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Autologous haematopoietic stem cell transplantation as a first-line disease-modifying therapy in patients with 'aggressive' multiple sclerosis.
Das, J; Snowden, J A; Burman, J; Freedman, M S; Atkins, H; Bowman, M; Burt, R K; Saccardi, R; Innocenti, C; Mistry, S; Laud, P J; Jessop, H; Sharrack, B.
Afiliação
  • Das J; Sheffield Institute for Translational Neuroscience, University of Sheffield, UK/Academic Department of Neurology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Snowden JA; Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Burman J; Department of Neurology, Uppsala University Hospital, Uppsala, Sweden.
  • Freedman MS; Department of Medicine (Neurology), The University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Atkins H; Department of Medicine (Neurology), The University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Bowman M; Department of Medicine (Neurology), The University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Burt RK; Division of Immunotherapy, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Saccardi R; Department of Cellular Therapies and Transfusion Medicine, Careggi University Hospital, Florence, Italy.
  • Innocenti C; Department of Cellular Therapies and Transfusion Medicine, Careggi University Hospital, Florence, Italy.
  • Mistry S; Academic Department of Neurology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Laud PJ; Statistical Services Unit, University of Sheffield, Sheffield, UK.
  • Jessop H; Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Sharrack B; Academic Department of Neurology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK; Sheffield Institute for Translational Neuroscience, University of Sheffield, UK.
Mult Scler ; 27(8): 1198-1204, 2021 07.
Article em En | MEDLINE | ID: mdl-33565902
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Esclerose Múltipla Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Mult Scler Assunto da revista: NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Esclerose Múltipla Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Mult Scler Assunto da revista: NEUROLOGIA Ano de publicação: 2021 Tipo de documento: Article