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. 2022 Feb 15;54(2):156–168. doi: 10.1038/s12276-022-00731-1

Table 2.

Clinical data of the subgroups classified by the methylation level of the intragenic CpG island of PDX1, EN2, and MSX1; this data includes several patients, age, sex, cancer stage, invasion to adjacent tissues, cancer differentiation levels, microsatellite stability, and the origin of the tumor site.

Parameter Subgroup 1 Subgroup 2 P
N 25 61
Age, mean (range), year 58.2 (40–74) 63.2 (36–83) 0.0343*
Sex (male:female) 13:12 39:22 0.304, ns
Stage n = 25 n = 61
I 0% (0) 1.64% (1) 2.113E-06***
II 8% (2) 0% (0)
III 20% (5) 78.7% (48)
IV 72% (18) 26.2% (12)
Invasion n = 25 n = 61
Lymphatic 56% (14) 45.9% (19) 0.0314*
Vascular 44% (11) 19.6% (8) 0.00172**
Perineural 80% (20) 50.8% (31) 0.0124*
Differentiation n = 24 n = 58
Well 0% (0) 1.7% (1) 0.706, ns
Moderate 91.7% (22) 93.1% (54)
Poor 8.3% (2) 5.2% (3)
Microsatellite n = 23 n = 58
Stable 91.3% (21) 93.1% (54) 0.969, ns
Instable - Low 4.3% (1) 5.2% (3)
Instable - High 4.3% (1) 5.2% (3)
Site of Tumor n = 25 n = 58
Ascending 20% (5) 25.9% (15) 0.667, ns
Descending 4% (1) 0% (0)
Transverse 4% (1) 1.7% (1)
Sigmoid 40% (10) 36.2% (21)
Rectal 16% (4) 20.7% (12)
Rectosigmoid Junction 16% (4) 15.5% (9)

The age of the two subgroups was compared via a two-tailed t test, and the chi-square test was used to analyze the other parameters. Significance levels are presented as ns: nonsignificant, *p < 0.05, **p < 0.01, ***p < 0.001.