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Table 4 Clinicopathological and molecular features of BRAF mutant colorectal cancers stratified according to methylator phenotype status.

From: BRAF mutations are associated with distinctive clinical, pathological and molecular features of colorectal cancer independently of microsatellite instability status

 

CIMP-

 

CIMP+

 

Feature

BRAF WT (n = 145) (%)

BRAF M (n = 5) (%)

P

BRAF WT (n = 31) (%)

BRAF M (n = 11) (%)

P

Age (years)

68.3 ± 13.5

71.0 ± 11.0

NS

71.7 ± 11.8

65.4 ± 26.3

NS

Females

37

60

NS

42

45

NS

TILS +

2

40

0.008

17

45

0.06

Node negative

63

60

NS

65

82

NS

Proximal site

35

60

NS

74

80

NS

Poor grade

13

66

0.05

20

40

NS

Mucinous

9

25

NS

25

45

NS

MSI+

6

20

NS

19

64

0.01

Dist. MLH1 methylated

3

0

NS

42

64

NS

Prox. MLH1 methylated

0

0

NS

23

55

0.05

KRAS mutant

43

0

0.06

55

0

0.001

TP53 mutant

26

0

NS

29

20

NS