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. 2010 Jan 7;115(12):2372–2379. doi: 10.1182/blood-2009-09-241075

Table 2.

Clinical characteristics and CR rates for patients with CBF AML with and without KIT mutations

KIT mutation+ WT KIT P
Total, n 38 165
Sex
    Male, n (%) 22 (58) 84 (51) .437
    Female, n (%) 16 (42) 81 (49)
Age, y
    Median (range) 10.5 (1.1-16.6) 12.0 (0.6-19.6) .127
    0 to younger than 2 y, n (%) 4 (11) 6 (4) .077
    2 to younger than 10 y, n (%) 14 (37) 55 (33) .681
    10-21 y, n (%) 20 (53) 104 (63) .236
Race
    White, n (%) 23 (61) 108 (66) .504
    Nonwhite, n (%) 15 (39) 55 (34)
    Unknown, n 0 2
WBC count, median (range) 33.5 (3.9-379) 27.1 (1.6-373) .477
BM blasts, %, median (range) 56 (0-92) 52 (0-99) .915
Additional mutations
    FLT3/ITD
        Negative, n (%) 31 (100) 139 (96) .592
        Positive, n (%) 0 (0) 6 (4)
    NPM1
        Negative, n (%) 17 (100) 110 (100) > .999
        Positive, n (%) 0 (0) 0 (0)
    CEBPA
        Negative, n (%) 21 (100) 103 (100) > .999
        Positive, n (%) 0 (0) 0 (0%)
    WT-1
        Negative, n (%) 22 (100) 96 (88) .124
        Positive, n (%) 0 (0) 13 (12)
        BM blasts, %, median (range) 56 (0-92) 52 (0-99) .195
Induction response
    CR, n (%) 36 (97) 144 (94) .690
    Not in CR, n (%) 1 (3) 9 (6)
    Unevaluable or withdrew, n 1 12

CBF AML indicates core binding factor acute myeloid leukemia; WT, wild-type; WBC, white blood cell; BM, bone marrow; FLT3/ITD, FLT3 internal tandem duplication; NPM1, nucleophosmin; CEBPA, CCAAT/enhancer binding protein-α; WT-1, Wilms tumor gene 1; and CR, complete remission.