2017
DOI: 10.18632/oncotarget.20816
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Establishment and characterization of patient-derived xenograft models of gastrointestinal stromal tumor resistant to standard tyrosine kinase inhibitors

Abstract: Gastrointestinal stromal tumors (GISTs) with KIT or platelet-derived growth factor receptor alpha (PDGFRa) oncogenic driver gene mutations, respond to tyrosine kinase inhibitors (TKIs) including imatinib, sunitinib, and regorafenib. However, most patients develop TKI resistance; therefore, novel agents are required. We established three TKI-resistant GIST patient-derived xenograft (PDX) models for effective drug development. These were PDX models harboring primary and secondary KIT and additional mutations; KI… Show more

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Cited by 4 publications
(1 citation statement)
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“…Furthermore, a nonsynonymous single‐nucleotide variant, p.T670I , was identified in KIT exon 14 . This variant has been observed in GISTs and, while its prognostic value is unclear, literature suggests that it confers resistance to imatinib mesylate in xenograft model tumors . A previous case report showed resolution of cutaneous GIST metastasis with sunitinib with a KIT exon 11 deletion.…”
Section: Discussionmentioning
confidence: 96%
“…Furthermore, a nonsynonymous single‐nucleotide variant, p.T670I , was identified in KIT exon 14 . This variant has been observed in GISTs and, while its prognostic value is unclear, literature suggests that it confers resistance to imatinib mesylate in xenograft model tumors . A previous case report showed resolution of cutaneous GIST metastasis with sunitinib with a KIT exon 11 deletion.…”
Section: Discussionmentioning
confidence: 96%