A prospective, randomized, controlled trial of autologous haematopoietic stem cell transplantation for aggressive multiple sclerosis: a position paper

Author:

Saccardi R1,Freedman MS2,Sormani MP3,Atkins H4,Farge D5,Griffith LM6,Kraft G7,Mancardi GL8,Nash R9,Pasquini M10,Martin R11,Muraro PA12

Affiliation:

1. Hematology Department, Careggi University Hospital, Florence, Italy

2. Department of Medicine (Neurology), University of Ottawa and the Ottawa Hospital Research Institute, Canada

3. Department of Health Sciences, University of Genoa, Italy

4. The Ottawa Hospital Blood and Marrow Transplant Programme, The Ottawa Hospital, Canada

5. Internal Medicine Department, Saint Louis Hospital, Paris, France

6. Division of Allergy, Immunology and Transplantation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, USA

7. Department of Rehabilitation Medicine, University of Washington, USA

8. Department of Neuroscience, Ophthalmology and Genetics, University of Genoa, Italy

9. Clinical Research Division, Fred Hutchinson Cancer Research Center, and University of Washington, USA

10. Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, USA

11. Department of Clinical Neuroimmunology and MS Research, Neurology Clinic, University Hospital Zürich, Switzerland

12. Centre for Neuroscience, Imperial College London, UK

Abstract

Background: Haematopoietic stem cell transplantation (HSCT) has been tried in the last 15 years as a therapeutic option in patients with poor-prognosis autoimmune disease who do not respond to conventional treatments. Worldwide, more than 600 patients with multiple sclerosis (MS) have been treated with HSCT, most of them having been recruited in small, single-centre, phase 1–2 uncontrolled trials. Clinical and magnetic resonance imaging outcomes from case series reports or Registry-based analyses suggest that a major response is achieved in most patients; quality and duration of response are better in patients transplanted during the relapsing–remitting phase than in those in the secondary progressive stage. Objectives: An interdisciplinary group of neurologists and haematologists has been formed, following two international meetings supported by the European and American Blood and Marrow Transplantation Societies, for the purpose of discussing a controlled clinical trial, to be designed within the new scenarios of evolving MS treatments. Conclusions: Objectives of the trial, patient selection, transplant technology and outcome assessment were extensively discussed. The outcome of this process is summarized in the present paper, with the goal of establishing the background and advancing the development of a prospective, randomized, controlled multicentre trial to assess the clinical efficacy of HSCT for the treatment of highly active MS.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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