articleClinical Cancer ResearchJun 1, 2005Closed access

Acquired Resistance to Imatinib in Gastrointestinal Stromal Tumor Occurs Through Secondary Gene Mutation

Memorial Sloan Kettering Cancer Center · Kettering University · +1 more institution

PubMed
Indexed incrossrefpubmed

Abstract

Most gastrointestinal stromal tumors (GIST) have an activating mutation in either KIT or PDGFRA. Imatinib is a selective tyrosine kinase inhibitor and achieves a partial response or stable disease in about 80% of patients with metastatic GIST. It is now clear that some patients with GIST develop resistance to imatinib during chronic therapy. To identify the mechanism of resistance, we studied 31 patients with GIST who were treated with imatinib and then underwent surgical resection. There were 13 patients who were nonresistant to imatinib, 3 with primary resistance, and 15 with acquired resistance after initial benefit from the drug. There were no secondary mutations in KIT or PDGFRA in the nonresistant or…

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Authors

13

Topics & keywords

Keywords
  • Imatinib
  • GiST
  • PDGFRA
  • Medicine
  • Tyrosine-kinase inhibitor
  • Imatinib mesylate
  • Mutation
  • Cancer research
UN Sustainable Development Goals
  • Good health and well-being
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