Table 5.

Univariate analysis

Risk factorEnd points
RFS, 3 yRelapse, 3 yNRM (d 100/3 y)
  Probability/Cumulative incidence (%)/HR (CI)  
Donor     
 HLA-identical related  56 16 12/28 
 Unrelated  59 11 13/30  
 HLA ≠  27 21 36/52 
 P .11 .57 .11  
FAB classification     
 RA/RARS  65 5/1.05-151 15/30 
 RAEB  32 34/8.5 (2.2-33) 21/30 
 RAEB-T/tAML  18 32/8.6 (1.7-43) 10/51 
 Other  67 0/NC5-152 17/33 
 P .08 .002 .86 
Cytogenetic risk     
 Good  60 9/1.05-151 14/31 
 Intermediate  56 13/2.1 (0.4-11) 13/31  
 Poor  40 26/5.2 (1.5-18) 21/34 
 P .11 .03 .75 
Etiology     
 De novo  62/1.05-151 11/1.05-151 13/27 
 Chemo/radiotherapy  12/2.8 (1.4-5.7) 41/5.4 (1.7-17) 29/48 
 Predisposing disease  50/1.3 (0.6-2.9) 6/0.8 (0.1-6.4) 18/44 
 P .03 .03 .32  
IPSS risk     
 Low  80 0/NC5-152 13/20 
 Intermediate-1  64 6/0.2 (0.0-0.6) 9/30 
 Intermediate-2  40 29/0.7 (0.2-2.7) 25/31 
 High  29 42/1.05-151 0/29 
 P .14 .009 .83 
Acute GVHD     
 Grades 0-I  60 19 10/20 
 Grades II-IV  51 12 18/37 
 P .05 .56 .006 
Risk factorEnd points
RFS, 3 yRelapse, 3 yNRM (d 100/3 y)
  Probability/Cumulative incidence (%)/HR (CI)  
Donor     
 HLA-identical related  56 16 12/28 
 Unrelated  59 11 13/30  
 HLA ≠  27 21 36/52 
 P .11 .57 .11  
FAB classification     
 RA/RARS  65 5/1.05-151 15/30 
 RAEB  32 34/8.5 (2.2-33) 21/30 
 RAEB-T/tAML  18 32/8.6 (1.7-43) 10/51 
 Other  67 0/NC5-152 17/33 
 P .08 .002 .86 
Cytogenetic risk     
 Good  60 9/1.05-151 14/31 
 Intermediate  56 13/2.1 (0.4-11) 13/31  
 Poor  40 26/5.2 (1.5-18) 21/34 
 P .11 .03 .75 
Etiology     
 De novo  62/1.05-151 11/1.05-151 13/27 
 Chemo/radiotherapy  12/2.8 (1.4-5.7) 41/5.4 (1.7-17) 29/48 
 Predisposing disease  50/1.3 (0.6-2.9) 6/0.8 (0.1-6.4) 18/44 
 P .03 .03 .32  
IPSS risk     
 Low  80 0/NC5-152 13/20 
 Intermediate-1  64 6/0.2 (0.0-0.6) 9/30 
 Intermediate-2  40 29/0.7 (0.2-2.7) 25/31 
 High  29 42/1.05-151 0/29 
 P .14 .009 .83 
Acute GVHD     
 Grades 0-I  60 19 10/20 
 Grades II-IV  51 12 18/37 
 P .05 .56 .006 

Other factors considered included donor and patient CMV serology, patient age, donor age, disease duration (≤ 6 mo; 6-12 mo; 12-24 mo; > 24 mo), busulfan levels (< 800; 800-900; > 900 ng/mL), donor/patient gender combination, source of hemopoietic stem cells (marrow versus PBSCs), cell dose. None of these was significant for any end point.

F5-151

Reference for calculation of hazard ratio (HR).

F5-152

Cannot be computed.

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