Kidney Cancer Clinical Trial
Interferon Alfa-2b With or Without Thalidomide in Treating Patients With Metastatic or Unresectable Kidney Cancer
Summary
RATIONALE: Interferon alfa-2b may interfere with the growth of the cancer cells. Thalidomide may stop the growth of cancer by stopping blood flow to the tumor. It is not yet known if interferon alfa-2b is more effective with or without thalidomide in treating kidney cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of interferon alfa-2b with or without thalidomide in treating patients who have previously untreated metastatic or unresectable kidney cancer.
Full Description
OBJECTIVES:
Compare the overall and progression-free survival at 24 weeks in patients with previously untreated metastatic or unresectable renal cell carcinoma treated with interferon alfa-2b with or without thalidomide.
Compare the safety of these 2 regimens in these patients.
Compare the quality of life of patients treated with these 2 regimens.
Compare the pharmacodynamic effects of these regimens on pharmacodynamic measurements of angiogenesis such as serum and plasma angiogenic factor levels in these patients.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to prior nephrectomy (yes vs no), disease-free interval (no more than 1 year vs more than 1 year), and ECOG performance status (0 vs 1 or 2). Patients are randomized to one of two treatment arms.
Arm I: Patients receive interferon alfa-2b subcutaneously (SC) twice daily beginning on day 1.
Arm II: Patients receive interferon alfa-2b as in arm I and oral thalidomide once daily beginning on day 1.
Treatment in both arms continues in the absence of disease progression or unacceptable toxicity. Patients who achieve complete response (CR) continue treatment for 24 weeks past CR.
Quality of life is assessed prior to randomization and then every 4 weeks through week 24.
Patients are followed every 3 months for 2 years and then every 6 months for 3 years.
PROJECTED ACCRUAL: A total of 346 patients (173 per arm) will be accrued for this study within 2 years.
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically proven previously untreated metastatic or unresectable renal cell carcinoma
Retroperitoneal lymph nodes that are unresectable or those that are not resected at the investigator's discretion are considered metastatic disease
Prior nephrectomy allowed provided there is evidence of unresponsive metastatic disease after surgery or within one month prior to study enrollment
Bidimensionally measurable disease
Measurable disease must be outside any prior radiotherapy port
No history of brain metastases unless surgically resected or treated with gamma knife radiotherapy and currently without radiologic evidence of CNS disease
PATIENT CHARACTERISTICS:
Age:
18 and over
Performance status:
ECOG 0-2
Life expectancy:
Not specified
Hematopoietic:
Absolute neutrophil count at least 1,500/mm^3
Hemoglobin at least 9 g/dL (transfusion allowed)
Platelet count at least 100,000/mm^3
Hepatic:
Bilirubin no greater than 1.5 mg/dL
SGOT no greater than 3 times upper limit of normal
Renal:
Creatinine no greater than 1.5 mg/dL OR
Creatinine clearance at least 60 mL/min
Cardiovascular:
No myocardial infarction within the past 6 months
Other:
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use 2 effective methods of contraception (1 highly active method and 1 barrier method) for at least 4 weeks before, during, and for at least 4 weeks after study participation
No other malignancy within the past 5 years except curatively treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix
No uncontrolled diabetes or any other concurrent illnesses that would increase risk
No history of peripheral neuropathy
No severe depression
PRIOR CONCURRENT THERAPY:
Biologic therapy:
No prior immunotherapy (including adjuvant interferon alfa therapy), cellular therapy, or vaccine therapy for renal cell carcinoma
No prior antiangiogenesis therapy for renal cell carcinoma
Immunotherapy for prior malignancy allowed (except for interferon alfa therapy)
Chemotherapy:
No prior chemotherapy for renal cell carcinoma
Chemotherapy for prior malignancy allowed
Endocrine therapy:
No prior hormonal therapy for renal cell carcinoma
Radiotherapy:
See Disease Characteristics
At least 2 weeks since prior radiotherapy and recovered
Surgery:
See Disease Characteristics
Other:
More than 7 days since prior IV antibiotics for infection
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There are 14 Locations for this study
Scottsdale Arizona, 85259, United States
South Bend Indiana, 46601, United States
Des Moines Iowa, 50309, United States
Des Moines Iowa, 50314, United States
Des Moines Iowa, 50316, United States
Papillion Nebraska, 68128, United States
New Brunswick New Jersey, 08903, United States
Albuquerque New Mexico, 87131, United States
Bronx New York, 10466, United States
Hershey Pennsylvania, 17033, United States
Green Bay Wisconsin, 54307, United States
Westmead New South Wales, 2145, Australia
Lima , 34, Peru
San Juan , 00936, Puerto Rico
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