Table 1

Comparisons of clinical characteristics, molecular features, and outcomes of older primary CN-AML patients with and without FLT3-ITD

CharacteristicFLT3-ITD (n = 72)FLT3-WT (n = 147)P
Age, y   .92 
    Median 68 69  
    Range 60-81 60-83  
Age group, n (%)   .67 
    60-69 y 41 (57) 78 (53)  
    ≥ 70 y 31 (43) 69 (47)  
Sex, no. of males (%) 36 (50) 75 (51) 1.00 
Race, n (%)   .81 
    White 66 (92) 129 (90)  
    Nonwhite 6 (8) 14 (10)  
Protocol,* n (%)    
    8525 11 (15) 10 (7)  
    8923 9 (13) 9 (6)  
    9420 3 (4) 3 (2)  
    9720 27 (38) 75 (51)  
    10201 22 (31) 50 (34)  
Hemoglobin, g/dL   .35 
    Median 9.7 9.4  
    Range 6.0-15.0 6.0-13.1  
Platelet count, ×109/L   .40 
    Median 60 72  
    Range 4-850 5-510  
WBC, ×109/L   < .001 
    Median 47.1 10.4  
    Range 0.9-450.0 0.9-198.0  
Blood blasts, %   < .001 
    Median 70 24  
    Range 0-99 0-96  
Bone marrow blasts, %   < .001 
    Median 82 57  
    Range 7-97 7-96  
Centrally reviewed FAB classification, n (%)    
    M0 0 (0) 4 (5)  
    M1 17 (35) 11 (13)  
    M2 9 (18) 31 (36)  
    M4 12 (24) 22 (26)  
    M5 11 (22) 12 (14)  
    M6 0 (0) 5 (6)  
Extramedullary involvement, n (%) 20 (29) 23 (16) .04 
NPM1, n (%)   < .001 
    Mutated 53 (74) 68 (46)  
    Wild-type 19 (26) 79 (54)  
WT1, n (%)   .001 
    Mutated 11 (15) 4 (3)  
    Wild-type 61 (85) 143 (97)  
CEBPA, n (%)   .53 
    Mutated 11 (15) 18 (12)  
    Wild-type 61 (85) 129 (88)  
MLL-PTD, n (%)   .50 
    Positive 2 (4) 8 (7)  
    Negative 53 (96) 104 (93)  
IDH1, n (%)   .25 
    Mutated 5 (9) 21 (17)  
    Wild-type 50 (91) 102 (83)  
IDH2, n (%)   .02 
    Mutated, R140 IDH2 8 (15) 29 (24) (IDH2-mutated vs IDH2-WT) 
    Mutated, R172 IDH2 0 (0) 10 (8)  
    Wild-type 47 (85) 84 (68)  
Outcome for all patients, no. 72 147  
    Complete remission rate, n (%) 48 (67) 103 (70) .64 
    Disease-free survival   .007 
        Median, y 0.5 1.0  
        Disease-free at 3 y, % (95% CI) 10 (4-21) 18 (12-26)  
    Overall survival   < .001 
        Median, y 0.8 1.4  
        Alive at 3 y, % (95% CI) 14 (7-23) 23 (16-30)  
Outcome for patients aged 60-69 y, no. 41 78  
    Complete remission rate, no. (%) 29 (71) 58 (75) .67 
    Disease-free survival   < .001 
        Median, y 0.4 1.0  
        Disease-free at 3 y, % (95% CI) 7 (1-20) 19 (10-30)  
    Overall survival   < .001 
        Median, y 0.6 1.4  
        Alive at 3 y, % (95% CI) 10 (3–21) 26 (16–36)  
Outcome for patients age ≥ 70 y, no. 31 69  
    Complete remission rate, no. (%) 19 (61) 45 (65) .82 
    Disease-free survival   .94 
        Median, y 0.9 1.0  
        Disease-free at 3 y, % (95% CI) 16 (4-35) 18 (8-30)  
    Overall survival   .71 
        Median, y 0.9 1.3  
        Alive at 3 y, % (95% CI) 19 (8-35) 20 (11-30)  
CharacteristicFLT3-ITD (n = 72)FLT3-WT (n = 147)P
Age, y   .92 
    Median 68 69  
    Range 60-81 60-83  
Age group, n (%)   .67 
    60-69 y 41 (57) 78 (53)  
    ≥ 70 y 31 (43) 69 (47)  
Sex, no. of males (%) 36 (50) 75 (51) 1.00 
Race, n (%)   .81 
    White 66 (92) 129 (90)  
    Nonwhite 6 (8) 14 (10)  
Protocol,* n (%)    
    8525 11 (15) 10 (7)  
    8923 9 (13) 9 (6)  
    9420 3 (4) 3 (2)  
    9720 27 (38) 75 (51)  
    10201 22 (31) 50 (34)  
Hemoglobin, g/dL   .35 
    Median 9.7 9.4  
    Range 6.0-15.0 6.0-13.1  
Platelet count, ×109/L   .40 
    Median 60 72  
    Range 4-850 5-510  
WBC, ×109/L   < .001 
    Median 47.1 10.4  
    Range 0.9-450.0 0.9-198.0  
Blood blasts, %   < .001 
    Median 70 24  
    Range 0-99 0-96  
Bone marrow blasts, %   < .001 
    Median 82 57  
    Range 7-97 7-96  
Centrally reviewed FAB classification, n (%)    
    M0 0 (0) 4 (5)  
    M1 17 (35) 11 (13)  
    M2 9 (18) 31 (36)  
    M4 12 (24) 22 (26)  
    M5 11 (22) 12 (14)  
    M6 0 (0) 5 (6)  
Extramedullary involvement, n (%) 20 (29) 23 (16) .04 
NPM1, n (%)   < .001 
    Mutated 53 (74) 68 (46)  
    Wild-type 19 (26) 79 (54)  
WT1, n (%)   .001 
    Mutated 11 (15) 4 (3)  
    Wild-type 61 (85) 143 (97)  
CEBPA, n (%)   .53 
    Mutated 11 (15) 18 (12)  
    Wild-type 61 (85) 129 (88)  
MLL-PTD, n (%)   .50 
    Positive 2 (4) 8 (7)  
    Negative 53 (96) 104 (93)  
IDH1, n (%)   .25 
    Mutated 5 (9) 21 (17)  
    Wild-type 50 (91) 102 (83)  
IDH2, n (%)   .02 
    Mutated, R140 IDH2 8 (15) 29 (24) (IDH2-mutated vs IDH2-WT) 
    Mutated, R172 IDH2 0 (0) 10 (8)  
    Wild-type 47 (85) 84 (68)  
Outcome for all patients, no. 72 147  
    Complete remission rate, n (%) 48 (67) 103 (70) .64 
    Disease-free survival   .007 
        Median, y 0.5 1.0  
        Disease-free at 3 y, % (95% CI) 10 (4-21) 18 (12-26)  
    Overall survival   < .001 
        Median, y 0.8 1.4  
        Alive at 3 y, % (95% CI) 14 (7-23) 23 (16-30)  
Outcome for patients aged 60-69 y, no. 41 78  
    Complete remission rate, no. (%) 29 (71) 58 (75) .67 
    Disease-free survival   < .001 
        Median, y 0.4 1.0  
        Disease-free at 3 y, % (95% CI) 7 (1-20) 19 (10-30)  
    Overall survival   < .001 
        Median, y 0.6 1.4  
        Alive at 3 y, % (95% CI) 10 (3–21) 26 (16–36)  
Outcome for patients age ≥ 70 y, no. 31 69  
    Complete remission rate, no. (%) 19 (61) 45 (65) .82 
    Disease-free survival   .94 
        Median, y 0.9 1.0  
        Disease-free at 3 y, % (95% CI) 16 (4-35) 18 (8-30)  
    Overall survival   .71 
        Median, y 0.9 1.3  
        Alive at 3 y, % (95% CI) 19 (8-35) 20 (11-30)  

WBC indicates white blood count; FAB, French-American-British classification; FLT3-ITD, internal tandem duplication of the FLT3 gene; WT, wild-type; and MLL-PTD, partial tandem duplication of the MLL gene.

*

Cancer and Leukemia Group B frontline treatment protocol received. See supplemental material for details.

FLT3-ITD patients tended to have more extramedullary involvement, particularly in terms of gum hypertrophy and lymphadenopathy.

Median follow-up was 3.8 years (range, 2.3-11.6) for patients alive.

FLT3-ITD indicates internal tandem duplication of the FLT3 gene; WT, wild-type; and CI, confidence interval.

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