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. 2017 Apr 4;8(21):35165–35175. doi: 10.18632/oncotarget.16815

Table 1. Clinicopathologic and molecular characteristics in 84 colorectal MACs with and without SAC morphology.

Characteristic MAC withoutSAC morphology(n=52)a MAC with SACmorphology(n=32)b P-value
Gender 0.255
 Male 31 (59.6) 15 (46.9)
 Female 21 (40.4) 17 (53.1)
Age 0.157
 ≤ 70 years 31 (59.6) 14 (43.8)
 > 70 years 21 (40.4) 18 (56.3)
Location 0.001
 Proximal colon 18 (34.6) 23 (71.9)
 Distal colon or rectum 34 (65.4) 9 (28.1)
Differentiation 0.952
 Well 9 (17.3) 5 (15.6)
 Moderate 36 (69.2) 22 (68.8)
 Poor 7 (13.5) 5 (15.6)
AJCC TNM stage 0.889
 Stage I 2 (3.8) 1 (3.1)
 Stage II 22 (42.3) 14 (43.8)
 Stage III 21 (40.4) 11 (34.4)
 Stage IV 7 (13.5) 6 (18.8)
KRAS mutation (n=75) 19 (42.2) 13 (43.3) 0.924
BRAF mutation (n=73) 3 (7) 8 (26.7) 0.042
CIMP positive (n=77) 3 (6.5) 8 (25.8) 0.023
Defective mismatch repair protein 12 (23.1) 7 (21.9) 0.898

AJCC, American Joint Committee on Cancer; CIMP, CpG island methylator phenotype; MAC, mucinous adenocarcinoma; SAC, serrated adenocarcinoma.

a Values are calculated for 52 MACs without SAC morphology unless specified otherwise, and are presented as number and percentage of patients.

b Values are calculated for 32 MACs with SAC morphology unless specified otherwise, and are presented as number and percentage of patients.