Table 1

Significant variables in multivariate analysis for OS and RFS

Endpoint/variableHR95% CIP
OS    
    Age: above vs below median 2.04 1.41-2.99 < .001 
    NPM1/FLT3 mutation status: low risk* vs high risk 0.66 0.44-0.97 .035 
    Platelets: above vs below median 0.61 0.42-0.88 .008 
    WT1 SNP rs16754 0.43 0.26-0.71 .001 
RFS    
    WT1 SNP rs16754 0.60 0.39-0.92 .019 
    NPM1 mutation 0.51 0.35-0.74 < .001 
    CEBPA mutation 0.36 0.19-0.67 .001 
Endpoint/variableHR95% CIP
OS    
    Age: above vs below median 2.04 1.41-2.99 < .001 
    NPM1/FLT3 mutation status: low risk* vs high risk 0.66 0.44-0.97 .035 
    Platelets: above vs below median 0.61 0.42-0.88 .008 
    WT1 SNP rs16754 0.43 0.26-0.71 .001 
RFS    
    WT1 SNP rs16754 0.60 0.39-0.92 .019 
    NPM1 mutation 0.51 0.35-0.74 < .001 
    CEBPA mutation 0.36 0.19-0.67 .001 

Variables with P values of less than or equal to .1 in univariate analysis were included for the multivariate analysis. For OS, these included age, FLT3-ITD, WT1 expression, extramedullary disease, platelets, NPM1/FLT3 status low risk vs others, CEBPA mutation, and WT1 SNP rs16754. For RFS, these included CEBPA mutation, WT1 SNP rs16754, NPM1 mutation, and NPM1/FLT3 status low risk vs others. Variables evaluated in univariate analysis (see also supplemental Table 3) included FLT3-ITD, age, WT1 expression, extramedullary disease, platelets high vs low, NPM1/FLT3 status low risk vs others, CEBPA mutation, WT1 SNP rs16754, NPM1 mutation, WT1 mutation, sibling vs no sibling donor, white blood cells high vs low, peripheral blasts high vs low, hemoglobin high vs low, de novo vs secondary AML, sex, IDH2 mutation, and IDH1 or IDH2 mutation combined.

HR indicates hazard ratio; and CI, confidence interval.

*

NPM1/FLT3 low risk is defined as the presence of an NPM1 mutation in the absence of an FLT3-ITD.

or Create an Account

Close Modal
Close Modal