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. 2015 Apr 1;125(25):3878–3885. doi: 10.1182/blood-2015-01-623447

Table 1.

Demographics

Characteristic DA60 (n = 602) DA90 (n = 604)
Age, y
 16-29 59 59
 30-39 65 66
 40-49 120 121
 50-59 199 199
 60+ 159 159
 Median 53 53
 Range 16-72 16-72
Sex
 Female 267 284
 Male 335 320
Diagnosis
 De novo 509 509
 Secondary 59 59
 MDS 34 36
World Health Organization PS
 0 401 403
 1 165 166
 2 20 21
 3 15 14
 4 1 0
White blood cell count
 0-9.9 320 312
 10-49.9 175 175
 50-99.9 65 65
 100+ 42 52
 Median 8.0 9.3
 Range 0.3-430.0 0.4-395.0
Cytogenetics
 Favorable 60 52
 Intermediate 410 417
 Adverse 96 109
 Unknown 36 26
FLT3 ITD
 WT 458 462
 Mutant 100 100
 Unknown 44 42
NPM1c
 WT 400 383
 Mutant 153 167
 Unknown 49 54
ITD/NPM1c
 ITD WT, NPM1c WT 356 349
 ITD WT, NPM1c mutant 97 102
 ITD mutant, NPM1c WT 44 34
 ITD mutant, NPM1c mutant 56 65
 Unknown 49 54
Post–course 1 risk score
 Good risk 80 63
 Standard risk 255 257
 Poor risk 219 214
 Not assessable* 48 70

WT, wild-type.

*

Post–course 1 validated risk score22 is not available for patients who had induction death, had missing cytogenetics, or in whom a response to course 1 was not available.