Metastatic Cancer
Conditions
Keywords
tumors metastatic to brain
Brief summary
RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as RSR13 may make tumor cells more sensitive to radiation therapy. PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy to the brain with or without RSR13 in treating patients who have brain metastases.
Detailed description
OBJECTIVES: * Compare the median survival time in patients with brain metastases after receiving treatment with whole brain radiotherapy with or without RSR13. * Compare the response rate to these treatment regimens in these patients. * Compare the time to progression after receiving these treatment regimens in these patients. * Compare quality of life in these patients receiving these treatment regimens. * Compare cause of death (neurologic vs nonneurologic death) in these patients after receiving these treatment regimens. * Determine the safety of RSR13 in these patients. * Assess the pharmacokinetics of RSR13 in these patients. OUTLINE: This is a randomized, open label, comparative, multicenter study. Patients are stratified according to the Radiation Therapy Oncology Group RPA Class (I vs II). Patients are further stratified within the RPA class II stratum according to site of primary cancer (non-small cell lung cancer vs breast vs other). Patients are randomized to one of two treatment arms. * Arm I: Patients receive whole brain radiotherapy 5 days a week for two weeks in conjunction with supplemental oxygen breathing. * Arm II: Patients receive RSR13 IV over 30 minutes followed by whole brain radiotherapy and supplemental oxygen breathing as in arm I. Quality of life is assessed at the first and last day of radiotherapy, at 1 month, 3 months, and then every 3 months until disease progression. Patients are followed at 1 month, 3 months, every 3 months until disease progression, and then for survival. PROJECTED ACCRUAL: A maximum of 408 (204 per treatment arm) patients will be accrued for this study.
Interventions
DRUGefaproxiral
RADIATIONradiation therapy
Sponsors
Spectrum Pharmaceuticals, Inc
Study design
Allocation
RANDOMIZED
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Radiographically, histologically, or cytologically confirmed brain metastases with histologically or cytologically confirmed primary malignancy except the following: * Small cell lung cancer, germ cell tumors, and lymphomas * No leptomeningeal metastases PATIENT CHARACTERISTICS: Age: * 18 and over Performance status: * Karnofsky 70-100% Life expectancy: * Not specified Hematopoietic: * Hemoglobin at least 10 g/dL * WBC at least 2,000/mm3 * Platelet count at least 75,000/mm3 Hepatic: * Bilirubin no greater than 2.0 mg/dL * ALT and AST no greater than 3 times upper limit of normal Renal: * Creatinine no greater than 2.0 mg/dL Pulmonary: * Forced vital capacity and forced expiratory volume at least 50% of normal in patients with significant intrathoracic tumor involvement, chronic obstructive pulmonary disease, interstitial lung disease, or pulmonary embolism * Resting and exercise oxygen saturation at least 90% on room air Other: * No other concurrent active malignancy from a second histologic site * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior biologic therapy or immunotherapy for brain metastases * At least 28 days since prior investigational biologic therapy Chemotherapy: * No prior chemotherapy for brain metastases * No chemotherapy for brain metastases for at least one month following radiation therapy * At least 7 days since prior chemotherapy for primary tumor or extracranial metastases * No planned chemotherapy during radiation therapy Endocrine therapy: * No prior hormonal therapy for brain metastases * Prior or concurrent corticosteroid therapy allowed Radiotherapy: * No prior whole brain radiotherapy for brain metastases * No prior stereotactic radiosurgery for brain metastases Surgery: * Prior surgery allowed for brain metastases if at least one measurable lesion remains Other: * At least 28 days since prior investigational drug or device * No prior RSR13
Countries
Australia, Belgium, Canada, France, Germany, Hungary, Italy, United Kingdom, United States
Outcome results
None listed