4.5 Review Book Chapter

Molecular pathobiology of gastrointestinal stromal sarcomas

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ANNUAL REVIEWS
DOI: 10.1146/annurev.pathmechdis.3.121806.151538

Keywords

gist; imatinib; tyrosine kinase inhibitor; sunitinib

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Gastrointestinal stromal tumors (GISTs) form,ill interesting group of sarcomas whose unique pathobiology provides a model of how molecularly targeted therapeutics call have a major impact on patient welfare. Approximately 85% of GISTs are driven by oncogenic mutations in either of two receptor tyrosine kinases:KIT or platelet-derived growth factor receptor cc. We review the pivotal relationship between specific mutations ill these kinase genes, the origin and pathologic spectrum of GISTs, and the response of these tumors to treatment with kinase inhibitors such as imatinib and sunitinib. Mechanisms of resistance to kinase inhibitor therapy are discussed, and targets for the next generation of therapeutics are considered. The rapid evolution ill Our understanding of GISTs, which sterns directly from the close alliance of basic and clinical researchers ill the field, illustrates the growing role of the molecular classification of solid tumors in the development of modern oncological treatments.

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