Skip to main content
. Author manuscript; available in PMC: 2018 Aug 25.
Published in final edited form as: Leukemia. 2018 Feb 25;32(6):1338–1348. doi: 10.1038/s41375-018-0068-2

Table 2.

Multivariable outcome analyses of older patients with de novo acute myeloid leukemia

Variables in final model Complete remission Disease-free survival Overall survival
OR (95% CI) P-valuea HR (95% CI) P-valuea HR (95% CI) P-valuea
NPM1, mutated vs wild-type 3.46 (2.01–5.97) <0.001 0.60 (0.45–0.81) <0.001 0.55 (0.44–0.69) <0.001
U2AF1, mutated vs wild-type 0.40 (0.18–0.90) 0.03
WT1, mutated vs wild-type 0.22 (0.07–0.71) 0.01
Normal karyotype, present vs absent mutated v wild-type 1.70 (1.06–2.74) 0.03
SF1, mutated vs wild-type
FLT3-ITD, present vs absent 2.30 (1.62–3.26) <0.001 1.85 (1.43–2.39) <0.001
WBC, per 50-unit increase 1.22 (1.06–1.41) 0.007
Complex karyotype,b present vs absent 4.21 (2.45–7.21) <0.001 1.78 (1.24–2.55) 0.002
BCOR, mutated vs wild-type 1.82 (1.23–2.69) 0.003
TP53, mutated vs wild-type 1.91 (1.25–2.93) 0.003
t(9;11), present vs absent 2.19 (1.07–4.47) 0.03

Abbreviations: CI, confidence interval; FLT3-ITD, internal tandem duplication of the FLT3 gene; HR, hazard ratio; OR, odds ratio; WBC, white blood cell count.

An OR <1 (>1) means lower (higher) CR rate for first category listed of a dichotomous variable or higher values of a continuous variable. A HR >1 (<1) corresponds to a higher (lower) risk for first category listed of a dichotomous variable or higher values of a continuous variable. A limited backward selection technique was used to build the final model for achievement of complete remission, disease-free and overall survival. Variables considered in the model were variables that were significant at the likelihood ratio test P-value <.20 from the univariable models (detailed in the Supplementary Information).

a

P-values for CR were determined by logistic regression. P-values for DFS and OS were determined using Cox proportional hazards regression.

b

Complex karyotype is defined by the presence of ≥3 chromosome aberrations.