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Table 2 Demographic and clinicopathologic data between two groups

From: Synchronous gastrointestinal cancer and gastrointestinal stromal tumors: a single-institution experience

Variables

Synchronous group (n = 47, %)

Non-synchronous group (n = 239, %)

P value

Age, years

66.4 ± 5.6

61.2 ± 4.2

0.231

Gender

  

0.614

 Male

29 (61.7)

138 (57.7)

 

 Female

18 (38.3)

101 (42.3)

 

ECOG score

  

<0.001

 ≤ 1

16 (34.0)

174 (72.8)

 

 ≥ 2

31 (66.0)

65 (27.2)

 

Tumor site

  

0.028

 Stomach

43 (91.5)

176 (73.6)

 

 Small intestine

3 (6.4)

48 (20.1)

 

 Othersa

1 (2.1)

15 (6.3)

 

Tumor size, cm

1.6 ± 0.4

5.9 ± 3.5

<0.001

 Median (range, cm)

0.7 (0.2~2.5)

5.25 (1.5~30.0)

 

Mitotic count (50 HPF)

  

0.011

 ≥ 10

0 (0.0)

27 (11.3)

 

 < 10

47 (100.0)

212 (88.7

 

NIH risk classification

  

<0.001

 Very low and low

42 (89.4)

76 (31.8)

 

 Intermediate and high

5 (10.6)

163 (68.2)

 

IM adjuvant treatment

  

<0.001

 Yes

2 (4.3)

139 (58.2)

 

 No

45 (95.7)

100 (41.8)

 

Synchronous cancer

   

 Esophageal carcinoma

12 (25.5)

 

 Gastric carcinoma

27 (57.4)

 

 Pancreatic adenocarcinoma

1 (2.1)

 

 Colorectal carcinoma

7 (14.9)

 

Hospital stay, days

18.6 ± 5.3

16.9 ± 4.2

0.209

  1. ECOG Eastern Cooperative Oncology Group, HPF high power field, NIH National Institutes of Health, IM imatinib mesylate
  2. aIncluding omentum, retroperitoneal, mesentery of large and small intestine, and pelvic mass