Table 1.

Four-year cumulative incidence of progression to AML and 4-year probability of PFS and OS according to patient characteristics

VariablenUnivariate analysis 4-y probabilityMultivariate analysis RR (95% CI)
AMLPFSOSAMLPFSOS
Age, y*  P = .34 P = .03 P = .02   P = .02 
 ≤70 53 27.2 55.8 57.0   
 >70 55 17.6 28.0 28.7   1.97 (1.08-3.59) 
Sex  P = .79 P = .71 P = .91    
 Female 34 20.3 44.2 43.6    
 Male 74 23.6 41.7 43.6    
WHO type  P = .07 P = .01 P = .01    
 RA 11 29.3 60.6 60.0    
 RARS 0.0 85.7 85.7    
 RCMD 35 11.9 44.9 47.5    
 RCMD-RS 20.0 60.0 60.0    
 RAEB-1 25 42.6 21.4 23.2    
 RAEB-2 18 36.7 13.8 13.8    
 MDS-U 0.0 100.0 100.0    
 del(5q) 0.0 100.0 100.0    
WHO type  P = .07 P < .001 P < .001    
 RAEB-1 and 2 43 36.3 18.5 18.7 
 Others 65 13.0 59.8 61.0 
IPSS  P = .003 P < .001 P < .001  P = .01 P = .01 
 Low 48 5.6 71.3 74.0 
 Intermediate-1 22 34.2 39.5 38.4 2.34 (0.97-5.58) 2.35 (0.95-5.80) 
 Intermediate-2 10 22.2 22.2 22.2 5.08 (1.67-15.42) 4.39 (1.48-13.01) 
 High 28 40.9 4.3 4.8 6.10 (2.01-18.52) 5.74 (1.94-17.04) 
Cytogenetic risk group  P = .001 P < .001 P < .001 P = .003 P = .03 P = .004 
 Low 69 12.1 62.6 63.9 
 Intermediate 14 30.8 15.9 11.9 2.87 (0.84-9.83) 3.76 (1.48-9.54) 5.46 (2.09-14.27) 
 High 25 47.3 4.8 5.7 5.29 (2.01-13.95) 2.07 (0.75-5.72) 2.40 (0.90-6.40) 
No. of activating KIR genes  P = .87 P = .06 P = .09    
 0-1 65 22.7 36.7 39.2 
 ≥2 43 22.6 52.5 51.3 
Activating KIR gene haplotype  P = .02 P = .02 P = .10 P = .02 P = .001 P = .02 
 Haplotype B 80 16.8 48.9 48.2 
 Haplotype A 28 37.1 27.3 31.2 2.67 (1.13-6.31) 2.96 (1.59-5.52) 2.25 (1.17-4.31) 
HLA-C group  P = .50 P = .78 P = .90    
 HLA-C1/x§ 93 24.4 44.2 44.4 
 HLA-C2/2 13 15.4 35.2 39.6 
VariablenUnivariate analysis 4-y probabilityMultivariate analysis RR (95% CI)
AMLPFSOSAMLPFSOS
Age, y*  P = .34 P = .03 P = .02   P = .02 
 ≤70 53 27.2 55.8 57.0   
 >70 55 17.6 28.0 28.7   1.97 (1.08-3.59) 
Sex  P = .79 P = .71 P = .91    
 Female 34 20.3 44.2 43.6    
 Male 74 23.6 41.7 43.6    
WHO type  P = .07 P = .01 P = .01    
 RA 11 29.3 60.6 60.0    
 RARS 0.0 85.7 85.7    
 RCMD 35 11.9 44.9 47.5    
 RCMD-RS 20.0 60.0 60.0    
 RAEB-1 25 42.6 21.4 23.2    
 RAEB-2 18 36.7 13.8 13.8    
 MDS-U 0.0 100.0 100.0    
 del(5q) 0.0 100.0 100.0    
WHO type  P = .07 P < .001 P < .001    
 RAEB-1 and 2 43 36.3 18.5 18.7 
 Others 65 13.0 59.8 61.0 
IPSS  P = .003 P < .001 P < .001  P = .01 P = .01 
 Low 48 5.6 71.3 74.0 
 Intermediate-1 22 34.2 39.5 38.4 2.34 (0.97-5.58) 2.35 (0.95-5.80) 
 Intermediate-2 10 22.2 22.2 22.2 5.08 (1.67-15.42) 4.39 (1.48-13.01) 
 High 28 40.9 4.3 4.8 6.10 (2.01-18.52) 5.74 (1.94-17.04) 
Cytogenetic risk group  P = .001 P < .001 P < .001 P = .003 P = .03 P = .004 
 Low 69 12.1 62.6 63.9 
 Intermediate 14 30.8 15.9 11.9 2.87 (0.84-9.83) 3.76 (1.48-9.54) 5.46 (2.09-14.27) 
 High 25 47.3 4.8 5.7 5.29 (2.01-13.95) 2.07 (0.75-5.72) 2.40 (0.90-6.40) 
No. of activating KIR genes  P = .87 P = .06 P = .09    
 0-1 65 22.7 36.7 39.2 
 ≥2 43 22.6 52.5 51.3 
Activating KIR gene haplotype  P = .02 P = .02 P = .10 P = .02 P = .001 P = .02 
 Haplotype B 80 16.8 48.9 48.2 
 Haplotype A 28 37.1 27.3 31.2 2.67 (1.13-6.31) 2.96 (1.59-5.52) 2.25 (1.17-4.31) 
HLA-C group  P = .50 P = .78 P = .90    
 HLA-C1/x§ 93 24.4 44.2 44.4 
 HLA-C2/2 13 15.4 35.2 39.6 

MDS-U, MDS unclassified; RA, refractory anemia; RAEB, refractory anemia with excess blasts; RARS, refractory anemia with ring sideroblasts; RCMD, refractory cytopenia with multilineage dysplasia; RCMD-RS, refractory cytopenia with multilineage dysplasia and ringed sideroblasts.

*

The median age was 68.4 years (range, 18.1-88.4 years).

Two patients had missing data.

Includes HLA-C1/C1 and HLA-C1/C2.

§

Haplotype B patients were further characterized as haplotype B centromeric and telomeric according to KIR gene content. They had similar outcomes, namely progression to AML (17.0% vs 16.0%; P = .96); PFS (45.2% vs 37.1%; P = .78); OS (45.8% vs 57.5%; P = .82).

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