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. 2018 Apr 11;16:95. doi: 10.1186/s12967-018-1475-x

Table 2.

Comparative analysis of the clinicopathological findings between wild-type and mutated KRAS groups

Variables KRAS
Wild-type
n = 34 (68.0%)
KRAS
Mutated
n = 16 (32.0%)
Univariate P*
Clinical factors
 Sex
  Male/female 19/15 10/6 0.763
 Age (years) 69 (32 − 81) 69 (47 − 84) 0.303
 CEA (ng/mL) 2.8 (0.4 − 133.1) 4.0 (1.0 − 116.6) 0.163
 CA19-9 (IU/mL) 65.0 (0.8 − 3055.0) 38.7 (0.7 − 766.0) 0.593
 Tumor size (cm)
  Radiographical 4.0 (1.0 − 13.0) 3.0 (1.0 − 14.0) 0.493
Treatment factors
 R0 resection, n (%) 33 (97.1) 15 (93.8) 0.542
 Minor hepatectomy, n (%) 4 (11.8) 2 (12.5) 1.000
 Morbidity
  C-D class III/IV, n (%) 9 (26.5) 3 (18.8) 0.728
 Preoperative chemotherapy
  Present, n (%) 0 0 0
 Adjuvant chemotherapy
  Present, n (%) 22 (64.7) 8 (50.0) 0.366
Pathological factors
 Tumor differentiation
  Well/moderate, n (%) 31 (91.2) 12 (75.0) 0.190
  Poor, n (%) 3 (8.8) 4 (25.0)
 GLUT-1 expression 1.0 (0.0 − 4.0) 4.0 (2.0 − 4.0) < 0.001
 Vascular invasion
  Present, n (%) 22 (64.7) 12 (75.0) 0.533
 Bile duct invasion
  Present, n (%) 16 (47.1) 8 (50.0) 1.000
 Lymph node metastasis
  Present, n (%) 10 (29.4) 5 (31.3) 1.000
 Tumor number
  Multiple, n (%) 6 (17.6) 9 (56.3) 0.008
 Tumor size (cm)
  Pathological 3.6 (1.0 − 13.0) 3.4 (1.0 − 14.0) 0.532
 AJCC stage
  IV, n (%) 16 (47.1) 9 (56.3) 0.762

AJCC American joint committee on cancer/international union against cancer classification, CA 19-9 carbohydrate antigen 19-9, CEA carcinoembryonic antigen, GLUT-1 glucose transporter-1, R0 resection no macroscopic and microscopic tumor remaining, C-D Clavien-Dindo classification system

*Statistically significant differences (P < 0.05) are shown in italic