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Molecular subtypes of gastrointestinal stromal tumors and their prognostic and therapeutic implications
Author(s) -
Zoltán Szűcs,
Khin Thway,
Cyril Fisher,
Ramesh Bulusu,
Anastasia Constantinidou,
Charlotte Benson,
Winette T.A. van der Graaf,
Robin L. Jones
Publication year - 2016
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon-2016-0192
Subject(s) - pdgfra , gist , medicine , stromal cell , imatinib , oncology , clinical significance , acquired resistance , imatinib mesylate , stromal tumor , bioinformatics , cancer , biology , myeloid leukemia
Gastrointestinal stromal tumors (GISTs) are composed of various molecular subtypes, with differing prognostic and predictive relevance. Previously, tumors lacking mutations in the KIT and PDGFRA genes have been designated as 'wild-type' GISTs; however, they represent a heterogeneous group currently undergoing further subclassification. Primary and secondary resistance to imatinib poses a significant clinical challenge, therefore ongoing research is trying to evaluate mechanisms to overcome resistance. Thorough understanding of the prognostic and predictive relevance of different genetic subtypes of GIST can guide clinical decision-making both in the adjuvant and the metastatic setting. Further work is required to identify tailored therapies for specific subgroups of GISTs wild-type for KIT and PDGFRA mutations and to identify predictive factors of resistance to currently approved systemic therapies.

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