Sorafenib in Treating Patients With Kidney Cancer That Has Spread to the Brain

You may be eligible if

• DISEASE CHARACTERISTICS:
• Histologically or cytologically confirmed renal cell carcinoma metastatic to the brain
• Measurable disease in the brain
• Meets 1 of the following criteria:
• * No prior brain-specific therapy AND no CNS symptoms referable to the brain lesion(s) (with or without concurrent steroid therapy)
• * CNS symptoms referable to the brain lesion(s) AND received primary therapy for the brain lesion(s)
• PATIENT CHARACTERISTICS:
• Blood pressure \< 140/90 mm Hg on 2 separate occasions, taken at least 24 hours apart, within the past 6 weeks (patients on stable anti-hypertensive regimens allowed)
• ECOG performance status (PS) 0-2 OR Karnofsky PS 60-100%
• Bilirubin \< 1.5 times upper limit of normal (ULN)
• ALT/AST \< 2.5 times ULN
• Estimated glomerular filtration rate \> 30 mL/min
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• Able to swallow pills or comply with an oral treatment regimen
• No history of a bleeding diathesis or requirement for full-dose anticoagulation
• No history of allergic reactions attributed to compounds of similar chemical or biologic composition to sorafenib
• No clinical or radiologic evidence of bowel obstruction or perforation
• No other uncontrolled intercurrent illness including, but not limited to, any of the following:
• * Ongoing or active infection
• * Symptomatic congestive heart failure
• * Unstable angina pectoris
• * Cardiac arrhythmia
• * Psychiatric illness or social situation that would limit compliance with study requirements
• PRIOR CONCURRENT THERAPY:
• More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin C) and recovered
• More than 4 weeks since prior radiotherapy to sites outside of the brain and recovered
• More than 8 weeks since prior standard external-beam radiotherapy to the brain unless there is evidence of in-brain progression
• No prior complete surgical resection or radiosurgery of all known brain metastases unless there is evidence of in-brain progression
• No prior sorafenib, sunitinib malate, bevacizumab, or any other agent targeting the platelet-derived growth factor receptor (PDGFR) or vascular endothelial growth factor receptor (VEGFR) kinase cascade
• No other concurrent investigational agents
• No concurrent enzyme-inducing anti-seizure medications, including phenytoin, phenobarbital, carbamazepine, or primidone
• * Concurrent non-enzyme-inducing anti-seizure medications allowed
• No concurrent combination antiretroviral therapy for HIV-positive patients
• No concurrent hematopoietic growth factors except erythropoietin
• No concurrent ketoconazole, itraconazole, or ritonavir
• No concurrent grapefruit juice
• No concurrent Hypericum perforatum (St. John's wort)
• No concurrent chemotherapy
• No concurrent hormonal therapy except steroids for adrenal failure and/or control of CNS edema or hormones for non-disease related conditions (e.g., insulin for diabetes)
• No concurrent palliative radiotherapy
• No other concurrent anticancer therapy
• Concurrent bisphosphonates allowed