Table 1.
Patient # | Age | Sex | AML subtype | Recurrent Genetic Abnormalities | Cell Source |
---|---|---|---|---|---|
1 | 41 | F | M4 | FLT3-ITD, NPM1c, c-Kit | BM |
2 | 61 | M | M4 | FLT3-ITD, NPM1c | BM |
3 | 33 | M | M3 | PML/RARA | BM |
4 | 55 | M | AML-MRC | NPM1c, CEBPA | BM |
5 | 70 | M | AML-MRC | NRAS, SF3B1, ETV6 | BM |
6 | 65 | M | M2 | None were identified | BM |
7 | 73 | M | M2 | Tet2 | BM |
8 | 42 | M | M2 | FLT3-ITD, c-Kit | BM |
9 | 33 | F | M5 | None were identified | BM |
10 | 84 | F | M1 | IDH1 | BM |
11 | 51 | M | M0 | None were identified | BM |
12 | 49 | M | M2 | FLT3-ITD, c-Kit | PB |
13 | 71 | M | M4 | None were identified | BM |
14 | 76 | M | AML-MRC | None were identified | BM |
15 | 74 | M | M4 | NPM1c | PB |
16 | 14 | M | M4 | None were identified | BM |
17 | NA | NA | NA | NA | BM |
AML-MRC, AML with myelodysplasia related changes; BM, Bone marrow; PB, Peripheral Blood; NA, Data not available.