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Journal of Neurology

, Volume 249, Issue 8, pp 1088–1097 | Cite as

Hematopoietic stem cell transplantation for multiple sclerosis

A retrospective multicenter study
  • A.S. Fassas
  • J. R. Passweg
  • A. Anagnostopoulos
  • A. Kazis
  • T. Kozak
  • E. Havrdova
  • E. Carreras
  • F. Graus
  • A. Kashyap
  • H. Openshaw
  • M. Schipperus
  • E. Deconinck
  • G. Mancardi
  • A. Marmont
  • J. Hansz
  • M. Rabusin
  • F. J. Zuazu Nagore
  • J. Besalduch
  • T. Dentamaro
  • L. Fouillard
  • B. Hertenstein
  • G. La Nasa
  • M. Musso
  • F. Papineschi
  • J. M. Rowe
  • R. Saccardi
  • A. Steck
  • L. Kappos
  • A. Gratwohl
  • A. Tyndall
  • for the Autoimmune Disease Working Party of the EBMT (European Group for Blood and Marrow Transplantation)
ORIGINAL COMMUNICATION

Abstract

Rationale Phase I/II studies of autologous hematopoietic stem cell transplantation (HSCT) for multiple sclerosis (MS) were initiated, based on results of experimental transplantation in animal models of multiple sclerosis and clinical observations in patients treated concomitantly for malignant disease. Patients Eighty-five patients with progressive MS were treated with autologous HSCT in 20 centers and reported to the autoimmune disease working party of the European Group for Blood and Marrow Transplantation (EBMT). 52 (61 %) were female, median age was 39 [20-58] years. The median interval from diagnosis to transplant was 7 [1-26] years. Patients suffered from severe disease with a median EDSS score of 6.5 [4.5-8.5]. Active disease prior to transplant was documented in 79 of 82 evaluable cases. Results The stem cell source was bone marrow in 6 and peripheral blood in 79, and stem cells were mobilized into peripheral blood using either cyclophosphamide combined with growth factors or growth factors alone. Three patients experienced transient neurological complications during the mobilization phase. The high dose regimen included combination chemotherapy, with or without anti-lymphocyte antibodies or, with or without, total body irradiation. The stem cell transplants were purged of lymphocytes in 52 patients. Median follow-up was 16 [3-59] months. There were 7 deaths, 5 due to toxicity and infectious complications, 2 with neurological deterioration. The risk of death of any cause at 3 years was 10 (±7)% (95 % confidence interval). Neurological deterioration during transplant was observed in 22 patients; this was transient in most but was associated with MS progression in 6 patients. Neurological improvement by ≥ 1 point in the EDSS score was seen in 18 (21 %) patients. Confirmed progression-free survival was 74 (±12)% at 3 years being 66 (±23)% in patients with primary progressive MS but higher in patients with secondary progressive or relapsing-remitting MS, 78 (±13)%; p = 0.59. The probability of confirmed disease progression was 20 (±11)%. MRI data were available in 78 patients before transplant showing disease activity (gadolinium enhancing, new or enlarging lesions) in 33 %. Posttransplant MRI showed activity at any time in 5/61 (8 %) evaluable cases. Conclusion Autologous HSCT suggest positive early results in the management of progressive MS and is feasible. These multicentre data suggest an association with significant mortality risks especially in some patient groups and are being utilised in the planning of future trials to reduce transplant related mortality.

Key words multiple sclerosis hematopoietic stem cell transplantation 

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Copyright information

© Steinkopff Verlag 2002

Authors and Affiliations

  • A.S. Fassas
    • 20
  • J. R. Passweg
    • 19
  • A. Anagnostopoulos
    • 20
  • A. Kazis
    • 20
  • T. Kozak
    • 1
  • E. Havrdova
    • 1
  • E. Carreras
    • 2
  • F. Graus
    • 2
  • A. Kashyap
    • 3
  • H. Openshaw
    • 3
  • M. Schipperus
    • 4
  • E. Deconinck
    • 5
  • G. Mancardi
    • 6
  • A. Marmont
    • 6
  • J. Hansz
    • 7
  • M. Rabusin
    • 8
  • F. J. Zuazu Nagore
    • 9
  • J. Besalduch
    • 10
  • T. Dentamaro
    • 11
  • L. Fouillard
    • 12
  • B. Hertenstein
    • 13
  • G. La Nasa
    • 14
  • M. Musso
    • 15
  • F. Papineschi
    • 16
  • J. M. Rowe
    • 17
  • R. Saccardi
    • 18
  • A. Steck
    • 19
  • L. Kappos
    • 19
  • A. Gratwohl
    • 19
  • A. Tyndall
    • 19
  • for the Autoimmune Disease Working Party of the EBMT (European Group for Blood and Marrow Transplantation)
  1. 1.Charles University Prague, Czech RepublicCZ
  2. 2.Hospital Clinic, Barcelona, SpainES
  3. 3.City of Hope Medical Center Duarte, CA, USAUS
  4. 4.University Hospital Rotterdam, the NetherlandsNL
  5. 5.Hôpital J. Minjoz Besançon, FranceFR
  6. 6.Ospedale S. Martino Genova, ItalyIT
  7. 7.Marcinkowski University Poznan, PolandPL
  8. 8.Instituto per l'Infanzia Trieste, ItalyIT
  9. 9.Hospital Vall d'Hebron Barcelona, SpainES
  10. 10.Hospital Son Dureta Palma de Mallorca, SpainES
  11. 11.University Tor Vergata Roma, ItalyIT
  12. 12.Hôpital St. Antoine Paris, FranceFR
  13. 13.Hannover Medical University, GermanyDE
  14. 14.Ospedali Binaghi, Centro Sclerosi Multipla University of Cagliari, ItalyIT
  15. 15.Ospedale la Maddalena Palermo, ItalyIT
  16. 16.Azienda Ospedaliera Pisa, ItalyIT
  17. 17.Rambam Medical Center Haifa, IsraelIL
  18. 18.Azienda Ospedaliera Careggi Firenze, ItalyIT
  19. 19.Kantonsspital Basel, SwitzerlandCH
  20. 20.George Papanicolaou General Hospital Dpt. Hematology 57010 Thessaloniki, Greece E-Mail: hempap@otenet.grGR

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