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. Author manuscript; available in PMC: 2020 May 1.
Published in final edited form as: Clin Cancer Res. 2019 Aug 2;25(21):6524–6531. doi: 10.1158/1078-0432.CCR-19-0725

Table 2.

Multivariable analyses for disease-free survival and overall survival performed in younger (aged <60 years) patients with cytogenetically normal acute myeloid leukemia

Variables Disease-free survival (n=266) Overall survival (n=315)
P-value HR (95% CI) P-value HR (95% CI)
Age, continuous 0.005 1.20 (1.06–1.37)
DNMT3A, mut vs wt <0.001 1.94 (1.41–2.67) 0.003 1.58 (1.17–2.14)
FLT3-ITD, yes vs no <0.001 2.31 (1.67–3.19) <0.001 2.08 (1.55–2.80)
FLT3-TKD, mut vs wt 0.04 0.52 (0.28–0.97)
HG, continuous 0.02 0.91 (0.84–0.98)
RUNX1, mut vs wt 0.002 2.82 (1.44–5.52) <0.001 3.82 (2.17–6.75)
UPD of 11p, yes vs no 0.04 0.35 (0.13–0.98)
UPD of 13q, yes vs no 0.009 2.10 (1.20–3.67)
WT1, mut vs wt 0.03 1.70 (1.04–2.77) <0.001 2.62 (1.70–4.03)

Abbreviations: UPD, uniparental disomy; CI, confidence interval; HG, hemoglobin levels; HR, hazard ratio; FLT3-ITD, internal tandem duplication of the FLT3 gene; mut, mutated; n, number; FLT3-TKD, tyrosine kinase domain mutation in the FLT3 gene; wt, wild-type

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 models with variables that were significant at the likelihood ratio test P-value <0.20 from univariable models for each outcome. For DFS those variables were: HG, platelet count, white blood cell count, UPD of 11p, UPD of 13q, FLT3-ITD status, biallelic mutation of CEBPA status, and mutation status of BCOR, DNMT3A, FLT3-TKD, GATA2, RUNX1, SMC1A, and WT1. For OS those variables were: age, HG, white blood cell count, UPD of 11p, UPD of 13q, FLT3-ITD status, biallelic mutation of CEBPA status, and mutation status of DNMT3A, FLT3-TKD, GATA2, RUNX1, SMC1A, WT1 and ZRSR2.