Early highly aggressive MS successfully treated by hematopoietic stem cell transplantation

被引:62
作者
Fagius, J. [1 ]
Lundgren, J. [2 ]
Oberg, G. [3 ]
机构
[1] Univ Uppsala Hosp, Dept Neurol, SE-75185 Uppsala, Sweden
[2] Univ Lund Hosp, Dept Paediat, S-22185 Lund, Sweden
[3] Univ Uppsala Hosp, Dept Haematol, SE-75185 Uppsala, Sweden
来源
MULTIPLE SCLEROSIS | 2009年 / 15卷 / 02期
关键词
early MS; high-dose chemotherapy; HSCT; hematopoietic stem cell transplantation; malignant MS; relapsing-remitting MS; PROGRESSIVE MULTIPLE-SCLEROSIS; MARROW-TRANSPLANTATION; AUTOIMMUNE-DISEASES; EUROPEAN GROUP; BLOOD; MULTICENTER; GUIDELINES; NEUROLOGY; THERAPY;
D O I
10.1177/1352458508096875
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Background During the last 15 years, high-dose chemotherapy with autologous hematopoietic stem cell transplantation (HSCT) has globally been performed for severe multiple sclerosis (MS). Most patients have been in progressive phase with long disease duration. As a rule, treatment effect has been minor or moderate. Patients Since 2004, we have performed HSCT in nine young patients with "malignant" relapsing remitting MS. Criteria for treatment were short duration of disease; very frequent, severe relapses; recent improvement periods indicating potential for recovery after strong immunosuppression. Findings Median age at treatment was 27 (range 9-34) years, MS duration 26 (4-100) months, and annualized relapse rate 10 (4-12). Median Disability Status Scale (extended disability status scale, EDSS) at HSCT was 7.0 (3.5-8.0). Median follow-up time April 2008 is 29 (23-47) months. Median EDSS improvement is 3.5 (1.0-7.0), clearly surpassing most previous reports. One patient relapsed mildly with rapid recovery 7 months after HSCT. All patients are otherwise stable, median EDSS being 2.0 (0-6.0). Before HSCT, 61 relapses occurred in 82 patient months; during follow-up, one relapse in 289 patient months. Conclusion This small series of patients with "malignant" relapsing-remitting MS suggests HSCT to be an effective treatment option for this relatively rare disease course. It further suggests that future criteria for HSCT in MS should be close to the present ones. Multiple Sclerosis 2009; 15: 229-237. http://msj.sagepub.com
引用
收藏
页码:229 / 237
页数:9
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