Sorafenib and Interferon Alfa in Treating Patients With Locally Advanced or Metastatic Kidney Cancer

• Status: Terminated
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for their growth or by blocking blood flow to the tumor. Interferon alfa may interfere with the growth of tumor cells and slow the growth of kidney cancer. Sorafenib may help interferon alfa kill more tumor cells by making tumor cells more sensitive to the drug. Giving sorafenib together with interferon alfa may kill more tumor cells. This phase II trial is studying how well giving sorafenib with interferon alfa works in treating patients with locally advanced or metastatic kidney cancer.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Cancer Institute (NCI)
• Treatments: Interferon alpha-2; Interferon-alpha; Interferons; Niacinamide; Sorafenib

Criteria

Inclusion Criteria:

• Histologically or cytologically confirmed renal cell carcinoma

• Locally advanced or metastatic disease

• All histologic subtypes allowed

• Measurable disease

• At least 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral CT scan

• No known brain metastases or leptomeningeal disease

• Performance status - ECOG 0-2

• WBC ≥ 3,000/mm^3

• Absolute neutrophil count ≥ 1,500/mm^3

• Platelet count ≥ 100,000/mm^3

• No bleeding diathesis

• Bilirubin normal

• AST and ALT ≤ 2.5 times upper limit of normal (ULN)

• Creatinine ≤ 1.5 times ULN

• Creatinine clearance ≥ 60 mL/min

• No uncontrolled hypertension

• No symptomatic congestive heart failure

• No unstable angina pectoris

• No cardiac arrhythmia

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No history of sensitivity to E. coli-derived products

• No history of severe depression

• No active infection requiring antibiotics

• No seizure disorder requiring antiepileptic medication

• No medical condition likely to require systemic corticosteroids

• No autoimmune disorder that could result in life-threatening complications

• No other uncontrolled illness

• No psychiatric illness or social situation that would preclude study compliance

• No more than 1 prior biologic response modifier regimen

• At least 4 weeks since prior biologic response modifiers

• No prior interferon alfa

• No prior chemotherapy

• At least 4 weeks since prior radiotherapy to non-index lesions

• Prior radiotherapy to index lesion allowed provided irradiated lesion progressed ≥ 20% in diameter

• At least 2 weeks since prior major surgery

• No concurrent combination antiretroviral therapy for HIV-positive patients

• No concurrent therapeutic anticoagulation therapy

• Concurrent prophylactic anticoagulation, such as low-dose warfarin, for venous or arterial access device allowed provided PT, PTT, and INR are normal

• No other concurrent investigational agents

• No other concurrent anticancer therapy