Department of Medical Sciences and Public Health, Multiple Sclerosis Center, ATS Sardegna, Ospedale Binaghi, University of Cagliari, Via Is Guadazzonis 2, 09126, Cagliari, Italy.
Department of Medical Sciences and Public Health, Bone Marrow Transplant Center, University of Cagliari, Via Is Guadazzonis 2, 09126, Cagliari, Italy.
J Neurol. 2018 Feb;265(2):410-416. doi: 10.1007/s00415-017-8718-2. Epub 2017 Dec 21.
Autologous hematopoietic stem cell transplantation (aHSCT) is used in aggressive relapsing and progressive multiple sclerosis (MS). The multicentre studies and case series reported have relatively short follow-up.
To evaluate long-term effect and safety of HSCT in MS.
Patients referred to the MS centre of Cagliari and undergoing HSCT were included. Variations in relapses and EDSS before and after HSCT were evaluated by Wilcoxon test. A descriptive analysis was made for other clinical data.
Nine patients (female 6, males 3; 5 relapsing-remitting, 2 secondary progressive, 1 primary progressive, and 1 progressive relapsing) performed HSCT (1999-2006). The median follow-up was 11 years (11-18). Eight patients underwent aHSCT, seven using a low intensity conditioning regimen, and one an intermediate intensity. The primary progressive underwent allogeneic HSCT, due to onco hematological disease. The relapses number decreased in the 2 years following the procedure compared to the two preceding years (p = 0.041). New relapses or disease progressions were observed after a range of 7 (low intensity regimen)-118 (intermediate intensity) months. At last follow-up, the EDSS was stable in two patients, improved in two, and worse in five (maximum 2 EDSS in one patient). Six patients showed new lesions, and seven gadolinium-enhancing on brain MRI after a mean of 23.3 and 19.8 months, respectively. Two serious adverse events were reported: melanoma, and progressive multifocal leukoencephalopathy.
Our results confirm in a long follow-up the efficacy of HSCT in reducing relapses and disability progression. The risk/benefit profile is better for intermediate intensity regimens.
自体造血干细胞移植(aHSCT)用于侵袭性复发和进行性多发性硬化症(MS)。报告的多中心研究和病例系列随访时间相对较短。
评估 HSCT 在 MS 中的长期疗效和安全性。
纳入到卡利亚里 MS 中心接受 HSCT 的患者。采用 Wilcoxon 检验评估 HSCT 前后复发和 EDSS 的变化。对其他临床数据进行描述性分析。
9 例患者(女性 6 例,男性 3 例;5 例复发缓解型,2 例继发进展型,1 例原发进展型,1 例进展复发型)接受 HSCT(1999-2006 年)。中位随访时间为 11 年(11-18 年)。8 例患者接受 aHSCT,7 例采用低强度预处理方案,1 例采用中强度预处理方案。由于血液肿瘤疾病,1 例原发进展型患者接受异基因 HSCT。与预处理前 2 年相比,术后 2 年内复发次数减少(p=0.041)。预处理后 7(低强度方案)-118(中强度方案)个月时观察到新的复发或疾病进展。末次随访时,2 例患者 EDSS 稳定,2 例患者改善,5 例患者恶化(1 例患者 EDSS 增加 2 分)。6 例患者在脑 MRI 上显示新的病变,7 例患者显示钆增强。平均分别为 23.3 和 19.8 个月后。报告了 2 例严重不良事件:黑色素瘤和进行性多灶性白质脑病。
我们的结果在长期随访中证实了 HSCT 降低复发和残疾进展的疗效。中强度方案的风险/获益比更好。