ATG as part of the conditioning regimen reduces transplant-related mortality (TRM) and improves overall survival after unrelated stem cell transplantation in patients with chronic myelogenous leukemia (CML)

被引:46
作者
Zander, AR
Kröger, N
Schleuning, M
Finke, J
Zabelina, T
Beelen, D
Schwerdtfeger, R
Baurmann, H
Bornhäuser, M
Ehninger, G
Fauser, AA
Kiehl, M
Trenschel, R
Ottinger, HD
Bertz, H
Berger, J
Kolb, HJ
Schaefer, UW
机构
[1] Univ Hamburg, Hosp Eppendorf, Dept Bone Marrow Transplantat, D-20246 Hamburg, Germany
[2] Univ Hosp Munchen, Dept Bone Marrow Transplantat, Munich, Germany
[3] Univ Hosp Freiburg, Dept Med, Freiburg, Germany
[4] Univ Hosp Essen, Dept Bone Marrow Transplantat, Essen, Germany
[5] German Clin Diagnost, Ctr Bone Marrow Transplantat, Wiesbaden, Germany
[6] Univ Hosp Dresden, Med Clin 1, Dresden, Germany
[7] Clin Bone Marrow Transplantat, Idar Oberstein, Germany
[8] Univ Hamburg, Hosp Eppendorf, Dept Math Med, D-20246 Hamburg, Germany
关键词
GvHD; ATG; MuD=mismatched unrelated donor transplantation;
D O I
10.1038/sj.bmt.1704157
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Matched unrelated donor transplants have an increased risk of severe graft-versus-host disease and transplant-related mortality (TRM). ATG has been introduced to decrease GvHD and to facilitate engraftment. We conducted a retrospective analysis of 333 patients with chronic myelogenous leukemia, who were treated with Fresenius ATG (n = 145, average =90 mg/kg bw, range 40-90 mg/kg bw) or standard immunosuppression without ATG (n = 188). Both groups were comparable regarding distribution of age, sex, HLA-matched vs mismatched donors. ATG Fresenius led to a faster leukocyte engraftment, decreased the incidence of acute GvHD and TRM (P = 0.01 and P = 0.03) and led to a significant better overall survival (70 vs 57%, P = 0.03). We concluded that a prospective randomized study is needed to evaluate the definite role of ATG in hemopoietic stem cell transplantation.
引用
收藏
页码:355 / 361
页数:7
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