Table 3 Univariate and multivariate analysis for overall survival in patient with high-risk myeloid neoplasm with S34F and Q157P mutations (n = 39).

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

Variables

Univariate analysis

Multivariate analysis

Hazard ratio

95% CI

P value

Hazard ratio

95% CI

P value

Age ≥70 years

1.82

0.82–4.0

0.11

BM blast ≥ 20% vs 10–19%

2.31

1.04–5.11

0.03

1.39

0.58–3.35

0.45

t-AML

0.75

0.30–1.81

0.37

   

U2AF1 mutations: Q157P vs S34F

2.64

1.08–6.47

0.008

4.37

1.31–14.11

0.01

CG abnormality

1.37

0.59–3.15

0.46

-

-

 ASXL1

2.69

1.05–6.86

0.008

0.49

0.15–1.56

0.23

 BCOR

0.48

0.19–1.20

0.12

 RUNX1

1.24

0.47–3.29

0.65

 TET2

0.83

0.30–2.29

0.72

 DNMT3A

0.49

0.30–1.69

0.72

 RAS

0.88

0.35–2.20

0.80

 TP53

1.06

0.31–3.65

0.91

 JAK2

4.90

0.24–98.1

0.01

8.12

1.39–47.31

0.02

 SETBP1

0.38

0.10–1.40

0.32

 FLT3 ITD

2.47

0.42–14.46

0.11

Two or more co-mutations

0.97

0.48–1.97

0.94

Treatment in high-risk MDS/AML

 3 + 7

0.66

0.35–1.26

0.71

 HMA

0.33

0.70–2.02

0.33

 HMA plus venetoclax

1.31

0.56–3.07

0.82

Complete remission (CR/CRi)

0.77

0.38–1.55

0.47

Allo-HCT

0.41

0.19–0.92

0.05

0.71

0.09–0.57

0.01

  1. VAF variant allele frequency, HMA hypomethylating agent, CR complete remission, PR partial remission, HI hematological improvement.
  2. Bold values show statistically significant p values.