Skip to main content
. 2011 Oct 26;118(26):6920–6929. doi: 10.1182/blood-2011-08-368225

Table 1.

Comparison of clinical and molecular characteristics by ASXL1 mutation status in primary CN-AML patients 60 years of age or older

Variable ASXL1-mut (n = 38) ASXL1-wt (n = 182) P
Age, y .43
    Median 68 69
    Range 61-83 60-82
Male sex, no. (%) 24 (63) 85 (47) .08
Race, no. (%) .75
    White 34 (89) 164 (92)
    Nonwhite 4 (11) 15 (8)
WBC, × 109/L .02
    Median 10.6 28.1
    Range 0.9-173.1 0.9-450.0
Percent of blood blasts < .001
    Median 12 52
    Range 0-88 0-99
Percent of bone marrow blasts .04
    Median 52 67
    Range 8-93 4-97
Hemoglobin, g/dL .74
    Median 9.4 9.4
    Range 6.0-11.7 5.4-15.0
Platelet count, × 109/L .06
    Median 85 65
    Range 14-510 4-850
FAB category, no. (%)*
    M0 1 (4) 2 (2)
    M1 2 (8) 31 (25)
    M2 12 (50) 36 (29)
    M4 6 (25) 27 (22)
    M5 3 (13) 24 (20)
    M6 0 (0) 3 (2)
Extramedullary involvement, no. (%) 7 (18) 42 (23) .67
NPM1, no. (%) < .001
    Mutated 2 (5) 125 (69)
    Wild-type 36 (95) 57 (31)
FLT3-ITD, no. (%) .002
    Positive 4 (11) 66 (36)
    Negative 34 (89) 116 (64)
CEBPA, no. (%) .01
    Mutated 10 (26) 17 (9)
        Single mutated 5 11
        Double mutated 5 6
    Wild-type 28 (74) 165 (91)
ELN genetic category, no. (%) .08
    Favorable 12 (32) 87 (48)
    Intermediate-I 26 (68) 95 (52)
TET2, no. (%) 1.0
    Mutated 11 (29) 55 (30)
    Wild-type 27 (71) 126 (70)
IDH1, no. (%) 1.0
    Mutated 4 (11) 22 (12)
    Wild-type 34 (89) 159 (88)
IDH2, no. (%) .21
    IDH2 mutated 12 (32) 39 (22)
        Codon R140 mutation 10 31
        Codon R172 mutation 2 8
    Wild-type 26 (68) 142 (78)
FLT3-TKD, no. (%) .54
    Present 2 (5) 18 (10)
    Absent 36 (95) 164 (90)
WT1, no. (%) .48
    Mutated 1 (3) 14 (8)
    Wild-type 37 (97) 168 (92)
MLL-PTD, no. (%) .28
    Present 4 (11) 9 (6)
    Absent 31 (89) 139 (94)

FAB indicates French-American-British classification; and —, not applicable.

*

FAB categories are centrally reviewed

Within CN-AML patients, the ELN Favorable group is defined as patients with mutated CEBPA and/or mutated NPM1 without FLT3-ITD. All remaining CN-AML patients (ie, those with wild-type CEBPA, and FLT3-ITD and/or wild-type NPM1) belong to the ELN Intermediate-I category.27