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. 2015 Mar 10;6(10):8144–8154. doi: 10.18632/oncotarget.3519

Table 1. Patients' characteristics in the CN-AML cohort according to the MAPKBP1 expression.

Variable MAPKBP1high, n=78 MAPKBP1low, n=79 P
Median age. y (range) 48.50 (18-77) 51 (16-73) 0.256
Female sex, no.(%) 37 (47.4) 36 (45.6) 0.87
FAB subtype, no.
M0 1 2 1
M1 28 17 0.05
M2 19 13 0.24
M3 1 0 0.50
M4 13 11 0.66
M5 14 25 0.06
M6 0 1 1
Other 2 10 0.03
FLT3-ITD, no. 50 16 <0.001
FLT3-TKD, no. 10 10 1
NPM1, no. 46 36 0.11
CEBPA, mutated, no.
Single 4 4 1
Double 5 11 0.18
N-RAS, mutated, no. 4 9 0.25
K-RAS, mutated, no. 0 1 1
IDH1, mutated, no. 10 9 0.81
IDH2, mutated, no. 5 8 0.81
ELN genetic group, no
Favorable 19 40 0.001
Intermediate-I 68 54 0.19
High ERG, no. 51 27 <0.001
High BAALC, no. 44 34 0.11
High LEF1, no. 33 45 0.35
High MN1, no. 42 36 0.34
High WT1, no. 54 24 <0.001
High DNMT3B, no. 55 23 <0.001
High TCF4, no. 54 24 <0.001

CN-AML indicates cytogenetically normal acute myeloid leukemia; FAB, French-American-British classification; ITD, internal tandem duplication; ELN, European Leukemia Net; and TKD, tyrosine kinase domain.

High ERG, BAALC, LEF1, MN1, WT1, DNMT3B and TCF4 expression were defined as an expression level above the median of all samples, respectively.