From: FLT3mutation incidence and timing of origin in a population case series of pediatric leukemia
Patient ID | ITD or MUT* | MUT | Age | Cytogenetics | FAB (lineage) | Backtrack result†|
---|---|---|---|---|---|---|
0004 | ITD | Â | 6.1 | 46, XY [10/20]; 46, XY, del(9)(p13) [9/20]; 47, XY, +?22 [1/20] | ALL | neg |
0087 | ITD | Â | 10.5 | 46, XY [21/24] | AML-M1 | neg |
0104 | ITD | Â | 9.1 | 46, XY [19/20]; 44, XY, -14, -22 [1/20] | ALL-L1 (T-cell) | neg |
0126 | ITD | Â | 14.9 | 46, XX [20/20] | AML-M2 | Â |
0201 | MUT | GAT→GAA D835E | 13.2 | 46, XY [20/20] | AML-M2 |  |
0261 | ITD | Â | 13.7 | 46, XX, t(6;9)(p23;q34) [23/24] | AML-M2 | neg |
0544 ‡ | MUT | GAT→GTT D835V | 5.3 | 46, XX [20/20]; nuc ish 12p13(TEL×2), 21q22(AML1×4) [149/207]/12p13(TEL×2), 21q22(AML×2) [31/207]/12p13(TEL×2), 21q22(AML1×3) [25/207] | ALL | neg |
0678 | ITD | Â | 14.5 | 46, XX [20] | AML-M2 | Â |
0738 | MUT | TAT→TGT Y842C | 5.0 | 45, XY, -7, del(13)(q13q21) [12/20]; 46, XY [8/20] | ALL-L1 |  |
0745 | MUT | GAT→TAT D835Y | 12.7 | 46, XY [21/21]; nuc ish 4cen(CEP4×2), 10cen(CEP10×2), 12p13(TEL×2), 21q22(AML1×2) | ALL-L1/L2 |  |
0796 ‡ | MUT | GAT→TAT D835Y | 1.8 | 46, XY [3/3]; nuc ish 12p13 (TEL×3), 21q22(AML1×4) [90/100], 12p13(TEL×2), 21q22(AML1×2) [10/100] FISH: +12++21/++X (presumed cryptic high hyperdiploidy) | ALL-L1 | neg |
0803 | MUT | GAT→TAT D835Y and GAT→CAT D835H | 0.3 | 46, XY [20/20]; nuc ish 11q23 (MLL5'x2, MLL3'x2) [200/200] | AML-M5 |  |
0945 ‡ | MUT | GAT→TAT D835Y | 7.9 | 46, XY [21/21] | ALL | neg |
0999 | ITD | Â | 8.3 | 46, XX [20] | AML | Â |
1043 | MUT | GAT→CAT D835H | 14.0 | 46, XY, inv(16)(p12q22) [12/12] | AML |  |
1073 ‡ | DEL |  | 5.9 | 46, XY [30]; nuc ish 9q34(ABL×2), 22q11.2(BCR×2) | ALL | neg |
1107 ‡§ | MUT | GAT→GCT D835A | 3.5 | 56~58, XY, dup(1)(q21q32),+4,+5,+6,+10,+14,+18,+18,+19,+21, +22,+2mar [5/23]; 46, XY [18/23] | ALL-L1 |  |
1148 | ITD | Â | 14.5 | 47, XX, +14 [16] | AML | neg |