Table 2.

Baseline characteristics of the AML cohort

VariableNumber
Patients included 88 
Age, mean (range), y 43.6 (18-74) 
Sex (%)  
Male 50 
Female 50 
AML type (%)  
Acute promyelocytic leukemia 27 
AML with mutated NPM1 15 
AML with RUNX1-RUNXT1 
AML with CBFB-MYH11 
AML with biallelic mutation of CEBPA 
Other AML with recurrent genetic abnormalities 
AML not otherwise specified 40 
Non-APL AML risk stratification (ELN 2017, %)  
Favorable 34 
Intermediate 36 
Adverse 30 
APL risk stratification (GIMEMA/PETHEMA 2000, %)  
Favorable 
Intermediate 15 
Adverse 81 
VariableNumber
Patients included 88 
Age, mean (range), y 43.6 (18-74) 
Sex (%)  
Male 50 
Female 50 
AML type (%)  
Acute promyelocytic leukemia 27 
AML with mutated NPM1 15 
AML with RUNX1-RUNXT1 
AML with CBFB-MYH11 
AML with biallelic mutation of CEBPA 
Other AML with recurrent genetic abnormalities 
AML not otherwise specified 40 
Non-APL AML risk stratification (ELN 2017, %)  
Favorable 34 
Intermediate 36 
Adverse 30 
APL risk stratification (GIMEMA/PETHEMA 2000, %)  
Favorable 
Intermediate 15 
Adverse 81 

ELN, European LeukemiaNet; GIMEMA, Gruppo Italiano Malattie EMatologiche dell’Adulto; PETHEMA, Programa de Estudio y Tratamiento de las Hemopatías Malignas.

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