From the Department of Brain Sciences (R.S.N., A.M., A.S., P.M.), Faculty of Medicine, and Centre for Haematology (E.O., I.G.), Faculty of Medicine, Imperial College London; Imperial College Healthcare NHS Trust (R.S.N., O.M., V.S.-C., A.S., E.O., I.G., P.M.); Department of Neurology (E.E.R., E.S.), King's College Hospital, London, UK; Department of Neurosciences, Drug and Child Health (A.M.), University of Florence, Italy; Barts Health NHS Trust (B.T.); Department of Haematological Medicine (V.M., M.A.K.), King's College Hospital NHS Foundation Trust; Queen Square MS Centre (O.C.), Department of Neuroinflammation, UCL Queen Square Institute of Neurology, London, UK; Department of Health Sciences (DISSAL) (M.P.S.), University of Genova; and IRCCS Ospedale Policlinico San Martino (M.P.S.), Genova, Italy.
Neurology. 2021 Aug 31;97(9):e890-e901. doi: 10.1212/WNL.0000000000012449. Epub 2021 Jul 12.
To examine outcomes in people with multiple sclerosis (PwMS) treated with autologous hematopoietic stem cell transplantation (AHSCT) in a real-world setting.
This was a retrospective cohort study of PwMS treated with AHSCT at 2 centers in London, UK, consecutively between 2012 and 2019 who had ≥6 months of follow-up or died at any time. Primary outcomes were survival free of multiple sclerosis (MS) relapses, MRI new lesions, and worsening of Expanded Disability Status Scale (EDSS) score. Adverse events rates were also examined.
The cohort includes 120 PwMS; 52% had progressive MS (primary or secondary) and 48% had relapsing-remitting MS. At baseline, the median EDSS score was 6.0; 90% of the evaluable cases showed MRI activity in the 12 months preceding AHSCT. Median follow-up after AHSCT was 21 months (range 6-85 months). MS relapse-free survival was 93% at 2 years and 87% at 4 years after AHSCT. No new MRI lesions were detected in 90% of participants at 2 years and in 85% at 4 years. EDSS score progression-free survival (PFS) was 75% at 2 years and 65% at 4 years. Epstein-Barr virus reactivation and monoclonal paraproteinemia were associated with worse PFS. There were 3 transplantation-related deaths within 100 days (2.5%), all after fluid overload and cardiac or respiratory failure.
Efficacy outcomes of AHSCT in this real-world cohort are similar to those reported in more stringently selected clinical trial populations, although the risks may be higher.
This study is rated Class IV because of the uncontrolled, open-label design.
在真实环境中,检查多发性硬化症(MS)患者接受自体造血干细胞移植(AHSCT)治疗后的结果。
这是一项回顾性队列研究,纳入了 2012 年至 2019 年期间在英国伦敦的 2 家中心接受 AHSCT 治疗的 MS 患者,且随访时间≥6 个月或在任何时间死亡。主要结局是无 MS 复发、MRI 新病灶和扩展残疾状态量表(EDSS)评分恶化的生存情况。还检查了不良事件发生率。
队列包括 120 例 MS 患者;52%为进展型 MS(原发性或继发性),48%为复发缓解型 MS。基线时,EDSS 评分中位数为 6.0;90%的可评估病例在 AHSCT 前 12 个月内有 MRI 活动。AHSCT 后中位随访时间为 21 个月(范围 6-85 个月)。AHSCT 后 2 年和 4 年的 MS 无复发生存率分别为 93%和 87%。2 年内 90%的参与者和 4 年内 85%的参与者未检测到新的 MRI 病灶。EDSS 评分进展无进展生存率(PFS)分别为 2 年时为 75%和 4 年时为 65%。EBV 再激活和单克隆丙种球蛋白血症与较差的 PFS 相关。在 100 天内有 3 例移植相关死亡(2.5%),均发生在液体过载、心或呼吸衰竭后。
在这个真实世界队列中,AHSCT 的疗效与在更严格选择的临床试验人群中报告的结果相似,尽管风险可能更高。
由于该研究为非对照、开放性设计,因此被评为 IV 级。