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Table 1 Demographic, anatomopathological and biological data of the cohort. Twenty-three colorectal cancer tumor tissues were included and 22 circulating tumor DNA. For 11 of the tumor tissues, non-tumor tissues close to the tumor were analyzed. The anatomopathological and biological results come from analyses carried out as part of patient management

From: The detection of specific hypermethylated WIF1 and NPY genes in circulating DNA by crystal digital PCR™ is a powerful new tool for colorectal cancer diagnosis and screening

 

Tumor/non-tumor tissues pairs (n = 11)

Tumor tissues (n = 12)

ctDNA (n = 22)

Sex, n (%)

 Men

5 (45%)

6 (50%)

16 (73%)

 Women

6 (55%)

6 (50%)

6 (27%)

Age in years, mean (min-max)

 

60 (44–79)

75 (55–84)

63 (36–82)

Location of the tumor, n (%)

 Duodenum

/

1 (8%)

/

 Cecum

2 (18%)

2 (17%)

2 (9%)

 Right colon

2 (18%)

6 (50%)

3 (13%)

 Transverse colon

/

2 (17%)

1 (5%)

 Left colon

5 (46%)

/

11 (50%)

 Rectosigmoid junction

1 (9%)

1 (8%)

1 (5%)

 Rectum

1 (9%)

/

4 (18%)

Conservation, n (%)

 FFPE

8 (72%)

12 (100%)

/

 Freezing

3 (28%)

/

/

Histology, n (%)

 ADC

11 (100%)

12 (100%)

19 (86%)

 Tubular adenoma

/

/

1 (5%)

 NA

/

/

2 (9%)

Stage, n (%)

 I

1 (9%)

2 (17%)

2 (9%)

 II

4 (37%)

5 (42%)

/

 III

3 (27%)

2 (17%)

/

 IV

3 (27%)

2 (17%)

20 (91%)

 ND

/

1 (8%)

/

Microsatellite stability, n (%)

 MSS

7 (64%)

2 (17%)

16 (72%)

 MSI

3 (27%)

10 (83%)

1 (5%)

 NA

1 (9%)

/

5 (23%)

Mutational status, n (%)

KRAS mutation

3 (27%)

3 (25%)

7 (32%)

NRAS mutation

/

/

2 (9%)

BRAF mutation

3 (27%)

4 (33%)

1 (5%)

 Other mutations

/

/

1 (5%)

 No mutation

1 (9%)

5 (42%)

11 (50%)

 NA

4 (36%)

/

/

MLH1 methylation, n (%)

 Presence (≥ 5%)

3 (27%)

9 (75%)

/

 Absence (<  5%)

/

3 (25%)

/

 NA

8 (73%)

/

22 (100%)

  1. ADC adenocarcinoma, ctDNA circulating tumor DNA, FFPE formalin-fixed paraffin-embedded, MSS microsatellite stable, MSI microsatellite instability, NA not available