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. 2015 Mar 30;7(6):6538–6551. doi: 10.18632/oncotarget.3731

Table 1. Clinicopathologic data of nine gastrointestinal stromal tumors.

Patient Sample Tumor location Size (cm) Mitotic rate (per 5 mm2) Risk of progression KIT & PDGFRA mutation Recurrence or metastasis Clinical reponse to imatinib
01 01 stomach 7 2 low wild-type no no treatment
02 02 stomach 6 1 Low wild-type no no treatment
03 03 stomach 6 6 High KIT exon 11 deletion yes Y
04 04 stomach 12 9 High KIT exon 13 missense (K642E) yes Y
05 05 stomach 6 3 low KIT exon 11 missense (V559A) no no treatment
07 07 small intestine (primary) 12 10 high KIT exon 17 missense (N822Y) yes N
08 small intestine (recurrent) 9 7
08 09 small intestine 9 18 high KIT exon 11 deletion yes N
09 10 small intestine 11 8 high KIT exon 9 insertion yes Y

Y, stable disease or partial reponse; N, progressive disease