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. 2022 Mar 3;10(3):472. doi: 10.3390/healthcare10030472

Table 1.

Clinical Characteristics and Pathologic Features of KRAS-Mutant, KRAS-Wild-Type and Impractical KRAS in Colorectal Cancer Cases.

Characteristic KRAS
Wild-Type
(n = 35)
KRAS
Mutated
(n = 50)
Impractical KRAS
(Not Tested)
(n = 23)
p-Value
Patient characteristics
Age (year) a 71 (63–76) 69 (58–73) 70 (66–76) 0.281 b
Female sex 14 (40.0%) 16 (32.0%) 9 (39.1%) 0.709 c
Primary tumour characteristics
T3 or T4 30 (85.7%) 46 (92.0%) 18 (78.3%) 0.444 c
N1–N2
CRLM characteristics 26 (74.3%) 40 (80.0%) 0 (0%) <0.0001 c
Stage II or III 6 (17.1%) 17 (34.0%) 18 (78.3%) <0.0001 c
Synchronous CRLM 29 (82.9%) 33 (66.0%) 0 (0%) <0.0001 c
Tumour Burden Score a 3.4 (2.1–4.9) 4.0 (2.9–6.2) 3.5 (2.7–5.2) 0.048 b
Tumour number a 2 (1.0–3.0) 2 (1.0–3.3) 1 (1.0–3.0) 0.159 b
Size of largest tumour size (cm) a 2 (1.5–3.6) 2.8 (2.0–5.1) 2.9 (2.2–4.2) 0.040 b
Surgery procedure
Anatomical 12 (34.3%) 28 (56.0%) 9 (39.1%) 0.112 c
Atypical 23 (65.7%) 22 (44.0%) 14 (60.9%)
R1 margin resection status 9 (25.7%) 19 (38.0%) 4 (17.4%) 0.166 c
Chemotherapy
Preoperatively 9 (25.7%) 10 (20.0%) 5 (21.7%) 0.822 c
Postoperatively 21 (60.0%) 33 (66.0%) 6 (26.1%) 0.05 c
Cetuximab preoperatively 0 (0%) 3 (6.0%) 0 (0%) 0.165 c
Cetuximab postoperatively 1 (2.8%) 5 (10.0%) 0 (0%) 0.182 c

CRLM, colorectal liver metastases. a Continuous variables are expressed as median (interquartile range). Categorical variables are expressed as absolute numbers and percentages. b Kruskal–Wallis test, c Chi-square test. Differences in variables were significant at a threshold of p < 0.05.