RATIONALE: Imatinib mesylate may interfere with the growth of tumor cells and slow the growth of the tumor. PURPOSE: Phase II trial to study the effectiveness of imatinib mesylate in treating patients who have gliomas.
OBJECTIVES: * Determine the therapeutic activity of imatinib mesylate (in terms of objective response and progression-free survival at 6 months) in patients with gliomas. * Determine the safety of this drug in these patients. * Determine the pharmacokinetics of this drug in these patients. OUTLINE: This is a multicenter study. Patients are stratified according to glioma (glioblastoma multiforme vs anaplastic oligodendroglioma or mixed oligoastrocytoma vs anaplastic astrocytoma or recurrent low-grade astrocytoma). Patients receive oral imatinib mesylate once or twice daily. Treatment repeats every 4 weeks for up to 9 courses in the absence of disease progression or unacceptable toxicity. Patients are followed every 2 months for 6 months and then every 3 months thereafter. PROJECTED ACCRUAL: A total of 77 patients (29 patients with glioblastoma multiforme, 24 patients with anaplastic oligodendroglioma or mixed oligoastrocytoma, and 24 patients with anaplastic astrocytoma or recurrent low-grade astrocytoma) will be accrued for this study.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Enrollment
112
Kaiser Franz Josef Hospital
Vienna, Austria
U.Z. Gasthuisberg
Leuven, Belgium
Centre de Lutte Contre le Cancer, Georges-Francois Leclerc
Dijon, France
CRLCC Nantes - Atlantique
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Nantes-Saint Herblain, France
Centre Antoine Lacassagne
Nice, France
Institut Gustave Roussy
Villejuif, France
Azienda Ospedaliera di Padova
Padua, Italy
Daniel Den Hoed Cancer Center at Erasmus Medical Center
Rotterdam, Netherlands
Centre Hospitalier Universitaire Vaudois
Lausanne, Switzerland
Beatson Oncology Centre
Glasgow, Scotland, United Kingdom