Table 1.

Clinical details, graft composition, and outcomes in leukocyte antigen haplotype–mismatched transplant recipients receiving and not receiving granulocyte colony-stimulating factor (G-CSF) after transplantation

CharacteristicG-CSF*
(n = 43; 1995-1998)3
No G-CSF
(n = 36; 1999-2000)
Mean (range) age, y 22 (4-53) 30 (11-60) 
Disease   
 Acute myeloblastic leukemia 20 20 
 Acute lymphoblastic leukemia 23 16  
Status at transplantation   
 Poor-risk complete remission  7  7 
 Beyond second complete remission 21 15  
 Chemoresistant relapse 15 14  
Graft processing E-ros + Ceprate MACS  
Graft composition   
 Mean (range) CD34+ × 106/kg 10.8 (3.1-27.5) 12.1 (5.1-25.4)  
 Mean (range) CD3+ × 104/kg 2.0 (0.1-4.2) 1.1 (0.1-3)  
 Mean (range) percentage of CD14+cells 11.8 (0.8-51.8) < 2  
No. (%) of primary engraftments 41 (95.3) 34 (93)  
Neutrophils > 0.5 × 109/L (day after transplantation)  9 13 
Platelets > 50 × 109/L (day after transplantation) 18 17  
No. (%) of deaths during remission 15/43 (35) 9/36 (25) 
No. (%) of relapses 15/43 (35) 9/36 (25) 
No. (%) of cases of acute GVHD  0  4 
CharacteristicG-CSF*
(n = 43; 1995-1998)3
No G-CSF
(n = 36; 1999-2000)
Mean (range) age, y 22 (4-53) 30 (11-60) 
Disease   
 Acute myeloblastic leukemia 20 20 
 Acute lymphoblastic leukemia 23 16  
Status at transplantation   
 Poor-risk complete remission  7  7 
 Beyond second complete remission 21 15  
 Chemoresistant relapse 15 14  
Graft processing E-ros + Ceprate MACS  
Graft composition   
 Mean (range) CD34+ × 106/kg 10.8 (3.1-27.5) 12.1 (5.1-25.4)  
 Mean (range) CD3+ × 104/kg 2.0 (0.1-4.2) 1.1 (0.1-3)  
 Mean (range) percentage of CD14+cells 11.8 (0.8-51.8) < 2  
No. (%) of primary engraftments 41 (95.3) 34 (93)  
Neutrophils > 0.5 × 109/L (day after transplantation)  9 13 
Platelets > 50 × 109/L (day after transplantation) 18 17  
No. (%) of deaths during remission 15/43 (35) 9/36 (25) 
No. (%) of relapses 15/43 (35) 9/36 (25) 
No. (%) of cases of acute GVHD  0  4 

E-ros + Ceprate indicates sheep red blood cell rosetting plus positive selection of CD34+ cells with use of Ceprate SC columns; MACS, magnetically activated cell sorter; and GVHD, graft-versus-host disease.

*

G-CSF was given in a dosage of 5 μg/kg of body weight daily for the first 20 days after transplantation.

CD3+ T cells contained the same proportion (50%-70%) of CD4+ cells in the two series.

There were no significant differences between patients receiving G-CSF and those not receiving G-CSF (P = .34) as determined 270 days after transplantation.

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