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Autologous haematopoietic stem cell transplantation for aggressive multiple sclerosis: the Swedish experience.
Burman, Joachim; Iacobaeus, Ellen; Svenningsson, Anders; Lycke, Jan; Gunnarsson, Martin; Nilsson, Petra; Vrethem, Magnus; Fredrikson, Sten; Martin, Claes; Sandstedt, Anna; Uggla, Bertil; Lenhoff, Stig; Johansson, Jan-Erik; Isaksson, Cecilia; Hägglund, Hans; Carlson, Kristina; Fagius, Jan.
Afiliación
  • Burman J; Department of Neuroscience, Uppsala University, Uppsala, Sweden Department of Neurology, Uppsala University Hospital, Uppsala, Sweden.
  • Iacobaeus E; Neuroimmunology Unit, Department of Clinical Neuroscience, Karolinska Institute Solna, Center for Molecular Medicine, Stockholm, Sweden.
  • Svenningsson A; Department of Pharmacology and Clinical Neuroscience, Umeå University and University Hospital of Northern Sweden, Umeå, Sweden.
  • Lycke J; Department of Neurology, Institute of Neuroscience and Physiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Gunnarsson M; Department of Neurology, Örebro University Hospital, Örebro, Sweden School of Health and Medical Sciences, Örebro University, Örebro, Sweden.
  • Nilsson P; Department of Neurology, Skåne University Hospital Lund, Lund, Sweden.
  • Vrethem M; Neurology and Clinical Neurophysiology, Faculty of Health Sciences, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden Department of Neurology and Neurophysiology, County Council of Östergötland, Linköping, Sweden.
  • Fredrikson S; Department of Clinical Neuroscience, Karolinska Institute Huddinge, Stockholm, Sweden.
  • Martin C; Neurology Unit, Division of Internal Medicine, Danderyd Hospital, Karolinska Institute, Stockholm, Sweden.
  • Sandstedt A; Department of Hematology, Linköping University Hospital, Linköping, Sweden.
  • Uggla B; School of Health and Medical Sciences, Örebro University, Örebro, Sweden Division of Hematology, Department of Medicine, Örebro University Hospital, Örebro, Sweden.
  • Lenhoff S; Department of Hematology and Coagulation, Skåne University Hospital, Lund, Sweden.
  • Johansson JE; Department of Hematology and Coagulation, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Isaksson C; Department of Radiosciences, Umeå University, Umeå, Sweden.
  • Hägglund H; Division of Hematology, Department of Medical Science, Uppsala University Hospital, Uppsala, Sweden.
  • Carlson K; Division of Hematology, Department of Medical Science, Uppsala University Hospital, Uppsala, Sweden.
  • Fagius J; Department of Neuroscience, Uppsala University, Uppsala, Sweden Department of Neurology, Uppsala University Hospital, Uppsala, Sweden.
J Neurol Neurosurg Psychiatry ; 85(10): 1116-21, 2014 Oct.
Article en En | MEDLINE | ID: mdl-24554104
ABSTRACT

BACKGROUND:

Autologous haematopoietic stem cell transplantation (HSCT) is a viable option for treatment of aggressive multiple sclerosis (MS). No randomised controlled trial has been performed, and thus, experiences from systematic and sustained follow-up of treated patients constitute important information about safety and efficacy. In this observational study, we describe the characteristics and outcome of the Swedish patients treated with HSCT for MS.

METHODS:

Neurologists from the major hospitals in Sweden filled out a follow-up form with prospectively collected data. Fifty-two patients were identified in total; 48 were included in the study and evaluated for safety and side effects; 41 patients had at least 1 year of follow-up and were further analysed for clinical and radiological outcome. In this cohort, 34 patients (83%) had relapsing-remitting MS, and mean follow-up time was 47 months.

RESULTS:

At 5 years, relapse-free survival was 87%; MRI event-free survival 85%; expanded disability status scale (EDSS) score progression-free survival 77%; and disease-free survival (no relapses, no new MRI lesions and no EDSS progression) 68%. Presence of gadolinium-enhancing lesions prior to HSCT was associated with a favourable outcome (disease-free survival 79% vs 46%, p=0.028). There was no mortality. The most common long-term side effects were herpes zoster reactivation (15%) and thyroid disease (8.4%).

CONCLUSIONS:

HSCT is a very effective treatment of inflammatory active MS and can be performed with a high degree of safety at experienced centres.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante Autólogo / Encéfalo / Trasplante de Células Madre Hematopoyéticas / Esclerosis Múltiple Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Neurol Neurosurg Psychiatry Año: 2014 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante Autólogo / Encéfalo / Trasplante de Células Madre Hematopoyéticas / Esclerosis Múltiple Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Neurol Neurosurg Psychiatry Año: 2014 Tipo del documento: Article País de afiliación: Suecia