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. 2013 Apr 23;8(4):e61469. doi: 10.1371/journal.pone.0061469

Table 2. Baseline characteristics of the discovery and the validation cohorts.

Variable Discovery cohort n (%) Validation cohort n (%) p-value
Sex
Male 327 (61.50%) 133 (52.78%)
Female 205 (38.50%) 119 (47.22%) p = 0.021
Median age in years (range) 61.4 (20.7–75) 68.7 (25.3–91.6) p<0.001
Histology
non-mucinous 471 (88.50%) 211 (83.73%)
Mucinous 61 (11.50%) 41 (16.27%) p = 0.062
Location
Colon 353 (66.40%) 202 (80.16%)
Rectum 179 (33.60%) 50 (19.84%) p<0.001
Stage
I 99 (18.60%) 48 (19.05%)
II 206 (38.70%) 88 (34.92%)
III 175 (32.90%) 68 (26.98%)
IV 52 (9.80%) 41 (16.27%)
Unknown 7 (2.78%) p = 0.034
Grade
well diff./moderately diff. 489 (91.90%) 211 (83.73%)
poorly diff./undiff. 39 (7.30%) 37 (14.68%)
Unknown 4 (0.80%) 4 (1.59%) p = 0.001
* Invasion
Absence 326 (61.30%) 64 (25.40%)
Presence 166 (31.20%) 101 (40.08%)
Unknown 40 (7.50%) 87 (34.52%) p<0.001
OS status
Dead 177 (33.30%) 155 (61.51%)
Alive 354 (66.60%) 97 (38.49%)
Unknown 1 (0.10%) p<0.001
Median OS follow-up time in years (range) 6.4 (0.4–10.9) 5.4 (0–12.48)
DFS status
Event 208 (39.10%) 167 (66.27%)
no event 323 (60.71%) 85 (33.73%)
Unknown 1 (0.19%) p<0.001
Median DFS follow-up time in years (range) 6 (0.2–10.9) 3.3 (0–12.5)
MSI Status
MSI-H 56 (10.50%) 24 (9.52%)
MSI-L/MSS 455 (85.50%) 228 (90.48%)
Unknown 21 (4%) p = 0.543
Familial risk
Low 256 (48.10%) Na nd
Intermediate/high 276 (59.10%)
BRAF1 Val600Glu mutation
Presence 49 (9.20%) Na nd
Absence 435 (81.80%)
Unknown 48 (9%)
5-FU based treatment
5-FU treated 330 (62.03%) 88 (34.92%)
other/no chemotherapy 199 (37.41%) 148 (58.73%)
Unknown 3 (0.56%) 16 (6.35%) p<0.001
*

Vascular invasion and lymphatic invasion were highly correlated in the discovery cohort (p<0.001). Since data for vascular invasion in the validation cohort was not available, vascular invasion in the discovery cohort and lymphatic invasion in the validation cohort were compared with each other. diff: differentiated, n: number of patients, na: not available, nd: not done.