes when untreated, in which ravulizumab or eculizumab are the standard of care where available. It has been proposed to regularly monitor platelet counts as an early response to ravulizumab or eculizumab. This study aimed to investigate the association between the early response to ravulizumab treatment and renal outcomes through 26 weeks in complement inhibitor-naïve adults with aHUS.

Methods: Adult patients with aHUS enrolled in the ALXN1210-aHUS-311 phase III study of ravulizumab were divided into two groups according to the achievement of complete thrombotic microangiopathy (TMA) response, i.e., platelet count and lactate dehydrogenase (LDH) normalization and ≥ 25% improvement in serum creatinine (sCr) from baseline, by 26 weeks and baseline characteristics were compared. Changes in hematologic parameters, platelet count and LDH, were compared between the two groups. Finally, we examined whether early hematologic improvement was associated with renal recovery (dialysis discontinuation or ≥ 25% improvement in sCr from baseline) through 26 weeks.

Results: Of 56 ravulizumab-treated patients, 30 achieved complete TMA response for 26 weeks, and 26 did not. Patients with complete TMA response showed rapid improvements in platelet counts. In patients without complete TMA response, delayed normalization of platelet counts was observed. By day 15, 93.3% (28/30) of patients with complete TMA response at 26 weeks and 26.9% (7/26) of patients without complete TMA response achieved platelet normalization. At 26 weeks, 62.5% (35/56) achieved renal recovery; however, 37.5% (21/56) did not. In patients with renal recovery, 85.7% (30/35) of patients had platelet count normalization by day 15; in patients without renal recovery, 23.8% (5/21) of patients had platelet count normalization (P < 0.0001). Receiver operator characteristic curve analysis showed a moderate association between platelet counts on day 8/15 and renal recovery within 26 weeks (day 8: area under the curve [AUC] = 0.7985; day 15: AUC = 0.8406).

Conclusions: Platelet count normalization occurred in 62.5% (35/56) by day 15 after ravulizumab initiation and was associated with renal recovery through 26 weeks in complement inhibitor-naïve adults with aHUS.

Trial registration: This study was performed as a post-hoc analysis of the ALXN1210-aHUS-311 phase III clinical trial (NCT02949128, registered October 25, 2016).

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非典型溶血性尿毒症综合征成年患者开始接受雷珠单抗治疗后 2 周血小板计数变化与临床结果之间的相关性:III 期试验的事后分析。
背景:非典型溶血性尿毒症综合征(aHUS)是一种罕见疾病,如不及时治疗,预后很差。有人建议定期监测血小板计数,作为对雷珠单抗或依库珠单抗的早期反应。本研究旨在调查补体抑制剂无效的成人 aHUS 患者对雷珠单抗治疗的早期反应与持续 26 周的肾脏预后之间的关联:参加ALXN1210-aHUS-311雷珠单抗III期研究的成人aHUS患者根据26周前血栓性微血管病(TMA)完全应答(即血小板计数和乳酸脱氢酶(LDH)正常化且血清肌酐(sCr)较基线改善≥25%)的实现情况分为两组,并比较基线特征。比较了两组患者血液学参数、血小板计数和 LDH 的变化。最后,我们研究了早期血液学指标的改善是否与持续 26 周的肾功能恢复(停止透析或 sCr 从基线改善≥ 25%)相关:结果:在 56 名接受雷珠单抗治疗的患者中,30 人在 26 周内实现了完全 TMA 反应,26 人未实现。完全TMA反应患者的血小板计数迅速改善。在没有完全TMA反应的患者中,观察到血小板计数延迟恢复正常。到第 15 天,93.3%(28/30)的完全 TMA 反应患者(26 周)和 26.9%(7/26)的未完全 TMA 反应患者(26 周)实现了血小板正常化。在 26 周时,62.5%(35/56)的患者实现了肾功能恢复;然而,37.5%(21/56)的患者未实现肾功能恢复。在肾功能恢复的患者中,85.7%(30/35)的患者在第 15 天时血小板计数恢复正常;在肾功能未恢复的患者中,23.8%(5/21)的患者血小板计数恢复正常(P 结论:在肾功能恢复的患者中,血小板计数恢复正常的患者占总人数的比例较高,而在肾功能未恢复的患者中,血小板计数恢复正常的患者占总人数的比例较低:在补体抑制剂无效的成人 aHUS 患者中,62.5%(35/56)的患者在开始使用雷武珠单抗后第 15 天血小板计数恢复正常,并在 26 周内实现肾功能恢复:本研究是作为ALXN1210-aHUS-311 III期临床试验(NCT02949128,2016年10月25日注册)的事后分析进行的。
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来源期刊
Thrombosis Journal
Thrombosis Journal Medicine-Hematology
CiteScore
3.80
自引率
3.20%
发文量
69
审稿时长
16 weeks
期刊介绍: Thrombosis Journal is an open-access journal that publishes original articles on aspects of clinical and basic research, new methodology, case reports and reviews in the areas of thrombosis. Topics of particular interest include the diagnosis of arterial and venous thrombosis, new antithrombotic treatments, new developments in the understanding, diagnosis and treatments of atherosclerotic vessel disease, relations between haemostasis and vascular disease, hypertension, diabetes, immunology and obesity.
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