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Cited by 1,369

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Adjuvant imatinib mesylate after resection of localised, primary gastrointestinal stromal tumour: a randomised, double-blind, placebo-controlled trial

Open access
DeMatteo, Ronald P, Ballman, Karla V, Antonescu, Cristina R, Maki, Robert G, Pisters, Peter WT, Demetri, George D, Blackstein, Martin E, Blanke, Charles D, von Mehren, Margaret, Brennan, Murray F, Patel, Shreyaskumar, McCarter, Martin D, Polikoff, Jonathan A, Tan, Benjamin R, Owzar, Kouros·2009·The Lancet

Abstract

Background Gastrointestinal stromal tumor (GIST) is the most common sarcoma of the intestinal tract. The standard treatment of localized, primary GIST has been surgical resection alone. Most GISTs have a mutation in the KIT proto-oncogene, or less commonly in platelet-derived growth factor receptor alpha (PDGFRα). Imatinib mesylate is a small molecule that inhibits activation of the KIT and PDGFRα proteins and is effective in metastatic GIST. We hypothesized that adjuvant treatment with imatinib would result in improved recurrence-free survival (RFS) compared to placebo treatment following resection of localized, primary GIST. Methods We performed a randomized phase 3, double-blind, placebo-controlled, multicenter trial. Eligible patients had complete gross resection of a primary GIST at least 3 cm in size that stained positive for KIT protein. Patients were randomly assigned to receive imatinib 400 mg/day or placebo daily for one year following surgical resection. Patients assigned to placebo were eligible to crossover to imatinib treatment in the event of tumor recurrence. The primary endpoint was RFS and intention to treat analysis was performed. This study is registered at ClinicalTrials.gov, number NCT00041197. Findings From July 2002 to April 2007, 359 patients were randomized to imatinib and 354 to placebo. Accrual was stopped early based on the results of a planned interim analysis. Imatinib significantly prolonged RFS compared with placebo (98% vs. 83% at 1 year; overall hazard ratio 0.35; one-sided p<0.0001). Overall survival (OS) was similar (99.2% vs. 99.7% at 1 year; hazard ratio 0.66; p=0.47). Adjuvant imatinib was well-tolerated with a low rate of serious adverse events. Interpretation Adjuvant imatinib therapy is safe and compared to placebo treatment appears to prolong RFS following the resection of primary GIST. OS is not different at this time.

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Metadata

Authors
DeMatteo, R. P., Ballman, K. V., Antonescu, C. R., Maki, R. G., Pisters, P. W., Demetri, G. D., Blackstein, M. E., Blanke, C. D., von Mehren, M., Brennan, M. F., Patel, S., McCarter, M. D., Polikoff, J. A., Tan, B. R., & Owzar, K.
Venue
The Lancet
Publisher
Elsevier BV
Published
2009-03
Volume
373
Issue
9669
Pages
1097-1104
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
OpenAlex
W2165837347
Cited by
1,369
References
1
FWCI
118.51
Type
journal article
Language
en
Open access
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CoChat. (2026). Citation check: Adjuvant imatinib mesylate after resection of localised, primary gastrointestinal stromal tumour: a randomised, double-blind, placebo-controlled trial. https://app.cochat.ai/papers/10.1016/s0140-6736(09)60500-6
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DeMatteo, R. P., Ballman, K. V., Antonescu, C. R., Maki, R. G., Pisters, P. W., Demetri, G. D., Blackstein, M. E., Blanke, C. D., von Mehren, M., Brennan, M. F., Patel, S., McCarter, M. D., Polikoff, J. A., Tan, B. R., & Owzar, K. (2009). Adjuvant imatinib mesylate after resection of localised, primary gastrointestinal stromal tumour: a randomised, double-blind, placebo-controlled trial. The Lancet. https://doi.org/10.1016/s0140-6736(09)60500-6

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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