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人源化抗CD25单克隆抗体在单倍体相合异基因造血干细胞移植中替代甲氨蝶呤用于预防急性移植物抗宿主病。

Humanized anti-CD25 monoclonal antibody replaces methotrexate as acute graft-versus-host disease prophylaxis in haploidentical allogeneic haematopoietic stem cell transplantation.

作者信息

Zhang Ao, Huang Zhenli, Zhang Ran, Wei Ruowen, Jiang Shan, Chen Hongru, Cao Xiena, Shi Wei, Xia Linghui, Hu Yu

机构信息

Institute of Hematology, Union Hospital, Tongji Medicine College, Huazhong University of Science and Technology, Wuhan, China.

Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Br J Haematol. 2025 Feb;206(2):615-627. doi: 10.1111/bjh.19958. Epub 2024 Dec 22.

Abstract

Acute graft-versus-host disease (aGVHD) significantly affects quality of life and outcomes in patients post-haploidentical haematopoietic stem cell transplantation (haplo-HSCT). Methotrexate (MTX) is commonly used to prevent aGVHD but can lead to complications like delayed haematological recovery and oral mucositis (OM). This study investigates the efficacy of anti-CD25 monoclonal antibody (mAb) as a potential MTX alternative. Participants were divided into two cohorts: a single-dose group (25 mg/day anti-CD25 mAb with MTX) and a double-dose group (50 mg/day anti-CD25 mAb without MTX). The primary end-point was the cumulative incidence (CI) of severe aGVHD by day 100. The double-dose cohort demonstrated a significantly lower CI of total aGVHD (23.53% vs. 42.11%, p = 0.009) and grade 3-4 aGVHD (7.35% vs. 18.42%, p = 0.047). After inverse probability of treatment weighting adjustment, the adjusted HR of double-dose compared with single-dose cohort for total aGVHD was 0.47 (95% CI 0.26-0.86; p = 0.015), 0.42(95% CI 0.15-1.22; p = 0.110) for grade III-IV aGVHD, 0.45 (95% CI 0.26-0.77; p = 0.004) for total cGVHD and 0.36 (95% CI 0.18-0.72; p = 0.004) for the moderate to severe cGVHD. Additionally, this double-dose regimen significantly reduced the incidence of oral mucositis and demonstrated lower rates of infections and haemorrhagic cystitis. These findings suggest that a double-dose anti-CD25 mAb regimen without MTX is a promising strategy for aGVHD prophylaxis in haplo-HSCT (ChiCTR2200060184).

摘要

急性移植物抗宿主病(aGVHD)显著影响单倍体造血干细胞移植(haplo-HSCT)后患者的生活质量和预后。甲氨蝶呤(MTX)常用于预防aGVHD,但可能导致诸如血液学恢复延迟和口腔黏膜炎(OM)等并发症。本研究调查抗CD25单克隆抗体(mAb)作为MTX潜在替代药物的疗效。参与者被分为两个队列:单剂量组(每天25毫克抗CD25 mAb联合MTX)和双剂量组(每天50毫克抗CD25 mAb不联合MTX)。主要终点是第100天时重度aGVHD的累积发生率(CI)。双剂量队列显示总的aGVHD的CI显著更低(23.53%对42.11%,p = 0.009)以及3-4级aGVHD的CI显著更低(7.35%对18.42%,p = 0.047)。在进行治疗权重逆概率调整后,双剂量组与单剂量组相比,总的aGVHD的调整后风险比为0.47(95%置信区间0.26 - 0.86;p = 0.015),III - IV级aGVHD为0.42(95%置信区间0.15 - 1.22;p = 0.110),总的慢性移植物抗宿主病(cGVHD)为0.45(95%置信区间0.26 - 0.77;p = 0.004),中度至重度cGVHD为0.36(95%置信区间0.18 - 0.72;p = 0.004)。此外,这种双剂量方案显著降低了口腔黏膜炎的发生率,并显示出感染和出血性膀胱炎的发生率更低。这些发现表明,不使用MTX的双剂量抗CD25 mAb方案是haplo-HSCT中预防aGVHD的一种有前景的策略(中国临床试验注册中心注册号:ChiCTR2200060184)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8a1/11829143/06aef5af986e/BJH-206-615-g001.jpg

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