G-CSF given after haematopoietic stem cell transplantation using HLA-identical sibling donors is associated to a higher incidence of acute GVHD II-IV

被引:63
作者
Remberger, M
Naseh, N
Aschan, J
Barkholt, L
LeBlanc, K
Svennberg, P
Ringdén, O
机构
[1] Huddinge Univ Hosp, Ctr Allogen Stem Cell Transplantat, SE-14186 Stockholm, Sweden
[2] Huddinge Univ Hosp, Dept Clin Immunol, SE-14186 Stockholm, Sweden
[3] Huddinge Univ Hosp, Dept Haematol, SE-14186 Stockholm, Sweden
关键词
HSCT; G-CSF; GVHD; TRM;
D O I
10.1038/sj.bmt.1704108
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The effect of granulocyte colony-stimulating factor (G-CSF), given after transplantation, was studied in 155 patients transplanted with haematopoietic stem cells (HSCT) from HLA-identical sibling donors at Huddinge University Hospital between 1993 and 2001. Only patients with haematological malignancies were included. Conditioning consisted of total-body irradiation in 118 and busulphan in 37 patients. They were all given methotrexate combined with cyclosporine as graft-versus-host disease (GVHD) prophylaxis. Of the 155 patients, 66 (43%) received G-CSF after HSCT. Those given G-CSF had a significantly short er time to neutrophil engraftment (P<0.001). G-CSF treatment had no effect on erythrocyte transfusions, platelet engraftment and infections. However, patients treated with G-CSF had a significantly higher incidence of grades II-IV acute GVHD than those not given this treatment (34 vs 9%, P<0.001). The multivariate analysis showed that the effect of G-CSF was independent of other known risk factors for grades II-IV acute GVHD. Death from GVHD occurred in four and two cases (P=0.06) in the two groups, respectively. The cumulative incidences of transplant-related mortality, survival, chronic GVHD, relapse and relapse-free survival were similar in both groups. In conclusion, G-CSF given after HLA-identical sibling HSCT was associated with a higher risk of grades II-IV acute GVHD, but not transplant-related mortality.
引用
收藏
页码:217 / 223
页数:7
相关论文
共 48 条
[1]   ALLOGENEIC MARROW TRANSPLANTATION AND THE USE OF HEMATOPOIETIC GROWTH-FACTORS [J].
APPELBAUM, FR .
STEM CELLS, 1995, 13 (04) :344-350
[2]  
ASCHAN J, 1994, BONE MARROW TRANSPL, V14, P79
[3]  
ASCHAN J, 1994, BONE MARROW TRANSPL, V14, P601
[4]   Influence of recombinant human granulocyte colony-stimulating factor (filgrastim) on hematopoietic recovery and outcome following allogeneic bone marrow transplantation (BMT) from volunteer unrelated donors [J].
Berger, C ;
Bertz, H ;
Schmoor, C ;
Behringer, D ;
Potthoff, K ;
Mertelsmann, R ;
Finke, J .
BONE MARROW TRANSPLANTATION, 1999, 23 (10) :983-990
[5]   A randomized, double-blind trial of filgrastim (granulocyte colony-stimulating factor) versus placebo following allogeneic blood stem cell transplantation [J].
Bishop, MR ;
Tarantolo, SR ;
Geller, RB ;
Lynch, JC ;
Bierman, PJ ;
Pavletic, ZS ;
Vose, JM ;
Kruse, S ;
Dix, SP ;
Morris, ME ;
Armitage, JO ;
Kessinger, A .
BLOOD, 2000, 96 (01) :80-85
[6]   Low-dose cyclosporine of short duration increases the risk of mild and moderate GVHD and reduces the risk of relapse in HLA-identical sibling marrow transplant recipients with leukaemia [J].
Carlens, S ;
Aschan, J ;
Remberger, M ;
Dilber, MS ;
Ringdén, O .
BONE MARROW TRANSPLANTATION, 1999, 24 (06) :629-635
[7]  
Carlens S, 1998, CLIN TRANSPLANT, V12, P84
[8]  
FERRARA JLM, 1991, NEW ENGL J MED, V324, P667
[9]   The immunopathophysiology of acute graft-versus-host disease [J].
Ferrara, JLM ;
Cooke, KR ;
Pan, LY ;
Krenger, W .
STEM CELLS, 1996, 14 (05) :473-489
[10]   CLINICAL MANIFESTATIONS OF GRAFT VERSUS HOST DISEASE IN HUMAN RECIPIENTS OF MARROW FROM HL-A-MATCHED SIBLING DONORS [J].
GLUCKSBERG, H ;
STORB, R ;
FEFER, A ;
BUCKNER, CD ;
NEIMAN, PE ;
CLIFT, RA ;
LERNER, KG ;
THOMAS, ED .
TRANSPLANTATION, 1974, 18 (04) :295-304