Table 2

Multivariate analyses for CXXC5 expression

Variable*OR/HR95% CIP
Relapse rate 
 Low CXXC5 0.5 0.3-0.8 .007 
 Cytogenetic risk 1.9 1.2-2.9 .005 
 WBC 1.06 1.0-1.1 .005 
CEBPA mut., biallelic 0.4 0.2-1.0 .05 
ASXL1 mut. 9.5 2.0-45 .004 
Overall survival    
 Low CXXC5 0.6 0.5-0.8 .001 
 Cytogenetic risk 1.7 1.3-2.1 <.001 
 Age 1.2 1.0-1.3 .004 
FLT3-ITD/NPM1 wt 1.7 1.2-2.5 .004 
NPM1 mut./FLT3-ITD neg. 0.6 0.4-0.8 .006 
CEBPA mut., biallelic 0.3 0.2-0.6 <.001 
DNMT3A mut. 1.4 1.1-2.0 .02 
ASXL1 mut. 1.6 1.0-2.5 .04 
Event-free survival 
 Low CXXC5 0.6 0.5-0.8 <.001 
 Cytogenetic risk 1.6 1.3-2.0 <.001 
 WBC 1.02 1.0-1.0 .04 
FLT3-ITD/NPM1 wt 1.7 1.2-2.5 .006 
NPM1 mut./FLT3-ITD neg. 0.6 0.4-0.9 .009 
CEBPA mut., biallelic 0.3 0.2-0.6 <.001 
DNMT3A mut. 1.4 1.0-1.8 .04 
ASXL1 mut. 2.0 1.2-3.2 .005 
Variable*OR/HR95% CIP
Relapse rate 
 Low CXXC5 0.5 0.3-0.8 .007 
 Cytogenetic risk 1.9 1.2-2.9 .005 
 WBC 1.06 1.0-1.1 .005 
CEBPA mut., biallelic 0.4 0.2-1.0 .05 
ASXL1 mut. 9.5 2.0-45 .004 
Overall survival    
 Low CXXC5 0.6 0.5-0.8 .001 
 Cytogenetic risk 1.7 1.3-2.1 <.001 
 Age 1.2 1.0-1.3 .004 
FLT3-ITD/NPM1 wt 1.7 1.2-2.5 .004 
NPM1 mut./FLT3-ITD neg. 0.6 0.4-0.8 .006 
CEBPA mut., biallelic 0.3 0.2-0.6 <.001 
DNMT3A mut. 1.4 1.1-2.0 .02 
ASXL1 mut. 1.6 1.0-2.5 .04 
Event-free survival 
 Low CXXC5 0.6 0.5-0.8 <.001 
 Cytogenetic risk 1.6 1.3-2.0 <.001 
 WBC 1.02 1.0-1.0 .04 
FLT3-ITD/NPM1 wt 1.7 1.2-2.5 .006 
NPM1 mut./FLT3-ITD neg. 0.6 0.4-0.9 .009 
CEBPA mut., biallelic 0.3 0.2-0.6 <.001 
DNMT3A mut. 1.4 1.0-1.8 .04 
ASXL1 mut. 2.0 1.2-3.2 .005 

CI, confidence interval; HR, hazard ratio; mut., mutated; neg., negative; OR, odds ratio; WBC, white blood cell count; wt, wild-type.

*

Variables considered for model inclusion were (see supplemental Material for details): CXXC5 expression (below vs above median level), cytogenetic risk groups (good, intermediate, unfavorable), age (10-year increase), WBC (10/nl increase), FLT3-ITD34 /NPM1 wild-type (present vs absent), NPM1 mutation35 /FLT3-ITD negative (present vs absent), CEBPA biallelic mutation36  (present vs absent), DNMT3A mutation37  (present vs absent), ASXL1 mutation38  (present vs absent), WT1 mutation (present vs absent), WT1 expression (lower vs higher than median).

Below median expression level.

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