Summary of the AML patients screened for PU.1 mutations
AML phenotype . | FAB . | n2-155 . | Mutations . |
---|---|---|---|
Undifferentiated | M0 | 13 | 3 |
Myeloblastic | M1 | 8 | 12-153 |
M2 | 23* | 0 | |
Promyelocytic | M3 | 11‡ | 0 |
Myelomonocytic | M4 | 49† | 3 |
Monoblastic | M5 | 14 | 1 |
Erythroleukemia | M6 | 6 | 1 |
AUL | 2 | 0 | |
Total | 126 |
AML phenotype . | FAB . | n2-155 . | Mutations . |
---|---|---|---|
Undifferentiated | M0 | 13 | 3 |
Myeloblastic | M1 | 8 | 12-153 |
M2 | 23* | 0 | |
Promyelocytic | M3 | 11‡ | 0 |
Myelomonocytic | M4 | 49† | 3 |
Monoblastic | M5 | 14 | 1 |
Erythroleukemia | M6 | 6 | 1 |
AUL | 2 | 0 | |
Total | 126 |
Subtypes according to the French-American-British (FAB) classification.
Of the 23 M2 patients, 3 were positive for the AML1-ETO translocation.
Of the 49 M4 patients, 10 carried the inv(16).
All 11 M3 patients had the PML-RARA translocation.
This patient was originally classified as M4.
n indicates the number of patients with this subtype.