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Table 1 Patients’ characteristics and TP53 mutation in 132 patients with AML/ MDS

From: TP53 mutation in newly diagnosed acute myeloid leukemia and myelodysplastic syndrome

Factors

Number of AML/ MDS patients

N (%)

TP53 mutated patients

N (%)

P

Age, range 16–93 years (N = 132)

  

0.575

 < 60 years

69 (52.3)

6/69 (8.7)

 

> 60 years

63 (47.7)

8//63 (12.7)

 

Disease (N = 132)

  

0.003

 De novo AML

87 (65.9)

8/87 (9.2)

 

 Secondary AML

17 (12.9)

3/17 (17.6)

 

 MDS (excess blast)

24 (18.2)

1/24 (4.2)

 

 T-AML/MDS

4 (3.0)

2/4 (50)

 

White blood cell count in AML patients (N = 107)

  

0.563

 < 100,000/μL

88 (82.2)

12/88 (13.6)

 

> 100,000/μL

19 (17.8)

0/19 (0)

 

Chromosome analysis (N = 132)

  

0.016

 Abnormal

67 (50.8)

12//67 (17.9)

 

 Normal

65 (49.2)

2/65 (3.1)

 

Cytogenetic risk (N = 132)

  

0.01

 Favorable

6 (4.5)

0/6 (0)

 

 Intermediate

89 (67.4)

5/89 (5.6)

 

 Unfavorable

37 (28)

9/37 (24.3)

 

Complex chromosome (N = 132)

  

0.004

 Yes

24 (18.2)

7/24 (29.2)

 

 No

108 (81.8)

7/108 (6.5)

 

Complex with monosomy karyotype (N = 132)

  

0.008

 Yes

14 (10.6)

5/14 (35.7)

 

 No

118 (89.4)

9/118 (7.6)

 

Complex with del5/−5 or del7/−7 (N = 132)

  

0.026

 Yes

12 (9.0)

4/12 (33.3)

 

 No

120 (91.0)

10/120 (8.3)

 

Monosomy (N = 132)

  

0.002

 Yes

21 (15.9)

7/21 (33.3)

 

 No

111 (84.1)

7/111 (6.3)

 

Gene mutation (N = 107 AML patients)

  

0.893

 FLT3-ITD

13 (12.1)

3/13 (23)

 

 NPM1

26 (24.3)

3/26 (11.5)

 

 CEBPA

9 (8.4)

0/9 (0)

 

 No mutation

80 (74.8)

10/80 (12.5)