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Table 1 Clinical characteristics of patients in the training and validation cohort

From: Personalized radiomics signature to screen for KIT-11 mutation genotypes among patients with gastrointestinal stromal tumors: a retrospective multicenter study

 

Total (n = 1143)

Training (n = 617)

Validation (n = 526)

p

Sex, n (%)

   

0.2

Female

536 (46.89)

296 (47.97)

240 (45.63)

 

Male

607 (53.11)

321 (52.03)

286 (54.37)

 

Age, Mean ± SD

61 ± 11.7

61.6 ± 12.2

60.4 ± 11.1

0.075

Location, n (%)

   

0.014

Stomach

756 (66.14)

388 (62.88)

368 (69.96)

 

Non-stomach

387 (33.86)

229 (37.12)

158 (30.04)

 

Mitotic count (/50 HPF), n (%)

   

0.004

 < 5

897 (78.48)

503 (81.52)

394 (74.9)

 

6 ~ 10

146 (12.77)

75 (12.16)

71 (13.5)

 

 > 10

100 (8.75)

39 (6.32)

61 (11.6)

 

Risk of aggressive behavior*, n (%)

   

0.322

Very low

77 (6.74)

49 (7.94)

28 (5.32)

 

Low

481 (42.08)

256 (41.49)

225 (42.78)

 

Intermediate

247 (21.61)

128 (20.75)

119 (22.62)

 

High

338 (29.57)

184 (29.82)

154 (29.28)

 

KIT-11 mutation

   

0.494

No mutation

268 (23.45)

134 (21.72)

134 (25.48)

 

Point mutations or duplications

435 (38.06)

243 (39.38)

192 (36.5)

 

Deletions not involving codons 557/558

197 (17.24)

108 (17.5)

89 (16.92)

 

KIT exon 11 557/558 deletions

243 (21.26)

132 (21.39)

111 (21.1)

 
  1. HPF, high-power field
  2. *According to the modified 2008 National Institute of Health criterion