Allogeneic hematopoietic SCT for patients with autoimmune diseases

被引:71
作者
Daikeler, T. [1 ]
Huegle, T. [1 ]
Farge, D. [2 ,3 ]
Andolina, M. [4 ]
Gualandi, F. [5 ]
Baldomero, H. [6 ]
Bocelli-Tyndall, C. [1 ]
Brune, M. [7 ]
Dalle, J. H. [8 ]
Ehninger, G. [9 ]
Gibson, B. [10 ]
Linder, B. [11 ]
Lioure, B. [12 ]
Marmont, A. [5 ]
Matthes-Martin, S. [13 ]
Nachbaur, D. [14 ]
Schuetz, P. [15 ]
Tyndall, A. [1 ]
van Laar, J. M. [16 ]
Veys, P. [17 ]
Saccardi, R. [18 ]
Gratwohl, A. [6 ]
机构
[1] Univ Basel, Dept Rheumatol, Univ Basel Hosp, CH-4031 Basel, Switzerland
[2] Univ Paris 07, Dept Internal Med, Paris, France
[3] Univ Paris 07, INSERM, U Paris 697, Hop St Louis, Paris, France
[4] Ctr Trapianti Clin Pediat Trieste, Ist Infanzia Burlo Garofolo, Trieste, Italy
[5] San Martino Hosp, Dept Hematol, Genoa, Italy
[6] Univ Basel, Dept Med, Univ Hosp, Basel, Switzerland
[7] Sahlgrens Univ Hosp, Hematol Sect, Gothenburg, Sweden
[8] Hop Robert Debre, Haematol & Immunol Paediat Unit, F-75019 Paris, France
[9] Univ Klinikum Carl Gustav Carus, Klin & Poliklin Kinder & Jugendmed, Dresden, Germany
[10] Royal Hosp Sick Children, Dept Haematol, Glasgow G3 8SJ, Lanark, Scotland
[11] Univ Hosp, Dept Internal Med, Innsbruck, Austria
[12] Univ Hosp, Dept Hematol & Oncol, Strasbourg, France
[13] St Anna Childrens Hosp, BMT Unit, Vienna, Austria
[14] Univ Hosp, Dept Hematol & Oncol, Innsbruck, Austria
[15] Univ Basel, Dept Med, Univ Basel Hosp, CH-4031 Basel, Switzerland
[16] Univ Newcastle, Musculoskeletal Res Grp, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
[17] Great Ormond St Hosp London, Dept Clin Immunol, London, England
[18] Careggi Hosp, Hematol Unit, Florence, Italy
基金
新加坡国家研究基金会;
关键词
autoimmune diseases; allogeneic; SCT; STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; RHEUMATOID-ARTHRITIS; FOLLOW-UP; ANEMIA; MICE;
D O I
10.1038/bmt.2008.424
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Allogeneic hematopoietic SCT (HSCT) ha s been used as treatment for single patients with autoimmune diseases (AD). To summarise currently available information, we analyzed all patients who underwent allogeneic HSCT for AD and who reported to the European Group for Blood and Marrow Transplantation (EBMT) data base. Thirty-five patients receiving 38 allogeneic transplantations for various hematological and non-hematological AD were identified. Four patients had had an allogeneic HSCT for a conventional hematological indication in the past. Fifty-five per cent of the transplantation procedures led to a complete clinical response of the refractory AD and 23% to at least a partial response. The median duration of response at the last follow-up was 70.7 (15.2-130) months. Three patients relapsed at a median of 12.3 months after HSCT. Treatment-related mortality at 2 years was 22.1% (95% CI: 7.3-36.9%). Two deaths were caused by progression of AD. The probability of survival at 2 years was 70%. No single factor predicting the outcome could be identified. The retrospective nature of this study and the heterogeneous, partly incomplete data are its limitations. However, allogeneic HSCT can induce remission in patients suffering from refractory AD. These data provide the basis for carefully conducted prospective trials. Bone Marrow Transplantation (2009) 44, 27-33; doi:10.1038/bmt.2008.424; published online 12 January 2009
引用
收藏
页码:27 / 33
页数:7
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