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. 2016 May 31;128(2):297–312. doi: 10.1182/blood-2016-03-706317

Table 1.

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

1-y overall survival 1-y relapse rate
n Probability (%) HR (95%CI) (risk of death) Cumulative incidence (%) HR (95%CI) (risk of relapse)
Age* P = .08 P = .74
 ≤40 y 59 52.4 1 32.7 1
 >40 y 51 35.6 1.57 (0.94-2.63) 36.0 1.12 (0.56-2.22)
Sex P = .23 P = .24
 Male 48 40.6 1 40.5 1
 Female 62 47.9 0.73 (0.44-1.22) 35.1 0.66 (0.23-1.61)
Diagnosis P = .75 P = .40
 AML 44 41.5 1 41.0 1
 Acute lymphoblastic leukemia 24 41.7 0.95 (0.49-1.84) 23.1 0.51 (0.18-1.38)
 Myelodysplastic syndromes 19 40.6 1.00 (0.49-2.0) 47.6 1.06 (0.45-2.48)
 Lymphoproliferative disorderI 22 43.3 0.75 (0.28-1.51) 30.3 0.44 (0.13-1.50)
 Chronic myeloid leukemia 1 100.0 0.0
Disease status at transplant P = .06 P = .006
 Complete remission 67 52.9 1 23.2 1
 Refractory/relapsed disease 43 31.9 1.63 (0.97-2.73) 51.3 2.55 (1.27-5.10)
Conditioning regimen P = .20 P = .55
 Myeloablative 79 38.1 1 46.3 1
 Nonmyeloablative 31 22.1 1.19 (0.67-2.09) 40.9 0.56 (0.23-1.36)
Graft P = .22 P = .20
 Double cord 105 45.9 1 32.6 1
 Single cord 5 20.0 1.36 (0.82-2.27) 0.60 1.51 (0.84-2.74)
CMV status P = .84 P = .43
 Seronegative 11 53.0 1 56.2 1
 Seropositive 97 43.6 1.10 (0.44-2.75) 32.0 0.66 (0.23-1.89)
HLA match between recipient and dominant CB unit§ P = .50 P = .34
 7-8/8 16 61.4 1 25.1 1
 5-6/8 46 47.1 1.41 (0.48-4.13) 30.1 1.33 (0.42-6.01)
 ≤4/8 38 40.8 1.80 (0.61-5.27) 39.6 1.60 (0.61-4.81)
Total mononuclear cells infused|| P = .90 P = .99
 ≤4.1 × 108/kg 56 46.1 1 34.2 1
 >4.1 × 108/kg 54 42.6 1.035 (0.62-1.73) 33.5 0.99 (0.50-1.96)
Patient HLA C group P < .001 P < .001
C1/C1 31 59.9 1 27.3 1
C1/C2 55 48.7 1.35 (0.68-2.67) 24.9 0.92 (0.38-2.26)
C2/C2 24 15.0 4.33 (2.10-8.94) 67.8 4.05 (1.66-9.87)
Patient HLA C group P < .001 P < .001
C1/x 86 52.9 1 26.0 1
C2/C2 24 15.0 3.56 (2.05-6.18) 67.8 4.25 (2.09-8.63)
Patients receiving CB grafts with the combined HLA-C1-KIR2DL2/L3/S2 genotype P = .002 P = .009
 Yes 67 64.6 1 46.9 1
 No 37 34.3 2.65 (1.39-5.03) 16.0 3.07 (1.26-7.47)
HLA-C1/x patients receiving CB grafts with the combined HLA-C1-KIR2DL2/L3/S2 genotype P = .003 P = .002
 Yes 31 74.2 1 6.7 1
 No 49 41.3 3.31 (1.45-7.50) 40.1 6.98 (1.61-30.25)
Patients receiving CB grafts with the combined HLA-C2-KIR2DL1/S1 genotype P = .17 P = .72
 Yes 47 51.9 1 35.2 1
 No 57 39.1 1.45 (0.85-2.49) 34.0 1.13 (0.56-2.27)
Number of CB units with haplotype B P = .45 P = .30
 2 CB units 88 44.9 1 31.2 1
 1 CB units 14 42.9 0.961 (0.45-2.03) 43.6 1.37 (0.18-10.15)
 0 CB units 2 50.0 1.12 (0.09-16.27) 50.0 2.12 (0.91-4.93)
*

The median age was 38 y (range, 2-73).

Six patients had Hodgkin disease; 4 had chronic lymphocytic leukemia, and 12 had non-Hodgkin lymphoma.

Two patients had missing data.

§

The identity of the dominant CB unit could not be ascertained in 14 cases.

||

The median value for the total nucleated cells infused was 4.1 × 108/kg (range, 2.0 × 108/kg to 19.5 × 108/kg).

Six patients had missing data.