Table 2.

Cox proportional hazard model univariable analysis for OS and EFS in all patients

OS, HR (95% CI)EFS, HR (95% CI)
Age 0.99 (0.96-1.02) 0.98 (0.96-1.00) 
AML (other vs de novo) 3.58 (1.20-10.7) 1.87 (0.8-4.39) 
DNMT3A mutated vs wild type 0.79 (0.45-1.37) 0.95 (0.7-1.29) 
FLT3-ITD mutated vs wild type 2.50 (1.06-5.86) 1.87 (1.06-3.28) 
N/KRAS mutations vs wild type 1.23 (0.28-5.38) 0.59 (0.18-1.90) 
IDH1/2 mutations vs wild type 1 (0.41-2.42) 1.33 (0.76-2.33) 
Molecular progression vs molecular persistence 1.54 (0.38-1.75) 0.71 (0.27-1.89) 
Molecular relapse vs molecular persistence 2.09 (0.79-5.58) 1.13 (0.63-2.01) 
More than 365 NPM1 copies /105 ABL at relapse (vs ≤365 copies) 1.51 (0.64-3.53) 1.01 (0.59-1.72) 
Venetoclax combination (LDAC vs AZA) 0.87 (0.38-6.16) 0.86 (0.50-1.49) 
Allogeneic HSCT after treatment vs no HSCT 1.28 (0.52-3.16) 0.81 (0.43-1.56) 
OS, HR (95% CI)EFS, HR (95% CI)
Age 0.99 (0.96-1.02) 0.98 (0.96-1.00) 
AML (other vs de novo) 3.58 (1.20-10.7) 1.87 (0.8-4.39) 
DNMT3A mutated vs wild type 0.79 (0.45-1.37) 0.95 (0.7-1.29) 
FLT3-ITD mutated vs wild type 2.50 (1.06-5.86) 1.87 (1.06-3.28) 
N/KRAS mutations vs wild type 1.23 (0.28-5.38) 0.59 (0.18-1.90) 
IDH1/2 mutations vs wild type 1 (0.41-2.42) 1.33 (0.76-2.33) 
Molecular progression vs molecular persistence 1.54 (0.38-1.75) 0.71 (0.27-1.89) 
Molecular relapse vs molecular persistence 2.09 (0.79-5.58) 1.13 (0.63-2.01) 
More than 365 NPM1 copies /105 ABL at relapse (vs ≤365 copies) 1.51 (0.64-3.53) 1.01 (0.59-1.72) 
Venetoclax combination (LDAC vs AZA) 0.87 (0.38-6.16) 0.86 (0.50-1.49) 
Allogeneic HSCT after treatment vs no HSCT 1.28 (0.52-3.16) 0.81 (0.43-1.56) 

AZA, azacitidine.

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