Real-world effectiveness of autologous haematopoietic stem cell transplantation for multiple sclerosis in the UK.

IF 7.5 1区 医学 Q1 CLINICAL NEUROLOGY
Paolo Antonio Muraro, Majid Kazmi, Eleonora De Matteis, Gavin Brittain, Alice Mariottini, Richard Nicholas, Eli Silber, Varun Mehra, Ian Gabriel, Olga Ciccarelli, Julia Lee, Rachel Pearce, Maria Pia Sormani, Alessio Signori, Ruth Paul, Ram Malladi, Victoria Potter, John Snowden, Basil Sharrack
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Abstract

Background: Autologous haematopoietic stem cell transplantation (AHSCT) is increasingly used as a one-off disease-modifying therapy for aggressive forms of multiple sclerosis (MS). We report real-world effectiveness of AHSCT for MS in the UK.

Methods: This retrospective open-label study included patients with (pw)MS treated with AHSCT between 2002 and 2023 in 14 UK centres. Outcomes included relapse-free survival (RFS), MRI activity-free survival (MFS), progression-free survival (PFS) and no evidence of disease activity (NEDA-3). We assessed 6-month confirmed Expanded Disability Status Scale (EDSS) score progression or improvement compared with pre-treatment. Treatment-related mortality (TRM) was defined as death from any cause within 100 days post-autologous graft reinfusion.

Results: 364 pwMS were included (median age 40 years; 58% female). Of these, 271 pwMS had adequate neurological follow-up data: 168 (62%) had relapsing-remitting MS (pwRRMS) and 103 (38%) had progressive MS (pwPMS). Median disease duration from symptom onset was 10 years (IQR 6-14), EDSS 6 (IQR 4.0-6.5) and follow-up from AHSCT 46 months. At 2 and 5 years from AHSCT, RFS was 94.6% and 88.6%; MFS 93.1% and 80.1%; PFS 83.5% and 62.4%; NEDA-3 72.3% and 46.2%. pwRRMS had significantly higher rates of PFS (p=0.007) and NEDA-3 (p=0.001) than pwPMS. RRMS was a predictor of EDSS improvement, whose prevalence was 24.2% at 2 years and 20.4% at 5 years. TRM was 1.4% (n=5/364).

Conclusions: In this cohort with high EDSS at baseline and including pwPMS, AHSCT led to durable remission of inflammatory activity and stabilisation or improvement of neurological disability, particularly in pwRRMS.

在英国,自体造血干细胞移植治疗多发性硬化症的实际效果。
背景:自体造血干细胞移植(AHSCT)越来越多地被用作侵袭性多发性硬化症(MS)的一次性疾病改善疗法。我们报告了AHSCT在英国治疗多发性硬化症的实际效果。方法:这项回顾性开放标签研究纳入了2002年至2023年间在英国14个中心接受AHSCT治疗的(pw)MS患者。结果包括无复发生存期(RFS)、无MRI活动生存期(MFS)、无进展生存期(PFS)和无疾病活动证据(NEDA-3)。与治疗前相比,我们评估了6个月确认的扩展残疾状态量表(EDSS)评分的进展或改善。治疗相关死亡率(TRM)定义为自体移植物再输注后100天内任何原因导致的死亡。结果:纳入364例pwMS患者(中位年龄40岁,58%为女性)。其中,271名pwMS患者有足够的神经学随访数据:168名(62%)患有复发缓解型MS (pwRRMS), 103名(38%)患有进行性MS (pwPMS)。从症状出现开始的中位病程为10年(IQR 6-14), EDSS为6年(IQR 4.0-6.5), AHSCT随访为46个月。AHSCT术后2年和5年,RFS分别为94.6%和88.6%;MFS分别为93.1%和80.1%;PFS分别为83.5%和62.4%;NEDA-3 72.3%和46.2%。pwRRMS的PFS发生率(p=0.007)和NEDA-3发生率(p=0.001)明显高于pwPMS。RRMS是EDSS改善的预测因子,其2年患病率为24.2%,5年患病率为20.4%。TRM为1.4% (n=5/364)。结论:在基线EDSS较高的队列中,包括pwPMS, AHSCT导致炎症活性的持续缓解和神经功能障碍的稳定或改善,特别是pwRRMS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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