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. 2021 May 14;11:627460. doi: 10.3389/fonc.2021.627460

Table 1.

Clinicopathological characteristics of patients with MSH2-deficient CRC.

LS Inconclusive dMSH2 x2/t P-value
n = 45 n = 24
No. Percent No. Percent
Age at diagnosis (years)
 Mean (SD) 48.3 (11.3) 53.3 (14.9) 0.120
 ≤70 45 100.0% 20 83.3% - 0.012
 >70 0.0% 4 16.7%
Gender 3.757 0.053
 Male 33 73.3% 12 50.0%
 Female 12 26.7% 12 50.0%
Tumor location 3.202 0.362
 Proximal colon 20 44.4% 13 54.2%
 Distal colon 9 20.0% 4 16.7%
 Rectum 11 24.4% 7 29.2%
 Othera 5 11.1% 0.0%
Tumor stage 3.326 0.505
 I 9 20.0% 4 16.7%
 II 20 44.4% 12 50.0%
 III 8 17.8% 6 25.0%
 IV 5 11.1% 0.0%
 NA 3 6.7% 2 8.3%
Histological type 0.594 0.743
 Adenocarcinoma 41 91.1% 22 91.7%
 Mucinous adenocarcinoma 3 6.7% 2 8.3%
 Otherb 1 2.2% 0.0%
Personal history of cancers 5.269 0.022
 Yes 15 33.3% 2 8.3%
 No 30 66.7% 22 91.7%
Family history of LSRC 11.829 0.003
 Yes 30 66.7% 6 25.0%
 No 15 33.3% 17 70.8%
 Unknown 0.0% 1 4.2%
Revised Bethesda guidelines 2.406 0.121
 Met 40 88.9% 17 70.8%
 Not met 5 11.1% 7 29.2%
 Not available
Amsterdam II criteria 7.134 0.028
 Met 9 20.0% 0.0%
 Not met 36 80.0% 23 95.8%
 Not available 0.0% 1 4.2%

dMSH2, deficient MSH2; LSRC, Lynch syndrome-related cancers; SD, standard deviation.

a. Ungrouped data, including 5 patients with 4 CRC tumors located in two sites among the proximal colon, distal colon or rectum, and 1 colon tumor with an unspecified location.

b. Indicates two synchronous cancers at the sigmoid colon and splenic flexure with mucinous carcinoma and adenocarcinoma histologic types, respectively.