CORe, Department of Medicine, University of Melbourne, Parkville, Victoria, Australia
Neuroimmunology Centre, Department of Neurology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
J Neurol Neurosurg Psychiatry. 2024 Jul 15;95(8):775-783. doi: 10.1136/jnnp-2023-332790.
Natalizumab was not shown to modify disability in progressive multiple sclerosis (MS). This matched observational study compared the effectiveness of autologous haematopoietic stem cell transplantation (AHSCT) with natalizumab in progressive MS.
Patients with primary/secondary progressive MS from seven AHSCT MS centres and the MSBase registry, treated with AHSCT or natalizumab, were matched on a propensity score derived from sex, age, Expanded Disability Status Scale (EDSS), number of relapses 12/24 months before baseline, time from MS onset, the most effective prior therapy and country. The pairwise-censored groups were compared on hazards of 6-month confirmed EDSS worsening and improvement, relapses and annualised relapse rates (ARRs), using Andersen-Gill proportional hazards models and conditional negative binomial model.
39 patients treated with AHSCT (37 with secondary progressive MS, mean age 37 years, EDSS 5.7, 28% with recent disability progression, ARR 0.54 during the preceding year) were matched with 65 patients treated with natalizumab. The study found no evidence for difference in hazards of confirmed EDSS worsening (HR 1.49, 95% CI 0.70 to 3.14) and improvement (HR 1.50, 95% CI 0.22 to 10.29) between AHSCT and natalizumab over up to 4 years. The relapse activity was also similar while treated with AHSCT and natalizumab (ARR: mean±SD 0.08±0.28 vs 0.08±0.25; HR 1.05, 95% CI 0.39 to 2.82). In the AHSCT group, 3 patients experienced febrile neutropenia during mobilisation, 9 patients experienced serum sickness, 6 patients required intensive care unit admission and 36 patients experienced complications after discharge. No treatment-related deaths were reported.
This study does not support the use of AHSCT to control disability in progressive MS with advanced disability and low relapse activity.
那他珠单抗并未显示能改善进展性多发性硬化症(MS)的残疾状况。这项配对观察性研究比较了自体造血干细胞移植(AHSCT)与那他珠单抗在进展性 MS 中的疗效。
来自 7 个 AHSCT MS 中心和 MSBase 登记处的原发性/继发性进展性 MS 患者,接受 AHSCT 或那他珠单抗治疗,基于性别、年龄、扩展残疾状况量表(EDSS)、基线前 12/24 个月的复发次数、从 MS 发病到现在的时间、最有效的既往治疗和国家,采用倾向评分进行匹配。使用 Andersen-Gill 比例风险模型和条件负二项式模型,比较了 6 个月确认 EDSS 恶化和改善、复发和年复发率(ARR)的风险比。
39 名接受 AHSCT 治疗的患者(37 名患有继发性进展性 MS,平均年龄 37 岁,EDSS 5.7,28%有近期残疾进展,前一年 ARR 为 0.54)与 65 名接受那他珠单抗治疗的患者相匹配。研究发现,在长达 4 年的时间里,AHSCT 和那他珠单抗在确认 EDSS 恶化(HR 1.49,95%CI 0.70 至 3.14)和改善(HR 1.50,95%CI 0.22 至 10.29)方面的风险无差异。在接受 AHSCT 和那他珠单抗治疗时,复发活动也相似(ARR:均值±标准差 0.08±0.28 对 0.08±0.25;HR 1.05,95%CI 0.39 至 2.82)。在 AHSCT 组中,有 3 名患者在动员期间发生发热性中性粒细胞减少症,9 名患者发生血清病,6 名患者需要入住重症监护病房,36 名患者在出院后发生并发症。没有报告与治疗相关的死亡。
这项研究不支持在残疾状况严重且复发活动较低的进展性 MS 患者中使用 AHSCT 来控制残疾。