Imatinib for the treatment of patients with unresectable or metastatic malignant KIT-positive gastrointestinal stromal tumours :: an open-label Belgian trial

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作者
Prenen, Hans
Dumez, Herlinde
Stefan, Cristiana
Hoeben, Ann
Wouters, Carine
Van Lierde, Marie-Anne
Sciot, Raf
van Oosterom, Allan T.
Peeters, Marc
Polus, Marc
Duck, Lionel
Gil, Thierry
Schoffski, Patrick
机构
[1] Katholieke Univ Leuven, Dept Gen Med Oncol, Leuven Canc Inst, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Dept Pathol, B-3000 Louvain, Belgium
[3] Ghent Univ Hosp, Dept Gastroenterol, B-9000 Ghent, Belgium
[4] Liege Univ Hosp, Dept Gastroenterol, Liege, Belgium
[5] Clin St Pierre, Dept Hematol & Oncol, Ottignies, Belgium
[6] Inst Jules Bordet, B-1000 Brussels, Belgium
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R57 [消化系及腹部疾病];
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摘要
Background: Gastrointestinal stromal tumours (GIST) are the most common mesenchymal tumours of the gastrointestinal tract. They are defined immunohistologically as KIT positive tumours. The only effective treatment for malignant GIST was surgery until 2000. Imatinib mesylate (STI571, Glivec (R)) has shown substantial anticancer activity in patients with metastatic or unresectable GIST. Patients and methods : 57 patients who were diagnosed with unresectable or metastatic malignant GIST were entered into this study. The patients were given 400 mg Glivec orally once daily. The dose could be increased to 600 mg orally once daily and then to 400 mg twice daily if tumour progression was noticed. Daily treatment was interrupted or dose was decreased only in the case of limiting toxicities. We evaluated the tumour response and the safety of the drug. Results : 85% of GIST patients showed a partial response or stable disease after 8 weeks of treatment with imatinib. The main side effects were nausea, vomiting, anorexia, skin rash, periorbital oedema and diarrhea. Conclusion : This study confirms that imatinib is an active agent against malignant GIST with manageable toxicities.
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页码:367 / 371
页数:5
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