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

Author:

Das J1ORCID,Snowden JA2,Burman J3ORCID,Freedman MS4,Atkins H4,Bowman M4,Burt RK5,Saccardi R6,Innocenti C6,Mistry S7ORCID,Laud PJ8,Jessop H2,Sharrack B9

Affiliation:

1. Sheffield Institute for Translational Neuroscience, University of Sheffield, UK/Academic Department of Neurology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK

2. Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK

3. Department of Neurology, Uppsala University Hospital, Uppsala, Sweden

4. Department of Medicine (Neurology), The University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, ON, Canada

5. Division of Immunotherapy, Northwestern University Feinberg School of Medicine, Chicago, IL, USA

6. Department of Cellular Therapies and Transfusion Medicine, Careggi University Hospital, Florence, Italy

7. Academic Department of Neurology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK

8. Statistical Services Unit, University of Sheffield, Sheffield, UK

9. Academic Department of Neurology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK; Sheffield Institute for Translational Neuroscience, University of Sheffield, UK

Abstract

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.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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