Table 1.
Characteristics | No. (%) |
---|---|
Age (year) | |
median (range) | 59 (28–88) |
≤59 | 93 (50.3) |
>59 | 92 (49.7) |
Sex | |
male | 97 (52.4) |
female | 88 (47.6) |
Primary site | |
stomach | 87 (47.0) |
small bowel | 88 (47.6) |
large intestine | 8 (4.3) |
others | 2 (1.1) |
Disease status | |
before TKI | 66 (35.7) |
after TKI | 119 (64.3) |
Largest tumor size (mm) | |
≤ 50 | 93 (50.3) |
50–100 | 60 (32.4) |
>100 | 32 (17.3) |
aPrimary mutation | |
KIT exon 9 | 26 (14.1) |
KIT exon 11 | 116 (62.7) |
Others | 12 (6.5) |
Wild type | 20 (10.8) |
NE | 11 (5.9) |
Resection site for PDX | |
primary | 87 (47.0) |
metastasis | 98 (53.0) |
Drug exposure | |
No | 66 (35.7) |
Imatinib alone | 84 (45.4) |
Imatinib and Sunitinib | 25 (13.5) |
Imatinib, Sunitinib, and Regorafenib | 10 (5.4) |
Duration of TKI (months) | |
Imatinib, median (range) | 34.4 (0.9–145.9) |
Sunitinib, median (range) | 11.9 (0.7–58.1) |
Regorafenib, median (range) | 11.1 (3.7–32.9) |
TKI: tyrosine kinase inhibitor.
Wild type: non-KIT and non-PDGFR mutant.
PDX: patient-derived xenograft.
NE: not evaluated.
aMutation analysis in KIT exons 9, 11, 13, 14, and 17, and PDGFRa exons 12 and 18 by Sanger sequencing.