Table 3.
MSH2 Deficient CRC | MSH2 Proficient CRC | |||||
---|---|---|---|---|---|---|
Lynch Syndrome (n=46) |
Sporadic MSI (n=15) |
MSS (n=207) |
P value | |||
Clinical | Age | ≥65 | 7 (3) | 80 (12) | 51 (105) | <0.0001 a |
Factor | <65 | 93 (43) | 20 (3) | 49 (102) | <0.0001 b | |
0.0283 c | ||||||
Gender | Female | 33 (15) | 60 (9) | 35 (73) | 0.0372 a | |
Male | 67 (31) | 40 (6) | 65 (134) | 0.864b | ||
0.0553c | ||||||
Location | Proximal | 60 (15) | 92 (12) | 30 (60) | 0.0597a | |
Distal | 40 (10) | 8 (1) | 70 (143) | 0.0022 b | ||
Missing data | (21) | (2) | (4) | <0.0001 c | ||
Genetic | KRAS/BRAF | BRAF mutant | 0 (0) | 67 (10) | 5 (10) | <0.0001 a |
Factor | Mutation | KRAS mutant | 24 (11) | 0 (0) | 35 (73) | 0.0724b |
Status | Both wild type | 76 (35) | 33 (5) | 60 (124) | <0.0001 c | |
Epigenetic | MSH2 | Methylated | 24 (11) | 0 (0) | 0 (0) | 0.0364 a |
Factor | Unmethylated | 76 (35) | 100 (15) | 100 (207) | <0.0001 b | |
1.0c | ||||||
MLH1 | Methylated | 4 (2) | 60 (9) | 0 (0) | <0.0001 a | |
Unmethylated | 96 (44) | 40 (6) | 100 (207) | 0.00259 b | ||
<0.0001 c | ||||||
p16INK4a * | Methylated | 9 (4) | 53 (8) | 16 (33) | 0.000237 a | |
Unmethylated | 91 (40) | 47 (7) | 84 (174) | 0.2444b | ||
0.0003 c | ||||||
p14ARF * | Methylated | 27 (12) | 33 (5) | 8 (16) | 0.6545a | |
Unmethylated | 73 (32) | 67 (10) | 92 (191) | 0.00018 b | ||
0.0011 c | ||||||
MINT1* | Methylated | 34 (15) | 40 (6) | 9 (19) | 0.6798a | |
Unmethylated | 66 (29) | 60 (9) | 91 (188) | <0.0001 b | ||
0.0003 c | ||||||
MINT2* | Methylated | 18 (8) | 53 (8) | 20 (41) | 0.00818a | |
Unmethylated | 82 (36) | 47 (7) | 80 (166) | 0.8049b | ||
0.0025 c | ||||||
MINT31* | Methylated | 48 (21) | 60 (9) | 19 (40) | 0.4116a | |
Unmethylated | 52 (23) | 40 (6) | 81 (167) | <0.0001 b | ||
0.0002 c |
All P values were calculated by the Χ2 test.
P values were calculated between MSH2 deficiency vs. sporadic MSI
P values were calculated between MSH2 deficiency vs. MSS cancers.
P values were calculated between sporadic MSI vs. MSS.
Two cases were not analyzed in MSH2 deficiency cases.