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. 2015 Apr 20;10(4):e0124899. doi: 10.1371/journal.pone.0124899

Table 1. Characteristics of study populations and tumors.

American cohort Chinese cohort P-value
n = 159 n = 113
Area of recruitment Baltimore, MD Hong Kong, China
Age at enrollment (y)
    Mean (SD) 66.2 (11.3) 55.8 (14.9) P<0.0001
    Range 32–87 32–84
Gender, no. (%) P = 0.0003
    Male 113 (71.1) 56 (49.6)
    Female 46 (28.9) 57 (50.4)
Tumor location a , no. (%) P = 0.0014
    Distal 48 (58.5) 90 (79.6)
    Proximal 34 (41.5) 23 (20.4)
Adenocarcinoma histology, no. (%) NS
    Adenocarcinoma 142 (89.3) 105 (92.9)
    Mucinous adenocarcinoma 16 (10.1) 7 (6.2)
    Adenosquamous 1 (0.6) 0 (0)
    Signet ring cell and mucinous 0 (0) 1 (0.8)
TP53 status b , no. (%) NS
    Wild-type TP53 39 (49.4) 52 (48.2)
    Mutant TP53 40 (50.6) 56 (51.8)
TNM staging c , no. (%) NS
    I 21 (13.3) 9 (8.0)
    II 54 (34.2) 37 (32.7)
    III 65 (41.1) 48 (42.5)
    IV 18 (11.4) 19 (16.8)

a Distal includes tumors located in or distal to the descending colon. Proximal tumors include tumors in or proximal to the splenic flexure. Tumor location was available for all cases in the Chinese cohort and 82 cases in the American cohort.

b TP53 status was evaluated by immunohistochemistry of Formalin-Fixed Paraffin-Embedded (FFPE) tissues. Patients with available data were included.

c For one patient in the American cohort, it was unclear if that patient had stage III or stage IV colon cancer, therefore this patient was removed from analyses stratifying by TNM stage.