n | Age | MS subtype (n) | Disease duration (years) | EDSS | Conditioning | Follow-up time (months) | PFS | MRI | NEDA | TRM | Prognostic factors | ||||||||
RRMS | SPMS | PPMS | BEAM | Cy | Other | Timepoint | Percentage | Timepoint | Percentage | Timepoint | Percentage | Percentage | |||||||
Burman et al 37 | (41*) 48 | 31† | 34 | 5 | 2 | 5.5‡ | 6‡ | 34 | 6 | 47† | 60 | 77 | 60 | 85 | 60 | 68 | 0 | Gd+ at baseline | |
Nash et al 40 | 24 | 38‡ | 24 | 4.9‡ | 4.5‡ | 24 | 62‡ | 60 | 91 | 60 | 86 | 60 | 69 | 0 | |||||
Burt et al 38 | (145*) 151 | 37‡ | 118 | 27 | 61‡ | 4‡ | 145 | 30† | 48 | 87 | n/a | n/a | 48 | 68 | 0 | Disease duration <10 years RRMS vs SPMS fever in the peritransplant period | |||
Atkins et al 39 | 24 | 34‡ | 12 | 12 | 5.8‡ | 5‡ | 24 | 80‡ | 60 | 70 | 60 | 100 | 60 | 70 | 4.2 |
*Only evaluated for safety.
†Mean.
‡Median.
EDSS, expanded disability status score; HSCT, haematopoietic stem cell transplantation; MS, multiple sclerosis; NEDA, no evidence of disease activity; TRM, treatment-related mortality;RRMS, relapsing-remitting MS SPMS, secondary progressive MS; PPMS, primary progressive MS; PFS, progression-free survival; BEAM, the combination ofcarmustine (BCNU), etoposide, cytarabine (Ara-c), and melphalan; n/a, not available; Cy, cyclophosphamide40.