Table 2

Results of multivariate Cox regression analyses of OS and EFS in the test cohort

VariableOverall survival (n = 78)*
Event-free survival (n = 77)
HR (95% CI)PHR (95% CI)P
Age 1.43 (1.10-1.87) .009 1.34 (1.07-1.69) .011 
NPM1 mutation 0.54 (0.29-1.02) .06 0.41 (0.23-0.73) .002 
FLT3 ITD§ 
    Low FLT3 ITD/wt ratio 1.38 (0.64-2.97) .41 1.12 (0.55-2.27) .74 
    High FLT3 ITD/wt ratio 1.26 (0.42-3.82) .61 1.52 (0.51-4.54) .45 
Microarray-based continuous risk score 1.64 (1.07-2.54) .037 1.68 (1.07-2.64) .024 
VariableOverall survival (n = 78)*
Event-free survival (n = 77)
HR (95% CI)PHR (95% CI)P
Age 1.43 (1.10-1.87) .009 1.34 (1.07-1.69) .011 
NPM1 mutation 0.54 (0.29-1.02) .06 0.41 (0.23-0.73) .002 
FLT3 ITD§ 
    Low FLT3 ITD/wt ratio 1.38 (0.64-2.97) .41 1.12 (0.55-2.27) .74 
    High FLT3 ITD/wt ratio 1.26 (0.42-3.82) .61 1.52 (0.51-4.54) .45 
Microarray-based continuous risk score 1.64 (1.07-2.54) .037 1.68 (1.07-2.64) .024 
*

One patient was not included because of missing data on FLT3 ITD/wt allelic ratio.

Data on EFS were available for 77 of the 79 patients in the test dataset.

The hazard ratio is given for an age difference of 10 years.

§

Hazard ratios are for the comparison with patients without detectable FLT3 ITD (ie, a FLT3 ITD/wt allelic ratio of 0).

The hazard ratio is given for a change of the score equal to its interquartile range.

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