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. 2016 Dec 23;187(3):383–398. doi: 10.1111/cei.12895

Table 1.

Clinical data from multiple sclerosis patients before and after autologous haematopoietic stem cell transplantation

Controls gender/age (years) Patients gender/age (years) MS subtypes Disease duration (years) EDSS pre‐AHSCT EDSS day + 180/ day + 360/day+ 720 post‐AHSCT MRI pre‐AHSCT/post‐AHSCT Previous therapy Clinical response at day + 720 post‐AHSCT
M/37 M/37 SP 14 6·5 6·5/6·5/6·0 Inactivity/inactivity STER/IFN/GA Non‐progression
M/48 M/52 SP 09 6·5 6·0/6·0/7·5 Inactivity/n.d. STER/IFN/GA Progression
M/52 M/50 SP 09 6·5 8·0/7·5/7·5 Inactivity/inactivity STER/IFN/GA Progression
F/42 F/43 SP 12 6·5 8·0/7·5/7·5 Inactivity/inactivity STER/IFN/GA Progression
F/42 F/42 SP 11 7·0 7·0/9·0/9·0 Inactivity/n.d. STER/IFN/GA Progression
M/20 M/31 PP 04 6·5 6·5/6·5/6·5 Activity/inactivity STER/IFN/GA Non‐progression
M/54 M/52 PP 11 6·5 6·5/6·5/7·5 Inactivity/n.d. STER/IFN/GA Progression
F/47 F/44 SP 20 6·5 6·5/6·5/6·5 Inactivity/inactivity STER/IFN/GA Non‐progression
F/48 F/48 SP 10 4·5 2·5/3·0/3·0 Inactivity/inactivity STER/IFN/GA Non‐progression
M/55 M/54 SP 09 6·5 6·5/6·0/6·0 Inactivity/inactivity STER/IFN/GA Non‐progression
F/33 F/36 SP 14 6·5 6·5/7·0/8·0 Inactivity/inactivity STER/IFN/GA Progression
F/32 F/32 SP 06 6·0 6·0/6·0/6·0 Inactivity/inactivity STER/IFN/GA Non‐progression
F/40 F/42 SP 10 6·0 6·0/6·0/6·0 Inactivity/inactivity STER/IFN/GA Non‐progression
M/47 M/49 PP 10 6·5 6·5/6·5/6·5 Inactivity/inactivity STER/IFN/GA Non‐progression
F/36 F/38 PP 09 6·5 6·5/6·5/6·5 Inactivity/inactivity STER/IFN/GA Non‐progression
F/36 F/36 SP 11 5·0 2·5/2·5/2·5 Inactivity/inactivity STER/IFN/GA Non‐progression
M/33 M/33 SP 11 6·5 6·5/6·5/7·0 Activity/inactivity STER/IFN/GA Progression
F/30 F/31 SP 06 6·5 5·5/5·0/4·5 Activity/inactivity STER/IFN/GA Non‐progression

M = male; F = female; MS = multiple sclerosis; SP = secondary progressive; PP = primary progressive; EDSS = expanded disability status scale; MRI = magnetic resonance imaging; activity = contrast enhancement of any lesion; inactivity = no contrast enhancement; n.d. = not determined; STER = intravenous (i.v.) corticosteroids; IFN = β interferon; GA = glatiramer acetate. Progression or improvement was considered when the EDSS scores, respectively, increased or decreased by 0·5 points when the initial score was ≥ 5.5 or by 1·0 or more points if the initial score was < 5·0, remaining unchanged for at least 3 months. Patients were treated with BCNU, Etoposide, AraC and Melphalan/horse anti‐human thymocyte globulin (BEAM/hATG) (BEAM group; patients 1–7) or cyclophosphamide/rabbit ATG (CY/rATG) (CY group; patients 8–18) conditioning regimens. Based on EDSS changes after autologous haematopoietic stem cell transplantation (AHSCT), from baseline to last visit, patients were classified, retrospectively, as: progression = patients who presented an increase in the EDSS scores; non‐progression = patients whose EDSS scores either decreased or remained stable.