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Multiple Sclerosis, Vol. 12, No. 6,
814-823 (2006)
DOI: 10.1177/1352458506071301
© 2006 SAGE Publications
Autologous stem cell transplantation for progressive multiple sclerosis: Update of the European Group for Blood and Marrow Transplantation autoimmune diseases working party database
R Saccardi
BMT Unit Department of Hematology, Ospedale di Careggi, Florence, Italy
T Kozak
Department of Clinical Hematology, Third Medical School, Charles University, Prague 10, Czech Republic
C Bocelli-Tyndall
Department of Rheumatology, University Hospital, Basel, Switzerland
A Fassas
Hematology Department/BMT Unit, George Papanicolaou General Hospital, Thessaloniki, Greece
A Kazis
Department of Neurology, George Papanicolaou General Hospital, Thessaloniki, Greece
E Havrdova
Department of Neurology, First Medical School, Charles University, Prague 2, Czech Republic
E Carreras
Department of Hematology, Hospital Clinic, Institute of Hematology and Oncology, Barcelona, Spain
A Saiz
Laboratory of Experimental Neurology and Immunology, Hospital Clinic, Barcelona, Spain
B Löwenberg
Erasmus University Medical Center, Rotterdam, The Netherlands
P AW te Boekhorst
Erasmus University Medical Center, Rotterdam, The Netherlands
F Gualandi
Department of Hematology, San Martino Hospital, Genova, Italy
H Openshaw
City of Hope National Medical Center, Duarte, CA, USA
G Longo
BMT Unit Department of Hematology, Ospedale di Careggi, Florence, Italy
F Pagliai
BMT Unit Department of Hematology, Ospedale di Careggi, Florence, Italy
L Massacesi
Department of Neurology, Ospedale di Careggi, Florence, Italy
E Deconink
Service dHématologie, Hopital Jean Minjoz, Besançon, France
J Ouyang
Department of Hematology, Drum Tower Hospital, Nanjing, PR China
F JZ Nagore
Hospital Vall dHebron, Barcelona, Spain
J Besalduch
Hematology Service, Hospital Universitari Son Dureta, Palma de Mallorca, Spain
I A Lisukov
Institute of Clinical Immunology, Novosibirsk, Russia
A Bonini
Hematology Unit, Azienda Ospedaliera ASMN, Reggio Emilia, Italy
E Merelli
Clinica Neurologica, Azienda Ospedaliera Policlinico, Modena, Italy
S Slavin
Department of Bone Marrow Transplantation, Hadassah University Hospital, Jerusalem, Israel
A Gratwohl
Department of Hematology, University Hospital, Basel, Switzerland
J Passweg
Department of Hematology, University Hospital, Basel, Switzerland
A Tyndall
Department of Rheumatology, University Hospital, Basel, Switzerland
A J Steck
Department of Neurology, University Hospital, Basel, Switzerland
M Andolina
Istituto per lInfanzia Burlo Garofolo, Trieste, Italy
M Capobianco
Ospedale di San Luigi Gonzaga, Orbassano, Torino, Italy
J LD Martin
Sección de Trasplante de Medula Osea, Hospital Gregorio Marañón, Madrid, Spain
A Lugaresi
Università Gabriele dAnnunzio, Chieti, Italy
G Meucci
Department of Neuroscience, University Hospital of Pisa, Neurology Clinic, Pisa, Italy
R A Sáez
Department of Hematology, Hospital de la Princesa, Madrid, Spain
R E Clark
Department of Haematology, Royal Liverpool University Hospital, Liverpool, UK
M N Fernandez
Clinica Puerta de Hierro, Servicio de Hematologia y Hemoterapia, Madrid, Spain
L Fouillard
Department of Hematology, Hopital Saint Antoine, Paris, France
B Herstenstein
Department of Hematology/Oncology, Hannover Medical University, Hannover, Germany
V Koza
Department of Hematology/Oncology, Charles University Hospital, Pilsen, Czech Republic
E Cocco
R Binaghi Hospital, Centro Sclerosi Multipla, Cagliari, Italy
H Baurmann
Neurologie und Klinische Neurophysiologie, Wiesbaden, Germany
G L Mancardi
Department of Neuroscience, Ophthalmology and Genetics, San Martino Hospital, University of Genova, Genova, Italy
Autoimmune Diseases Working Party of EBMT
Over the last decade, hematopoietic stem cells transplantation (HSCT) has been increasingly used in the treatment of severe progressive autoimmune diseases. We report a retrospective survey of 183 multiple sclerosis (MS) patients, recorded in the database of the European Blood and Marrow Transplantation Group (EBMT). Transplant data were available from 178 patients who received an autologous graft. Overall, transplant related mortality (TRM) was 5.3% and was restricted to the period 1995-2000, with no further TRM reported since then. Busulphan-based regimens were significantly associated with TRM. Clinical status at the time of transplant and transplant techniques showed some correlations with toxicity. No toxic deaths were reported among the 53 patients treated with the BEAM (carmustine, etoposide, cytosine-arabinoside, melphalan)/antithymocyte globulin (ATG) regimen without graft manipulation, irrespective of their clinical condition at the time of the transplant. Improvement or stabilization of neurological conditions occurred in 63% of patients at a median follow-up of 41.7 months, and was not associated with the intensity of the conditioning regimen. In this large series, HSCT was shown as a promising procedure to slow down progression in a subset of patients affected by severe, progressive MS; the safety and feasibility of the procedure can be significantly improved by appropriate patient selection and choice of transplant regimen.
Key Words: autoimmune diseases immunosuppression multiple sclerosis stem cells transplantation treatment safety
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