Autologous stem cell transplantation in the treatment of systemic sclerosis:: report from the EBMT/EULAR Registry

被引:177
作者
Farge, D
Passweg, J
van Laar, JM
Marjanovic, Z
Besenthal, C
Finke, J
Peter, HH
Breedveld, FC
Fibbe, WE
Black, C
Denton, C
Koetter, I
Locatelli, F
Martini, A
Schattenberg, AVN
van den Hoogen, F
van de Putte, L
Lanza, F
Arnold, R
Bacon, PA
Bingham, S
Ciceri, F
Didier, B
Diez-Martin, JL
Emery, P
Feremans, W
Hertenstein, B
Hiepe, F
Luosujärvi, R
Lara, AL
Marmont, A
Martinez, AM
Cascon, HP
Bocelli-Tyndall, C
Gluckman, E
Gratwohl, A
Tyndall, A
机构
[1] Hop St Louis, Serv Med Interne, F-75010 Paris, France
[2] Acad Hosp Leiden, Leiden, Netherlands
[3] Univ Freiburg, Freiburg, Germany
[4] Carlos Haya Hosp, Malaga, Spain
[5] Charite Hosp, Berlin, Germany
[6] Free Univ Brussels, Erasme Hosp, B-1050 Brussels, Belgium
[7] Hosp SAS, Jerez de la Frontera, Cadiz, Spain
[8] Hosp GU Gregorio Maranon, Madrid, Spain
[9] Hosp Infantil La Paz, Madrid, Spain
[10] Inst Paoli Calmettes, Marseille, France
[11] IRCCS, Genoa, Italy
[12] Kantonsspital, CH-4031 Basel, Switzerland
[13] Hannover Med Sch, Hannover, Germany
[14] Osped San Martino Genova, Genoa, Italy
[15] Royal Free Hosp, London NW3 2QG, England
[16] San Matteo Univ Hosp, Pavia, Italy
[17] Hosp San Raffaele, I-20132 Milan, Italy
[18] St Anna Univ Hosp, Ferrara, Italy
[19] Univ Klinikum, Tubingen, Germany
[20] Univ Hosp, Leeds, W Yorkshire, England
[21] Univ Hosp, Birmingham, W Midlands, England
[22] Univ Hosp, Nijmegen, Netherlands
[23] Univ Hosp, Kuopio, Finland
关键词
D O I
10.1136/ard.2003.011205
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To analyse the durability of the responses after haematopoietic stem cell transplantation (HSCT) for severe systemic sclerosis (SSc) and determine whether the high transplant related mortality (TRM) improved with experience. This EBMT/EULAR report describes the longer outcome of patients originally described in addition to newly recruited cases. Methods: Only patients with SSc, treated by HSCT in European phase I-II studies from 1996 up to 2002, with more than 6 months of follow up were included. Transplant regimens were according to the international consensus statements. Repeated evaluations analysed complete, partial, or non-response and the probability of disease progression and survival after HSCT (Kaplan-Meier). Results: Given as median ( range). Among 57 patients aged 40 (9.1-68.7) years the skin scores improved at 6 (n = 37 patients), 12 ( n = 30), 24 ( n = 19), and 36 ( n = 10) months after HSCT (p<0.005). After 22.9 (4.5-81.1) months, partial (n = 32) or complete response (n = 14) was seen in 92% and non-response in 8% (n = 4) of 50 observed cases. 35% of the patients with initial partial (n = 13/32) or complete response (n = 3/14) relapsed within 10 (2.2-48.7) months after HSCT. The TRM was 8.7% (n = 5/57). Deaths related to progression accounted for 14% (n = 8/57) of the 23% (n = 13/57) total mortality rate. At 5 years, progression probability was 48% (95% CI 28 to 68) and the projected survival was 72% ( 95% CI 59 to 75). Conclusion: This EBMT/EULAR report showed that response in two thirds of the patients after HSCT was durable with an acceptable TRM. Based on these results prospective, randomised trials are proceeding.
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页码:974 / 981
页数:8
相关论文
共 68 条
[51]  
2-U
[52]  
Storb R, 1997, J RHEUMATOL, V24, P30
[53]   Pilot study of anti-thymocyte globulin plus mycophenolate mofetil in recent-onset diffuse scleroderma [J].
Stratton, RJ ;
Wilson, H ;
Black, CM .
RHEUMATOLOGY, 2001, 40 (01) :84-88
[54]   Treatment of severe systemic lupus erythematosus with high-dose chemotherapy and haemopoietic stem-cell transplantation: a phase I study [J].
Traynor, AE ;
Schroeder, J ;
Rosa, RM ;
Cheng, D ;
Stefka, J ;
Mujais, S ;
Baker, S ;
Burt, RK .
LANCET, 2000, 356 (9231) :701-707
[55]   Blood and marrow stem cell transplants in auto-immune disease: A consensus report written on behalf of the European League against Rheumatism (EULAR) and the European Group for Blood and Marrow Transplantation (EBMT) [J].
Tyndall, A ;
Gratwohl, A .
BONE MARROW TRANSPLANTATION, 1997, 19 (07) :643-645
[56]   Autologous haematopoietic stem cell transplants for autoimmune disease -: feasibility and transplant-related mortality [J].
Tyndall, A ;
Fassas, A ;
Passweg, J ;
de Elvira, CR ;
Attal, M ;
Brooks, P ;
Black, C ;
Durez, P ;
Finke, J ;
Forman, S ;
Fouillard, L ;
Furst, D ;
Holmes, JA ;
Joske, D ;
Jouet, JP ;
Kötter, I ;
Locatelli, F ;
Prentice, HG ;
Marmont, AM ;
McSweeney, P ;
Musso, M ;
Peter, HH ;
Snowden, JA ;
Sullivan, K ;
Tichelli, A ;
Vavriec, J ;
Wulffraat, NM ;
Schmitz, N ;
Gratwohl, A .
BONE MARROW TRANSPLANTATION, 1999, 24 (07) :729-734
[57]   Immune ablation and stem-cell therapy in autoimmune disease - Clinical experience [J].
Tyndall, A ;
Gratwohl, A .
ARTHRITIS RESEARCH, 2000, 2 (04) :276-280
[58]   Haemopoietic stem and progenitor cells in the treatment of severe autoimmune diseases [J].
Tyndall, A ;
Gratwohl, A .
ANNALS OF THE RHEUMATIC DISEASES, 1996, 55 (03) :149-151
[59]   New opportunities for the treatment of severe autoimmune diseases: Bone marrow transplantation [J].
van Bekkum, DW .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 89 (01) :1-10
[60]  
vandePutte LBA, 1997, J RHEUMATOL, V24, P98