Table 2.
Clinical characteristics of primary AML samples.
| AML Sample | Clinical Characteristics | NKG2D-L SFI |
|---|---|---|
| 1 | 29yo M; 73% BM blasts; FAB M4-Eo; Complex karyotype with inversion 16. CBFB rearrangement by FISH |
1.04 |
| 2 | 49yo F; 21% BM blasts; relapsed FLT-3 mutated AML Normal karyotype and cytogenetics |
1.02 |
| 3 | 31yo M; 30% BM blasts; acute erythroid/myeloid leukemia 3q inversion and monosomy 7 |
0.97 |
| 4 | 45yo F, BM 76% blasts; relapsed AML s/p NMA allo-SCT; 5q deletion |
1.08 |
| 5 | 47yo F, 91% BM blasts; secondary t-AML; FAB M1 Near tetraploidy |
1.07 |
| 6 | 65yo M; 39% BM blasts, FAB M4 Normal cytogenetics |
0.97 |
| 7 | 68yo F; 70% BM blasts, FAB M1 Normal cytogenetics |
1.12 |
| 8 | 54yo F; 64% BM blasts; secondary AML arising from MDS | 1.05 |
| 9 | 39yo F, 16% BM blasts, FAB M6 (6;9) translocation |
1.02 |
| 10 | 55yo M, 22% BM blasts, secondary AML arising from MDS Normal cytogenetics |
1.02 |
| 11 | 49yo F; 40% BM blasts; FAB M4 MLL rearranged, FLT-3 WT (negative) |
0.88 |
| 12 | 60yo M, 20% BM blasts, relapsed AML, FAB M2 Normal cytogenetics |
1.04 |
| 13 | 30yo M, 26% blasts, relapsed AML, FAB M2, FLT-3 ITD+ 13q deletion, |
0.93 |
| 14 | 52yo M; BM 43% BM blasts, FAB M2 | 1.42 |
| 15 | 21yo M; BM 86% blasts, FAB M4 Clonal rearrangement of 7p; 9q deletion. |
1.19 |
| 16 | 53yo M, 40% BM blasts; relapsed AML, FAB M4, FLT-3 mutated Normal cytogenetics |
1.08 |
| 17 | 53yo M; 42% BM blasts, FAB M2 Normal cytogenetics |
1.62 |
| 18 | 23yo F; BM blasts 70% Inversion 16 |
1.13 |
| 19 | 23yo F; BM blasts 70%; Molecular: FLT-3 ITD+, RUNX1, DNMT3 and ASXL1 mutations Normal cytogenetics |
1.06 |
| 20 | 72yo M; 67% BM blasts Normal cytogenetics |
1.38 |
| 21 | 67yo M; 50% BM Blasts; FAB M4; Molecular: NMP1 mutated Normal cytogenetics |
1.21 |
| 22 | 27yo F; 82% BM blasts; molecular: CEBPA mutation Cytogenetics: trisomy 21 |
1.04 |
| 23 | 45yo M; 69% BM Blasts, FAB M4-Eo; FLT3 D835 mutation (negative for FLT3-ITD and NPM1) Inversion 16 |
2.01 |
| 24 | 64yo F; 60% BM blasts; FAB M4 Molecular: DNMT3A, WT1 mutations Cytogenetics: +8 |
1.18 |