Autologous haematopoietic stem cell transplantation for multiple sclerosis: a position paper and registry outline

Author:

Bayas Antonios1,Berthele Achim2,Blank Norbert3,Dreger Peter4,Faissner Simon5,Friese Manuel A.6,Gerdes Lisa-Ann7,Grauer Oliver Martin8,Häussler Vivien9,Heesen Christoph1011ORCID,Janson Dietlinde12,Korporal-Kuhnke Mirjam13,Kowarik Markus14,Kröger Nikolaus12,Lünemann Jan D.15,Martin Roland16,Meier Uwe17,Meuth Sven18,Muraro Paolo19,Platten Michael20,Schirmer Lucas20,Stürner Klarissa Hanja21,Stellmann Jan Patrick22,Scheid Christof23,Bergh Florian Then24,Warnke Clemens25,Wildemann Brigitte13,Ziemssen Tjalf26

Affiliation:

1. Department of Neurology and Clinical Neurophysiology, Faculty of Medicine, University of Augsburg, Augsburg

2. Department of Neurology, School of Medicine, Technical University of Munich, Munich

3. Rheumatology Section, Interdisciplinary Centre for Chronic Inflammatory Diseases, Heidelberg University Hospital, Heidelberg

4. Spokesman German Working Group for Haematopoietic Stem Cell Transplantation and Cellular Therapy e.V., Heidelberg University Hospital, Heidelberg

5. Department of Neurology, University Hospital of Ruhr-University Bochum, St. Josef-Hospital, Bochum

6. Institute of Neuroimmunology and Multiple Sclerosis (INIMS) and Department of Neurology, University Medical Center Hamburg-Eppendorf

7. Institut für Klinische Neuroimmunologie am Klinikum der Ludwig-Maximilians-Universität München, München

8. Department of Neurology with Institute for Translational Neurology, University Hospital Münster, Münster

9. Institute of Neuroimmunology and Multiple Sclerosis (INIMS) and Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg

10. Institute of Neuroimmunology and Multiple Sclerosis (INIMS) and Department of Neurology University Medical Center Hamburg-Eppendorf

11. Clinical and Rehabilitative MS Research, Institute for Neuroimmunology and Multiple Sclerosis (INIMS), University Medical Center Hamburg-Eppendorf (UKE), Martinistrasse 52, D-20246 Hamburg, Germany

12. Clinic for Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg

13. AG Neuroimmunology, Neurological Clinic, Heidelberg University Hospital, Heidelberg

14. Department of Neurology & Stroke, and Hertie Institute for Clinical Brain Research, Eberhard-Karls University of Tübingen, Tübingen, Kröger

15. Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Münster

16. Institute of Experimental Neurology, University Hospital Zurich, Zurich, Switzerland

17. Chairman of the Professional Association of German Neurologists, Neurocentrum Grevenbroich, Grevenbroich

18. Medical Faculty, Department of Neurology, University Hospital Düsseldorf, Düsseldorf

19. Department of Brain Sciences, Imperial College London, London, UK

20. Department of Neurology, Mannheim Center for Translational Neuroscience, Medical Faculty Mannheim, Heidelberg University, Heidelberg

21. Department of Neurology, Christian-Albrechts-Universität Kiel, Kiel

22. Centre de Résonance Magnétique Biologique et Médicale, Aix-Marseille Université, Marseille

23. Clinic I for Internal Medicine, University Hospital Cologne, Cologne

24. Clinic and Polyclinic for Neurology, University of Leipzig, Leipzig

25. University of Cologne, Faculty of Medicine and University Hospital Cologne, Clinic and Polyclinic of Neurology, Cologne

26. Center of Clinical Neuroscience, Department of Neurology, University Clinic Carl Gustav Carus Dresden, Technische Universität Dresden

Abstract

Background: While substantial progress has been made in the development of disease-modifying medications for multiple sclerosis (MS), a high percentage of treated patients still show progression and persistent inflammatory activity. Autologous haematopoietic stem cell transplantation (AHSCT) aims at eliminating a pathogenic immune repertoire through intense short-term immunosuppression that enables subsequent regeneration of a new and healthy immune system to re-establish immune tolerance for a long period of time. A number of mostly open-label, uncontrolled studies conducted over the past 20 years collected about 4000 cases. They uniformly reported high efficacy of AHSCT in controlling MS inflammatory disease activity, more markedly beneficial in relapsing-remitting MS. Immunological studies provided evidence for qualitative immune resetting following AHSCT. These data and improved safety profiles of transplantation procedures spurred interest in using AHSCT as a treatment option for MS. Objective: To develop expert consensus recommendations on AHSCT in Germany and outline a registry study project. Methods: An open call among MS neurologists as well as among experts in stem cell transplantation in Germany started in December 2021 to join a series of virtual meetings. Results: We provide a consensus-based opinion paper authored by 25 experts on the up-to-date optimal use of AHSCT in managing MS based on the Swiss criteria. Current data indicate that patients who are most likely to benefit from AHSCT have relapsing-remitting MS and are young, ambulatory and have high disease activity. Treatment data with AHSCT will be collected within the German REgistry Cohort of autologous haematopoietic stem CeLl trAnsplantation In MS (RECLAIM). Conclusion: Further clinical trials, including registry-based analyses, are urgently needed to better define the patient characteristics, efficacy and safety profile of AHSCT compared with other high-efficacy therapies and to optimally position it as a treatment option in different MS disease stages.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology,Pharmacology

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