Gastrointestinal stromal tumor: 5 years later Journal Article


Authors: Van Der Zwan, S. M.; DeMatteo, R. P.
Article Title: Gastrointestinal stromal tumor: 5 years later
Abstract: 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 (PDCFRA) 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. © 2005 American Cancer Society.
Keywords: treatment outcome; cancer surgery; gene mutation; clinical feature; clinical trial; pathogenesis; review; placebo; drug efficacy; antineoplastic agents; cancer adjuvant therapy; combined modality therapy; gastrointestinal stromal tumor; imatinib; platelet derived growth factor alpha receptor; stem cell factor; proto oncogene; gastrointestinal stromal tumors; metastasis; pyrimidines; fluorodeoxyglucose f 18; neoplasm metastasis; surgery; protein-tyrosine kinases; cancer epidemiology; piperazines; toxicity; clinical trials; imatinib mesylate; kit gene; gastrointestinal stromal tumor (gist)
Journal Title: Cancer
Volume: 104
Issue: 9
ISSN: 0008-543X
Publisher: Wiley Blackwell  
Date Published: 2005-11-01
Start Page: 1781
End Page: 1788
Language: English
DOI: 10.1002/cncr.21419
PUBMED: 16136600
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 87" - "Export Date: 24 October 2012" - "CODEN: CANCA" - "Source: Scopus"
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  1. Ronald P DeMatteo
    637 DeMatteo