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Gastrointestinal stromal tumor: 5 years later

There is now considerable interest in gastrointestinal stromal tumor (GIST) because it can be treated effectively with a targeted molecular agent. The majority of GISTs contain an activating mutation in the KIT protooncogene or, occasionally, in the platelet‐derived growth factor‐α (PDGFRA) gene. Fi...

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Bibliographic Details
Published in:Cancer 2005-11, Vol.104 (9), p.1781-1788
Main Authors: van der Zwan, Sanne M., DeMatteo, Ronald P.
Format: Article
Language:English
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Summary:There is now considerable interest in gastrointestinal stromal tumor (GIST) because it can be treated effectively with a targeted molecular agent. The majority of GISTs contain an activating mutation in the KIT protooncogene or, occasionally, in the platelet‐derived growth factor‐α (PDGFRA) gene. Five years ago, imatinib mesylate, a specific molecular inhibitor of the protein products of these 2 genes, was applied to metastatic GIST. Approximately 80% of patients with metastatic GIST benefit from imatinib, although acquired resistance to the agent may develop. For patients with primary GIST, surgery remains the treatment of choice, and whether outcome is improved by adjuvant imatinib is currently under broad investigation. A combination of imatinib therapy and surgery also may be effective in a subset of patients with metastatic or unresectable primary GIST. In this review, the authors summarize the new multimodality approach to GIST. The integration of surgery and molecular therapy in GIST will serve as a prototype for the management of other solid tumors for which targeted agents become available. Cancer 2005. © 2005 American Cancer Society. Gastrointestinal tumor (GIST) has become the prototype disease for the molecular therapy of cancer. Imatinib mesylate was first applied to GIST 5 years ago and since that time has dramatically altered the survival of patients with metastatic disease and may decrease the chance of recurrence after surgical resection of primary disease.
ISSN:0008-543X
1097-0142
DOI:10.1002/cncr.21419