Table 2 Comparison of baseline characteristics among common U2AF1 mutations (N = 143).

From: U2AF1 pathogenic variants in myeloid neoplasms and precursor states: distribution of co-mutations and prognostic heterogeneity

Variables

S34F

(n = 97)

Q157P

(n = 46)

P value

Age

71 [25–92]

71 [53–92]

0.95

Age ≥70 years

56 (60)

26 (56.5)

0.85

High-risk myeloid neoplasm

26 (27)

13 (28)

>0.99

t-AML

17 (18)

7 (16)

0.81

CCUS

16 (16)

2 (4)

0.77

MDS

55 (57)

31 (67)

0.27

MDS/AML

10 (10)

4 (9)

0.77

AML

16 (17)

9 (20)

0.81

Hemoglobin (g/dl)

9.3 [6.4–13.3]

8.3 [5.8–13.1]

0.82

 ≤ 10.0

66 (69)

37 (80)

0.16

 ≤ 8.0

19 (20)

12 (26)

0.51

WBC (109/L)

2.4 [0.5–10.3]

2.9 [0.9–60]

0.23

Platelet (109/L)

93 [11–309]

83 [12–542]

0.72

 ≤ 100.0

51 (54)

24 (54.4)

>0.99

 ≤ 50.0

19 (20)

14 (32)

0.19

BM blast (%)

3 [0–83]

3.5 [0–90]

0.91

U2AF1 VAF (%)

33 [2–51]

38 [11–46]

0.37

CG abnormality

68 (70)

28 (62)

0.05

Co-mutation

71 (74)

42 (91)

0.01

 ASXL1

27 (28)

23 (50)

0.01

 BCOR

22 (23)

0

0.04

 RUNX1

11 (12)

9 (19)

0.46

 TET2

14 (15)

5 (11)

0.60

 DNMT3A

12 (12)

4 (9)

0.58

 RAS

8 (8)

2 (4)

0.50

 TP53

4 (4)

7 (15)

0.03

 JAK2

4 (4)

5 (11)

0.27

 SETBP1

5 (5)

4 (9)

0.47

 NPM1

1 (1)

0

>0.99

 FLT3 ITD

2 (2)

0

0.55

Two or more co-mutations

45 (47)

34 (73)

0.02

MDS patients progressing to AML

20/67 (30)

15/29 (52)

0.51

Treatment in high-risk myeloid neoplasm

 3 + 7

14 (20)

4 (13)

0.41

 HMA

41 (58)

15 (33)

0.09

 HMA plus venetoclax

4 (5.5)

5 (16)

0.72

Complete remission

19 (19.5)

7 (15)

>0.99

Allo-HCT

18 (19)

9 (21)

0.81

  1. t-AML therapy-related AML, CCUS clonal cytopenia of undetermined significance, CG cytogenetics, VAF variant allele frequency, HMA hypomethylating agent, CR complete remission, allo-HCT allogeneic hematopoietic stem cell transplantation.
  2. Bold values show statistically significant p values.