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Table 1 Clinicopathologic and molecular characteristics of colorectal cancers according to the CIMP status

From: The CpG island methylator phenotype may confer a survival benefit in patients with stage II or III colorectal carcinomas receiving fluoropyrimidine-based adjuvant chemotherapy

 

CIMP-low/negative

(n = 211)

CIMP-high

(n = 34)

Pvalue

Age (yrs)

  

0.388

   Mean ± SD

59.7 ± 11.9

61.6 ± 11.9

 

   Median (range)

62.0 (29 - 83)

63.5 (33 - 82)

 

Gender (%)

  

0.752

   Male

118 (55.9)

20 (58.8)

 

   Female

93 (44.1)

14 (41.2)

 

Tumor site (%)

  

< 0.001

   Proximal

64 (30.3)

23 (67.6)

 

   Distal

147 (69.7)

11 (32.4)

 

Lymph node metastasis (%)

 

0.770

   Absent

106 (50.2)

18 (52.9)

 

   Present

105 (49.8)

16 (47.1)

 

AJCC stage (%)

  

0.548

   I/II

100 (47.4)

18 (52.9)

 

   III/IV

111 (52.6)

16 (47.1)

 

Differentiation (%)

  

< 0.001

   Well/Moderate

191 (90.5)

21 (61.8)

 

   Poor/Mucinous

20 (9.5)

13 (38.2)

 

Mucinous histology (%)

  

0.045...

   Absent

202 (95.7)

28 (82.4)

 

   Present

9 (4.3)

6 (17.6)

 

BRAF (%)

  

< 0.001

   Wild type

209 (99.1)

25 (73.5)

 

   Mutation

2 (0.9)

9 (26.5)

 

KRAS (%)

  

0.894

   Wild type

139 (65.9)

22 (64.7)

 

   Mutation

72 (34.1)

12 (35.3)

 

MGMT methylation (%)

  

< 0.001

   Absent

153 (72.5)

12 (35.3)

 

   Present

58 (27.5)

22 (64.7)

 

MSI status (%)

  

< 0.001

   MSS/MSI-low

183 (86.7)

13 (38.2)

 

   MSI-high

28 (13.3)

21 (61.8)

 
  1. CIMP CpG island methylator phenotype, AJCC American Joint Committee on Cancer, MSI microsatellite instablity, MSS microsatellite stable.
  2. Bold numbers indicate features associated with CIMP-high colorectal cancers p values < 0.05 were adjusted with Bonferroni correction to correct for potential false positive results