OSI-774 and Bevacizumab in the Treatment of Patients With Metastatic Renal Cell Carcinoma
- Registration Number
- NCT00193154
- Lead Sponsor
- SCRI Development Innovations, LLC
- Brief Summary
In this phase II trial, we plan to evaluate the combination of Tarceva and Avastin in the treatment of patients with metastatic renal cell carcinoma. This trial will be one of the first phase II trials to evaluate a combination of targeted agents in the treatment of a common solid tumor with a strong biologic rationale based on Cancer Biology (VHL/HIF/VEGF/EGFr).
- Detailed Description
Upon determination of eligibility, all patients will receive:
Tarceva + Avastin
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 63
To be included in this study, you must meet the following criteria:
- Metastatic or unresectable clear cell kidney cancer confirmed by biopsy
- Previous nephrectomy
- Maximum of 1 previous regimen for metastatic disease
- Ability to perform activities of daily living with minimal assistance
- Measurable disease
- Adequate bone marrow, liver and kidney function
- Give written informed consent prior to study entry
You cannot participate in this study if any of the following apply to you:
- Age < 18 years
- Treatment with more than one previous regimen for metastatic disease
- Clinically significant cardiovascular disease
- Active brain metastases
- History of CNS disease
- Clinical history of coughing or vomiting blood.
- History of thromboembolic disease.
- PEG or G-tube are ineligible.
- Current use of full dose anticoagulants or thrombolytic agents
- Chronic daily treatment with aspirin or NSAIDS
- Any clinical evidence or history of a bleeding or clotting disorder
Please note: There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description OSI-774 & bevacizumab OSI-774 OSI-774 (Tarceva) 150mb PO, days 1-28; bevacizumab (Avastin) 10mg/kg, IV infusion, days 1 and 15; Regimen will be repeated every 28 days. OSI-774 & bevacizumab Bevacizumab OSI-774 (Tarceva) 150mb PO, days 1-28; bevacizumab (Avastin) 10mg/kg, IV infusion, days 1 and 15; Regimen will be repeated every 28 days.
- Primary Outcome Measures
Name Time Method Efficacy of the combination of Tarceva and Avastin 18 months
- Secondary Outcome Measures
Name Time Method Objective response rate 18 months Overall tolerability and toxicity of this combination regimen 18 months Progression-free survival 18 months Overall Survival 18 months
Trial Locations
- Locations (2)
Medical Oncology LLC
🇺🇸Baton Rouge, Louisiana, United States
Grand Rapids Oncology Program
🇺🇸Grand Rapids, Michigan, United States