Table 1 Baseline characteristics.

From: Early replacement of re-induction therapy following failed intensive induction treatment enhances the therapeutic efficacy of newly diagnosed AML

 

Patients (n = 175)

Age, years

Median(IQR)

45 (34–54)

< 20

5 (2.9%)

20–29

23 (13.1%)

30–39

35 (20.0%)

40–49

44 (25.1%)

50–59

68 (28.9%)

Sex

Male

74 (42.3%)

Female

101 (57.7%)

Baseline bone marrrow blast cell proportion, %

Median (IQR)

56 (34.2–74.8%)

< 30%

34 (19.4%)

≥ 30% to < 50%

38 (21.7%)

≥ 50%

103 (58.8%)

Baseline peripheral white blood cell count, x 109/L

Median(IQR)

15.7 (5.9–48.5)

< 10

66 (37.7%)

≥ 10 to < 40

57 (32.6%)

≥ 40 to < 100

33 (18.9%)

≥ 100

19 (10.8%)

Selected molecular mutation

FLT3-ITD

40 (22.9%)

NPM1

31 (17.7%)

DNMT3A

24 (13.7%)

CEBPA

24 (13.7%)

TET2

14 (8%)

ASXL1

12 (6.9%)

IDH1

9 (5.1%)

IDH2

8 (4.6%)

TP53

3 (1.7%)

BCR-ABL

2 (1.1%)

ELN2017 risk category

Favourable

82 (46.9%)

Intermediate

65 (37.1%)

Adverse

28 (16.0%)

Cytogenetic risk category

Favourable

44 (25.2%)

Intermediate

102 (58.3%)

Adverse

16 (9.1%)

No mitosis

13 (7.4%)

ELN 2022 risk category

Favourable

79 (45.1%)

Intermediate

64 (36.6%)

Adverse

32 (18.3%)

Induction therapy regimen

DA

111 (63.4%)

IA

64 (36.6%)

Allo-HSCT, n

35 (20%)

Re-induction therapy regimen of NR patients

Venetoclax + azacitidine

9

Venetoclax + azacitidine + homoharringtonine

3

FLAG/CLAG

4

CAG

2

HA

2