Clinical and molecular features of younger adult patients with cytogenetically normal AML (N = 365)
Characteristic . | Summary statistics . |
---|---|
Age, y | |
Median | 46 |
Range | 17-59 |
Sex, n (%) | |
Male | 188 (52) |
Female | 177 (48) |
Race, n (%) | |
White | 324 (91) |
Nonwhite | 34 (9) |
Hemoglobin, g/dL | |
Median | 9.2 |
Range | 4.2-25.1 |
Platelet count, ×109/L | |
Median | 56 |
Range | 8-445 |
WBC count, ×109/L | |
Median | 28.8 |
Range | 0.6-475.0 |
Blood blasts, % | |
Median | 60 |
Range | 0-97 |
BM blasts, % | |
Median | 68 |
Range | 18-96 |
Extramedullary involvement, n (%) | |
Present | 106 (30) |
Absent | 250 (70) |
ASXL1, n (%) | |
Mutated | 12 (3) |
Wild type | 334 (97) |
CEBPA, n (%) | |
Double mutated | 54 (16) |
Wild type | 294 (84) |
DNMT3A, n (%) | |
Mutated | 139 (39) |
R882 | 105 |
Non-R882 | 34 |
Wild type | 213 (61) |
FLT3-ITD, n (%) | |
Present | 137 (38) |
Absent | 221 (62) |
FLT3-TKD, n (%) | |
Present | 36 (10) |
Absent | 314 (90) |
IDH1, n (%) | |
Mutated | 27 (8) |
Wild type | 325 (92) |
IDH2, n (%) | |
Mutated | 34 (10) |
Wild type | 318 (90) |
NPM1, n (%) | |
Mutated | 201 (58) |
Wild type | 143 (42) |
RUNX1, n (%) | |
Mutated | 19 (5) |
Wild type | 333 (95) |
SF1, n (%) | |
Mutated | 2 (1) |
Wild type | 350 (99) |
SF3A1, n (%) | |
Mutated | 1 (0) |
Wild type | 351 (100) |
SF3B1, n (%) | |
Mutated | 10 (3) |
Wild type | 342 (97) |
SRSF2, n (%) | |
Mutated | 11 (3) |
Wild type | 339 (97) |
TET2, n (%) | |
Mutated | 40 (11) |
Wild type | 312 (89) |
U2AF1, n (%) | |
Mutated | 4 (1) |
Wild type | 348 (99) |
U2AF2, n (%) | |
Mutated | 0 (0) |
Wild type | 352 (100) |
WT1, n (%) | |
Mutated | 39 (11) |
Wild type | 313 (89) |
ZRSR2, n (%) | |
Mutated | 15 (4) |
Wild type | 337 (96) |
ELN genetic group*, n (%) | |
Favorable | 199 (59) |
Intermediate | 88 (26) |
Adverse | 52 (15) |
NPM1 and DNMT3A, n (%) | |
Either or neither mutated | 239 (69) |
Both mutated | 105 (31) |
NPM1 and FLT3-ITD, n (%) | |
Either or neither mutated | 252 (74) |
Both mutated | 89 (26) |
ERG expression group†, n (%) | |
High | 184 (51) |
Low | 178 (49) |
BAALC expression group†, n (%) | |
High | 168 (50) |
Low | 166 (50) |
MN1 expression group†, n (%) | |
High | 176 (50) |
Low | 173 (50) |
miR-181a expression group†, n (%) | |
High | 148 (50) |
Low | 147 (50) |
miR-3151, n (%) | |
Expressed | 51 (17) |
Not expressed | 244 (83) |
miR-155 expression group†, n (%) | |
High | 147 (50) |
Low | 148 (50) |
Characteristic . | Summary statistics . |
---|---|
Age, y | |
Median | 46 |
Range | 17-59 |
Sex, n (%) | |
Male | 188 (52) |
Female | 177 (48) |
Race, n (%) | |
White | 324 (91) |
Nonwhite | 34 (9) |
Hemoglobin, g/dL | |
Median | 9.2 |
Range | 4.2-25.1 |
Platelet count, ×109/L | |
Median | 56 |
Range | 8-445 |
WBC count, ×109/L | |
Median | 28.8 |
Range | 0.6-475.0 |
Blood blasts, % | |
Median | 60 |
Range | 0-97 |
BM blasts, % | |
Median | 68 |
Range | 18-96 |
Extramedullary involvement, n (%) | |
Present | 106 (30) |
Absent | 250 (70) |
ASXL1, n (%) | |
Mutated | 12 (3) |
Wild type | 334 (97) |
CEBPA, n (%) | |
Double mutated | 54 (16) |
Wild type | 294 (84) |
DNMT3A, n (%) | |
Mutated | 139 (39) |
R882 | 105 |
Non-R882 | 34 |
Wild type | 213 (61) |
FLT3-ITD, n (%) | |
Present | 137 (38) |
Absent | 221 (62) |
FLT3-TKD, n (%) | |
Present | 36 (10) |
Absent | 314 (90) |
IDH1, n (%) | |
Mutated | 27 (8) |
Wild type | 325 (92) |
IDH2, n (%) | |
Mutated | 34 (10) |
Wild type | 318 (90) |
NPM1, n (%) | |
Mutated | 201 (58) |
Wild type | 143 (42) |
RUNX1, n (%) | |
Mutated | 19 (5) |
Wild type | 333 (95) |
SF1, n (%) | |
Mutated | 2 (1) |
Wild type | 350 (99) |
SF3A1, n (%) | |
Mutated | 1 (0) |
Wild type | 351 (100) |
SF3B1, n (%) | |
Mutated | 10 (3) |
Wild type | 342 (97) |
SRSF2, n (%) | |
Mutated | 11 (3) |
Wild type | 339 (97) |
TET2, n (%) | |
Mutated | 40 (11) |
Wild type | 312 (89) |
U2AF1, n (%) | |
Mutated | 4 (1) |
Wild type | 348 (99) |
U2AF2, n (%) | |
Mutated | 0 (0) |
Wild type | 352 (100) |
WT1, n (%) | |
Mutated | 39 (11) |
Wild type | 313 (89) |
ZRSR2, n (%) | |
Mutated | 15 (4) |
Wild type | 337 (96) |
ELN genetic group*, n (%) | |
Favorable | 199 (59) |
Intermediate | 88 (26) |
Adverse | 52 (15) |
NPM1 and DNMT3A, n (%) | |
Either or neither mutated | 239 (69) |
Both mutated | 105 (31) |
NPM1 and FLT3-ITD, n (%) | |
Either or neither mutated | 252 (74) |
Both mutated | 89 (26) |
ERG expression group†, n (%) | |
High | 184 (51) |
Low | 178 (49) |
BAALC expression group†, n (%) | |
High | 168 (50) |
Low | 166 (50) |
MN1 expression group†, n (%) | |
High | 176 (50) |
Low | 173 (50) |
miR-181a expression group†, n (%) | |
High | 148 (50) |
Low | 147 (50) |
miR-3151, n (%) | |
Expressed | 51 (17) |
Not expressed | 244 (83) |
miR-155 expression group†, n (%) | |
High | 147 (50) |
Low | 148 (50) |
ELN, European LeukemiaNet; WBC, white blood cell count.
Among patients with CN-AML, the ELN favorable-risk category comprises patients with double-mutated CEBPA and patients with mutated NPM1 without FLT3-ITD or with FLT3-ITDlow. The ELN intermediate-risk category includes patients with wild-type or single-mutated CEBPA, patients with wild-type NPM1 without FLT3-ITD or with FLT3-ITDlow, and/or patients with mutated NPM1 and FLT3-ITDhigh. The ELN adverse-risk category comprises patients with wild-type or single-mutated CEBPA and wild-type NPM1 with FLT3-ITDhigh, patients with mutated RUNX1 and/or ASXL1 (if these mutations do not co-occur with favorable-risk subtypes), and/or patients with mutated TP53. FLT3-ITDlow is defined by an FLT3-ITD/FLT3 wild-type allelic ratio of <0.5, and FLT3-ITDhigh is defined by an FLT3-ITD/FLT3 wild-type allelic ratio of ≥0.5.
The median expression value was used as a cut point.