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Autologous haematopoietic stem cell transplantation as a first-line disease-modifying therapy in patients with 'aggressive' multiple sclerosis

Das, J. (författare)
Royal Hallamshire Hosp, Sheffield Teaching Hosp NHS Fdn Trust, Acad Dept Neurol, Glossop Rd, Sheffield, S Yorkshire, England; Univ Sheffield, Sheffield Teaching Hosp NHS Fdn Trust, Sheffield Inst Translat Neurosci, UK Acad Dept Neurol, Sheffield, S Yorkshire, England
Snowden, J. A. (författare)
Sheffield Teaching Hosp NHS Fdn Trust, Dept Haematol, Sheffield, S Yorkshire, England
Burman, Joachim, 1974- (författare)
Uppsala universitet,Landtblom: Neurovetenskap
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Freedman, M. S. (författare)
Univ Ottawa, Dept Med Neurol, Ottawa, ON, Canada; Ottawa Hosp Res Inst, Ottawa, ON, Canada
Atkins, H. (författare)
Univ Ottawa, Dept Med Neurol, Ottawa, ON, Canada; Ottawa Hosp Res Inst, Ottawa, ON, Canada
Bowman, M. (författare)
Univ Ottawa, Dept Med Neurol, Ottawa, ON, Canada; Ottawa Hosp Res Inst, Ottawa, ON, Canada
Burt, R. K. (författare)
Northwestern Univ, Feinberg Sch Med, Div Immunotherapy, Chicago, IL 60611 USA
Saccardi, R. (författare)
Careggi Univ Hosp, Dept Cellular Therapies & Transfus Med, Florence, Italy
Innocenti, C. (författare)
Careggi Univ Hosp, Dept Cellular Therapies & Transfus Med, Florence, Italy
Mistry, S. (författare)
Sheffield Teaching Hosp NHS Fdn Trust, Acad Dept Neurol, Sheffield, S Yorkshire, England
Laud, P. J. (författare)
Univ Sheffield, Stat Serv Unit, Sheffield, S Yorkshire, England
Jessop, H. (författare)
Sheffield Teaching Hosp NHS Fdn Trust, Dept Haematol, Sheffield, S Yorkshire, England
Sharrack, B. (författare)
Sheffield Teaching Hosp NHS Fdn Trust, Acad Dept Neurol, Sheffield, S Yorkshire, England; Univ Sheffield, Sheffield Inst Translat Neurosci, Sheffield, S Yorkshire, England
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 (creator_code:org_t)
2021-02-10
2021
Engelska.
Ingår i: Multiple Sclerosis Journal. - : SAGE Publications. - 1352-4585 .- 1477-0970. ; 27:8, s. 1198-1204
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background:Autologous haematopoietic stem cell transplantation (AHSCT) is an effective treatment for patients with multiple sclerosis (MS) who have highly active disease, despite the use of standard disease-modifying therapies (DMTs). However, the optimal time for offering AHSCT to patients with ‘aggressive’ MS is yet to be established.Objectives:The objective was to explore the safety and efficacy of AHSCT as a first-line DMT in patients with ‘aggressive’ MS.Methods:All patients with ‘aggressive’ MS who received AHSCT as a first-line DMT in five European and North American centres were retrospectively evaluated.Results:Twenty patients were identified. The median interval between diagnosis and AHSCT was 5 (1–20) months. All had multiple poor prognostic markers with a median pre-transplant Expanded Disability Status Scale (EDSS) score of 5.0 (1.5–9.5). After a median follow-up of 30 (12–118) months, the median EDSS score improved to 2.0 (0–6.5, p < 0.0001). No patient had further relapses. Three had residual magnetic resonance imaging (MRI) disease activities in the first 6 months post-transplant, but no further new or enhancing lesions were observed in subsequent scans.Conclusion:AHSCT is safe and effective as a first-line DMT in inducing rapid and sustained remission in patients with ‘aggressive’ MS.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

Autologous haematopoietic stem cell transplantation
multiple sclerosis
aggressive multiple sclerosis
disease-modifying therapy
no evidence of disease activity

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