Ontology highlight
ABSTRACT: Importance
Wild-type (WT) gastrointestinal stromal tumors (GISTs), which lack KIT and PDGFRA gene mutations, are the primary form of GIST in children and occasionally occur in adults. They respond poorly to standard targeted therapy. Better molecular and clinical characterization could improve management.Objective
To evaluate the clinical and tumor genomic features of WT GIST.Design, setting, and participants
Patients enrolled in an observational study at the National Institutes of Health starting in 2008 and were evaluated in a GIST clinic held once or twice yearly. Patients provided access to existing medical records and tumor specimens. Self-referred or physician-referred patients younger than 19 years with GIST or 19 years or older with known WT GIST (no mutatio
SUBMITTER: Boikos SA
PROVIDER: S-EPMC5472100 | biostudies-literature | 2016 Jul
REPOSITORIES: biostudies-literature