Table 2

Patient characteristics and outcomes in the discovery (n = 110) and validation (n = 94) cohorts: validation cohort

1-y overall survival1-y relapse
nProbability (%)HR (95%CI) (risk of death)Cumulative incidence (%)HR (95%CI) (risk of relapse)
Age*  P = .09  P = .35  
 ≤40 y 44 55.0 21.1 
 >40 y 50 31.1 1.27 (0.72-1.90) 25.5 1.02 (0.45-2.30) 
Sex  P = .61  P = .19  
 Male 54 40.0 19.5 
 Female 40 43.7 0.78 (.45-1.37) 27.3 1.67 (0.77-3.61) 
Diagnosis  P = .51  P = .23  
 AML 39 43.6 33.3 
 Acute lymphoblastic leukemia 25 40.0 0.96 (0.50-18.5) 40.1 1.27 (0.53-2.78) 
 Myelodysplastic syndromes 80.0 0.26 (0.21-1.81) 20.0 0.55 (0.07-4.20) 
 Lymphoproliferative disorder 16 37.5 1.19 (0.57-2.53) 16.2 0.14 (0.2-1.18) 
 Chronic myeloid leukemia 56.6 0.62 (.21-1.81) 12.5 0.30 (0.04-2.32) 
Disease status at transplant  P = .04  P = .02  
 Complete remission 52 48.9 17.8 
 Refractory/relapsed disease 42 34.2 1.47 (1.09-2.56) 33.2 1.84 (1.13-4.22) 
Conditioning regimen  P = .87  P = .65  
 Myeloablative 73 40.9 25.1 
 Nonmyeloablative 21 47.4 1.09 (0.63-1.71) 17.6 0.85 (0.42-1.88) 
Graft  P = .73  P = .73  
 Double cord 88 40.5 31.9 
 Single cord 66.7 0.91 (0.50-1.68) 16.7 0.84 (0.23-1.86) 
CMV status  P = .78  P = .44  
 Seronegative 16 42.9 43.2 
 Seropositive 76 42.3 0.99 (0.77-1.36) 29.1 0.65 (0.20-1.91) 
HLA match between recipient and dominant CB unit§  P = .11  P = .26  
 7-8/8 10 75.1 20.1 
 5-6/8 31 36.8 1.61 (0.96-4.71) 36.8 1.4 (0.84-2.33) 
 ≤4/8 43 38.2 1.79 (0.91-3.54) 18.6 0.99 (0.70-1.24) 
Total mononuclear cells infused||  P = .91  P = .73  
 ≤3.8 × 108/kg 42.9 26.8 
 >3.8 × 108/kg 39.0 0.97 (0.55-1.70) 24.4 0.862 (0.37-2.03) 
Patient HLA C group,#  P = .002  P < .001  
C1/C1 38 50.0 22.2 
C1/C2 40 52.0 0.91 (0.47-1.76) 18.1 0.83 (0.30-2.34) 
C2/C2 16 12.5 2.73 (1.30-5.75) 68.7 5.34 (1.96-14.50) 
Patient HLA C group  P < .001  P < .001  
C1/x 78 51.3 19.5 
C2/C2 16 12.5 2.90 (1.56-5.38) 68.7 5.98 (2.73-13.10) 
Patients receiving CB grafts with the combined HLA-C1-KIR2DL2/L3/S2 genotype  P = .07  P = .05  
 Yes 37 56.8 16.2 
 No 57 36.8 1.70 (0.94-3.07) 35.7 2.38 (0.96-5.94) 
HLA-C1/x patients receiving CB grafts with the combined HLA-C1-KIR2DL2/L3/S2 genotype  P = .02  P = .01  
 Yes 31 67.7 6.5 
 No 47 40.4 2.33 (1.13-4.81) 28.3 5.02 (1.13-22.26) 
HLA match between recipient and dominant CB unit§  P = .11  P = .26  
 7-8/8 10 75.1 20.1 
 5-6/8 31 36.8 1.61 (0.96-4.71) 36.8 1.4 (0.84-2.33) 
 ≤4/8 43 38.2 1.79 (0.91-3.54) 18.6 0.99 (0.70-1.24) 
Patients received CB grafts with the combined HLA-C2-KIR2DL1/S1 genotype  P = .54  P = .20  
 Yes 35 46.6 23.1 
 No 59 41.7 1.19 (0.68-2.07) 34.1 1.31 (0.76-2.01) 
1-y overall survival1-y relapse
nProbability (%)HR (95%CI) (risk of death)Cumulative incidence (%)HR (95%CI) (risk of relapse)
Age*  P = .09  P = .35  
 ≤40 y 44 55.0 21.1 
 >40 y 50 31.1 1.27 (0.72-1.90) 25.5 1.02 (0.45-2.30) 
Sex  P = .61  P = .19  
 Male 54 40.0 19.5 
 Female 40 43.7 0.78 (.45-1.37) 27.3 1.67 (0.77-3.61) 
Diagnosis  P = .51  P = .23  
 AML 39 43.6 33.3 
 Acute lymphoblastic leukemia 25 40.0 0.96 (0.50-18.5) 40.1 1.27 (0.53-2.78) 
 Myelodysplastic syndromes 80.0 0.26 (0.21-1.81) 20.0 0.55 (0.07-4.20) 
 Lymphoproliferative disorder 16 37.5 1.19 (0.57-2.53) 16.2 0.14 (0.2-1.18) 
 Chronic myeloid leukemia 56.6 0.62 (.21-1.81) 12.5 0.30 (0.04-2.32) 
Disease status at transplant  P = .04  P = .02  
 Complete remission 52 48.9 17.8 
 Refractory/relapsed disease 42 34.2 1.47 (1.09-2.56) 33.2 1.84 (1.13-4.22) 
Conditioning regimen  P = .87  P = .65  
 Myeloablative 73 40.9 25.1 
 Nonmyeloablative 21 47.4 1.09 (0.63-1.71) 17.6 0.85 (0.42-1.88) 
Graft  P = .73  P = .73  
 Double cord 88 40.5 31.9 
 Single cord 66.7 0.91 (0.50-1.68) 16.7 0.84 (0.23-1.86) 
CMV status  P = .78  P = .44  
 Seronegative 16 42.9 43.2 
 Seropositive 76 42.3 0.99 (0.77-1.36) 29.1 0.65 (0.20-1.91) 
HLA match between recipient and dominant CB unit§  P = .11  P = .26  
 7-8/8 10 75.1 20.1 
 5-6/8 31 36.8 1.61 (0.96-4.71) 36.8 1.4 (0.84-2.33) 
 ≤4/8 43 38.2 1.79 (0.91-3.54) 18.6 0.99 (0.70-1.24) 
Total mononuclear cells infused||  P = .91  P = .73  
 ≤3.8 × 108/kg 42.9 26.8 
 >3.8 × 108/kg 39.0 0.97 (0.55-1.70) 24.4 0.862 (0.37-2.03) 
Patient HLA C group,#  P = .002  P < .001  
C1/C1 38 50.0 22.2 
C1/C2 40 52.0 0.91 (0.47-1.76) 18.1 0.83 (0.30-2.34) 
C2/C2 16 12.5 2.73 (1.30-5.75) 68.7 5.34 (1.96-14.50) 
Patient HLA C group  P < .001  P < .001  
C1/x 78 51.3 19.5 
C2/C2 16 12.5 2.90 (1.56-5.38) 68.7 5.98 (2.73-13.10) 
Patients receiving CB grafts with the combined HLA-C1-KIR2DL2/L3/S2 genotype  P = .07  P = .05  
 Yes 37 56.8 16.2 
 No 57 36.8 1.70 (0.94-3.07) 35.7 2.38 (0.96-5.94) 
HLA-C1/x patients receiving CB grafts with the combined HLA-C1-KIR2DL2/L3/S2 genotype  P = .02  P = .01  
 Yes 31 67.7 6.5 
 No 47 40.4 2.33 (1.13-4.81) 28.3 5.02 (1.13-22.26) 
HLA match between recipient and dominant CB unit§  P = .11  P = .26  
 7-8/8 10 75.1 20.1 
 5-6/8 31 36.8 1.61 (0.96-4.71) 36.8 1.4 (0.84-2.33) 
 ≤4/8 43 38.2 1.79 (0.91-3.54) 18.6 0.99 (0.70-1.24) 
Patients received CB grafts with the combined HLA-C2-KIR2DL1/S1 genotype  P = .54  P = .20  
 Yes 35 46.6 23.1 
 No 59 41.7 1.19 (0.68-2.07) 34.1 1.31 (0.76-2.01) 
*

Median age was 41.0 y (range, 1-73).

Five patients had chronic lymphocytic leukemia; 5 patients had Hodgkin disease, and 6 patients had non-Hodgkin lymphoma.

Two patients had missing data.

§

The identity of the dominant CB unit could not be ascertained in 10 cases.

||

The median value for the total of nucleated cells infused was 3.8 × 108/kg (range, 1.5 × 108/kg to 34.2 × 108/kg).

The P values for the comparisons of outcomes in C1/C1 vs C2/C2 patients were P = .007 for OS and P < .001 for cumulative incidence of progression.

#

The P values for the comparisons of outcomes in C1/C2 vs C2/C2 patients were P = .001 for OS and P < .001 for cumulative incidence of progression.

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