Autologous stem cell transplantation for progressive multiple sclerosis: Update of the European Group for Blood and Marrow Transplantation autoimmune diseases working party database

被引:165
作者
Saccardi, R.
Kozak, T.
Bocelli-Tyndall, C.
Fassas, A.
Kazis, A.
Havrdov, E.
Carreras, E.
Saiz, A.
Lowenberg, B.
te Boekhorst, P. A. W.
Gualandi, F.
Openshaw, H.
Longo, G.
Pagliai, F.
Massacesi, L.
Deconink, E.
Ouyang, J.
Nagore, F. J. Z.
Besalduch, J.
Lisukov, I. A.
Bonini, A.
Merelli, E.
Slavin, S.
Gratwahl, A.
Passweg, J.
Tyndall, A.
Steck, A. J.
Andolina, M.
Capobianco, M.
Martin, J. L. D.
Lugaresi, A.
Meucci, G.
Saez, R. A.
Clark, R. E.
Fernandez, M. N.
Fouillard, L.
Herstenstein, B.
Koza, V.
Cocco, E.
Baurmann, H.
Mancardi, G. L.
机构
[1] Osped Careggi, Dept Hematol, BMT Unit, Florence, Italy
[2] Charles Univ Prague, Sch Med 3, Dept Clin Hematol, Prague 10, Czech Republic
[3] Univ Basel Hosp, Dept Rheumatol, CH-4031 Basel, Switzerland
[4] George Papanicolaou Gen Hosp, BMT Unit, Dept Hematol, Thessaloniki, Greece
[5] George Papanicolaou Gen Hosp, Dept Neurol, Thessaloniki, Greece
[6] Charles Univ Prague, Sch Med 1, Dept Neurol, Prague 2, Czech Republic
[7] Hosp Clin Barcelona, Inst Hematol & Oncol, Dept Hematol, Barcelona, Spain
[8] Hosp Clin Barcelona, Lab Expt Neurol & Immunol, Barcelona, Spain
[9] Erasmus Univ, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[10] Osped San Martino Genova, Dept Hematol, Genoa, Italy
[11] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[12] Osped Careggi, Dept Neurol, Florence, Italy
[13] Hop Jean Minjoz, Serv Hematol, F-25030 Besancon, France
[14] Drum Tower Hosp, Dept Hematol, Nanjing, Peoples R China
[15] Hosp Gen Valle Hebron, Barcelona, Spain
[16] Hosp Univ Son Dureta, Hematol Serv, Palma de Mallorca, Spain
[17] Inst Clin Immunol, Novosibirsk, Russia
[18] Azienda Osped ASMN, Hematol Unit, Reggio Emilia, Italy
[19] Azienda Osped Policlin, Neurol Clin, Modena, Italy
[20] Hadassah Univ Hosp, Dept Bone Marrow Transplantat, IL-91120 Jerusalem, Israel
[21] Univ Basel Hosp, Dept Hematol, CH-4031 Basel, Switzerland
[22] Univ Basel Hosp, Dept Neurol, CH-4031 Basel, Switzerland
[23] Ist Infanzia Burlo Garofolo, Trieste, Italy
[24] Osped San Luigi Gonzaga, Turin, Italy
[25] Hosp Gen Gregorio Maranon, Secc Trasplante Medula Osea, Madrid, Spain
[26] Univ Gabriele Annunzio, Chieti, Italy
[27] Univ Hosp Pisa, Neurol Clin, Dept Neurosci, Pisa, Italy
[28] Hosp Princesa, Dept Hematol, Madrid, Spain
[29] Royal Liverpool Univ Hosp, Dept Haematol, Liverpool, Merseyside, England
[30] Clin Puerta de Hierro, Serv Hematol & Hemoterapia, Madrid, Spain
[31] Hop St Antoine, Dept Hematol, F-75571 Paris, France
[32] Hannover Med Univ, Dept Hematol Oncol, Hannover, Germany
[33] Charles Univ Hosp, Dept Hematol Oncol, Plzen, Czech Republic
[34] R Binaghi Hosp, Ctr Sclerosi Multipla, Cagliari, Italy
[35] Neurol & Klin Neurophysiol, Wiesbaden, Germany
[36] Univ Genoa, San Martino Hosp, Dept Neurosci Ophthalmol & Genet, Genoa, Italy
来源
MULTIPLE SCLEROSIS | 2006年 / 12卷 / 06期
关键词
autoimmune diseases; immunosuppression; multiple sclerosis; stem cells; transplantation; treatment safety;
D O I
10.1177/1352458506071301
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:814 / 823
页数:10
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