Skip to main content
. 2020 Aug 20;36(2):401–412. doi: 10.3904/kjim.2020.014

Table 1.

Baseline characteristics

Characteristic Total De novo AML Secondary AML p value
Number of patients 52 40 12 NA
Age, yr 62 (23–88) 63 (23–88) 60 (40–81) 0.656
 ≤ 65 33 (63.5) 26 (65.0) 7 (58.3)
 > 65 19 (36.5) 14 (35.0) 5 (41.7)
Sex, male 33 (63.5) 26 (65.0) 7 (58.3) 0.674
Cytogenetic risk
Low 6 (11.5) 6 (15.0) 0 (0.0) 0.001
 Intermediate 38 (73.1) 32 (80.0) 6 (50.0)
 High 8 (15.4) 2 (5.0) 6 (50.0)
Combined riska
 Low 7 (13.5) 7 (17.5) 0 0.037
 Intermediate 19 (36.5) 15 (37.5) 4 (33.3)
 High 12 (23.1) 6 (15.0) 6 (50.0)
 Unknown 14 (26.9) 12 (30.0) 2 (16.7)
Extramedullary involve 0 0 0 NA
Laboratory findings
 Bone marrow blast, % 63.7 ± 22.4 66.5 ± 20.2 54.5 ± 27.6 0.281
 WBC count, /L 29,169 ± 54,648 31,740 ± 61,259 20,599 ± 20,903 0.334
 Platelet count, × 109/L 86.1 ± 72.0 81.3 ± 52.5 102.1 ± 117.9 0.564
 Hemoglobin, g/dL 9.2 ± 2.0 9.0 ± 2.0 9.8 ± 2.2 0.292

Values are presented as median (range), number (%), or mean ± standard deviation.

AML, acute myeloid leukemia; NA, not applicable; WBC, white blood cell.

a

Combined risk refers to risk stratification based on available next generation sequencing data including TP53, ASXL1, RUNX1 mutation status.