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. 2013 May 17;8(5):e62951. doi: 10.1371/journal.pone.0062951

Table 2. Patient clinicopathological characteristics.

Clinicopathological feature NO. (%)
Gender male 67 (59)
female 47 (41)
Age (years) <60 72 (50)
≥60 72 (50)
median (years) 59
Gastrointestinal bleeding yes 44 (39)
no 70 (61)
Primary tumor site stomach 73 (65)
duodenum 5 (4)
intestine 24 (21)
colorectum 7 (6)
intraperitoneally with unknown primary origin 5 (4)
Tumor number single 110 (97)
multiple 4 (3)
Primary tumor size >10 cm 31 (27)
5.1–10 cm 44 (39)
0–5 cm 39 (34)
Mitotic index (per 50 HPFs) >10 11 (10)
6–10 20 (18)
0–5 83 (72)
Surrounding tissue invasion yes 24 (21)
no 90 (79)
Tumor necrosis yes 67 (59)
no 47 (41)
Predominant cell type spindle 88 (77)
epithelioid 15 (13)
mixed 11 (10)
Cellularity high 57 (50)
moderate 45 (39)
paucicellular 12 (11)
Postoperative IM treatment yes 21 (18)
no 85 (75)
non-standard* 8 (7)
AFIP-Miettinen criteria very low risk 30 (26)
low risk 23 (20)
moderate risk 16 (14)
high risk 43 (38)
insufficient data 2 (2)
*

8 patients stopped IM treatment at mean of 2.2 months due to severe adverse effects;

one case with double tumors upstaged from low-risk;

two cases with double tumors upstaged from moderate-risk; IM, imatinib mesylate.