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. 2017 Feb 3;6(3):403–408. doi: 10.3892/mco.2017.1149

Table I.

Clinicopathological factors.

Variables Total (n=93) RAS wild-type (n=44) RAS mutation (n=49) P-value
Age, years (range) 65 (39–83) 68.5 (46–80) 68 (39–83)
Gender 0.101
  Male 56 (60.2) 30 (68.1) 26 (53.0)
  Female 37 (39.8) 14 (31.9) 23 (47.0)
Performance status, n (%) 0.402
  0–1 76 (81.1) 35 (79.5) 41 (83.7)
  2 17 (19.9) 9 (20.1) 8 (16.3)
Tumour-related symptoms, n (%)
  Weight loss >10% 17 (18.3) 10 (22.7) 7 (17.0) 0.143
  Bleeding 30 (32.3) 16 (47.0) 7 (17.0) 0.184
  Occlussion 8 (8.6) 1 (3.0) 14 (34.1) 0.056
Surgery of primary tumour, n (%)
  Yes 49 (52.6) 18 (41.0) 16 (32.6) 0.019a
  No 42 (47.4) 26 (59.0) 33 (67.3)
Location of metastases, n (%)
  Liver 75 (80.6) 38 (86.3) 37 (75.5) 0.145
  Peritoneum 19 (20.4) 10 (22.7) 9 (18.3) 0.396
  Lung 24 (25.8) 7 (15.9) 17 (34.6) 0.033a
  Bone 3 (3.2) 0 (0.0) 3 (6.1) 0.142
  Lymph node 22 (23.7) 10 (22.7) 12 (24.4) 0.519
Number of metastatic locations, n (%)
  1 52 (55.9) 25 (56.8) 27 (20.4) 0.517
  ≥2 48 (44.1) 19 (43.1) 22 (44.9)
Operable metastases after chemotherapy, n (%)
  Yes 17 (19.8) 10 (25.0) 7 (15.2) 0.194
  No 69 (80.0) 30 (75.0) 39 (84.7)
Serum levels, n (%)
  CEA (high) 62 (66.7) 30 (75.0) 32 (76.1) 0.552
  LDH (high) 32 (52.5) 15 (53.5) 17 (51.5) 0.539
  Haemoglobin (low) 22 (28.6) 10 (27.7) 12 (29.2) 0.544
Grade of differentiation, n (%)
  1 12 (12.9) 5 (15.6) 7 (21.2) 0.693
  2 43 (46.2) 22 (68.7) 21 (63.6)
  3 9 (9.7) 5 (15.6) 4 (12.1)
Chemotherapy scheme, n (%)
  FOLFOX/XELOX 58 (62.4) 13 (29.5) 22 (44.8) 0.095
  FOLFOX/XELOX-B 35 (37.6) 31 (70.5) 27 (55.1)
a

Statistically significant differences. CEA, carcinoembryonic antigen; LDH, lactate dehydrogenase.