RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Indinavir and ritonavir may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether external-beam radiation therapy is more effective with or without indinavir and ritonavir in treating patients with brain metastases. PURPOSE: This randomized phase II trial is studying external-beam radiation therapy alone to see how well it works compared to external-beam radiation therapy given together with indinavir and ritonavir in treating patients with brain metastases.
OBJECTIVES: * Compare the efficacy, in terms of time to treatment failure at CNS level and 4-months treatment failure rate, in patients with brain metastases treated with external-beam radiotherapy in combination with indinavir sulfate and ritonavir versus external-beam radiotherapy alone. * Prospectively investigate the efficacy of a potentially antiangiogenic agent, indinavir sulfate. * Investigate the antineoplastic activity of indinavir sulfate in combination with ionizing radiation in cancer patients with metastatic disease to the brain. OUTLINE: Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo radiotherapy to the brain once daily, 5 days a week for 2 weeks (10 doses total). Patients also receive oral indinavir sulfate and oral ritonavir twice daily for 35 days beginning at day 1 of radiotherapy. * Arm II: Patients undergo radiotherapy to the brain once daily, 5 days a week for 2 weeks (10 doses total). Patients complete quality of life questionnaires, including QOL-30 and the Mini Mental Status Examination, at baseline, 2 weeks after completion of radiotherapy, and at 1 and 3 months after completion of study treatment. After completion of study treatment, patients are followed periodically for at least 4 months.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Enrollment
60
Hopital Cantonal Universitaire de Geneve
Geneva, Switzerland
RECRUITINGOncology Institute of Southern Switzerland - Lugano
Lugano, Switzerland
RECRUITINGUniversitaetsSpital Zuerich
Zurich, Switzerland
RECRUITINGTime to treatment failure in the brain (TTF) as determined by the radiological response rate
Overall survival (OS)
Radiological volumetric response to treatment
Local intracranial disease progression at 4 months
Progression-free survival at 6 months
Improvement of symptoms
Time to symptom relapse or symptom progression
Duration of use of steroids
Duration of use of anticonvulsive drugs
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