This phase III trial is designed to assess the difference in progression free survival of two different interleukin-2 regimens for patients with previously untreated metastatic renal cell carcinoma. Interleukin-2 is the FDA approved therapy for metastatic RCCa. When administered by the high-dose bolus method, as it was approved, it needs to be given in an ICU setting due to severe hypotension and other therapy-related complications. Overall, a response rate of 15-20% with a 3-year PFS of 10% is seen. In contrast, out-patient administration of IL-2 by subcutaneous injection has been studied and when administered with out-patient interferon-alpha, is associated with a similar response rate though the 3-yr PFS is somewhat lower. This study is designed to compare these two regimens in a definitive phase III study to determine the specific role of high-dose bolus therapy in this patient population.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000750-27S3
Application #
6265113
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
27
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Type
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
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