| Literature DB >> 26297068 |
Deepa T Patil1, Brian P Rubin2.
Abstract
Approximately 85-90% of adult gastrointestinal stromal tumors (GISTs) harbor KIT and PDGFRA mutations. The remaining cases, including the majority of pediatric GISTs, lack these mutations, and have been designated as KIT/PDGFRA wild-type (WT) GISTs. Nearly 15% of WT GISTs harbor BRAF mutations, while others arise in patients with type I neurofibromatosis. Recent work has confirmed that 20-40% of KIT/PDGFRA WT GISTs show loss of function of succinate dehydrogenase complex. Less than 5% of GISTs lack known molecular alterations ("quadruple-negative" GISTs). Thus, it is important to consider genotyping these tumors to help better define their clinical behavior and therapy.Entities:
Keywords: BRAF; GIST; KIT; PDGFRA; Succinate dehydrogenase
Mesh:
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Year: 2015 PMID: 26297068 DOI: 10.1016/j.path.2015.05.006
Source DB: PubMed Journal: Surg Pathol Clin ISSN: 1875-9157