Kidney Cancer Clinical Trial

Bevacizumab and Interleukin-2 in Treating Patients With Metastatic Kidney Cancer

Summary

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Interleukin-2 may stimulate the white blood cells to kill tumor cells. Giving bevacizumab together with interleukin-2 may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving bevacizumab together with interleukin-2 works in treating patients with metastatic kidney cancer.

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Full Description

OBJECTIVES:

Primary

Estimate the response, progression-free survival, and overall survival of patients with metastatic renal cell carcinoma (RCC) treated with bevacizumab and high-dose interleukin-2 (IL-2).

Secondary

Compare the response and survival of patients with metastatic RCC treated with bevacizumab and high-dose IL-2 with the historical data of patients treated with high-dose IL-2 alone.
Compare the toxicity of bevacizumab and high-dose IL-2 in patients with metastatic RCC with the historical data of patients treated with high-dose IL-2 alone, in terms of number of doses of IL-2 administered during the first course of therapy, toxicity after the scheduled ninth dose of IL-2, and frequency of grade III and IV or unexpected or rare toxicities.
Compare the time to disease progression in patients with metastatic RCC treated with bevacizumab and high-dose IL-2 with the historical data of patients treated with high-dose IL-2 alone.
Evaluate the pharmacokinetics and pharmacodynamics of bevacizumab and high-dose IL-2 during course 1.
Correlate serum vascular endothelial growth factor (VEGF) levels, DC function, TCR zeta chain expression, and arginase or arginine levels with toxicity, response, and survival of patients treated with this regimen.
Evaluate the utility of known prognostic criteria for RCC patients on clinical outcome.

OUTLINE: This is a multicenter study. Patients are stratified according to prognosis (good vs intermediate vs poor).

Patients receive bevacizumab IV over 30-90 minutes on days -13, 1, 15, 29, 43, 57, and 71 during course 1 and on days 1, 15, 29, 43, 57, and 71 during courses 2 and 3. Patients also receive high-dose interleukin-2 every 8 hours on days 1-5 and 15-19. Treatment repeats every 84 days for up to 3 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3 months for 2 years and then every 6 months thereafter.

PROJECTED ACCRUAL: A total of 65 patients will be accrued for this study.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Histologically confirmed metastatic renal cell carcinoma (RCC) with predominantly clear cell histology
Measurable disease
No history of tumor-related hemorrhage
No history of CNS or brain metastases

PATIENT CHARACTERISTICS:

Karnofsky performance status ≥ 80%
Absolute neutrophil count ≥ 1,000/mm^3
Platelet count ≥ 100,000/mm^3
Hemoglobin ≥ 9 g/dL (transfusion or recombinant erythropoietin growth factors allowed)
AST ≤ 2 times upper limit of normal (ULN) (5 times ULN if due to liver metastases)
Serum total bilirubin ≤ 2 times ULN (except for patients with Gilbert's disease)
Serum creatinine ≤ 1.5 mg/dL OR creatinine clearance ≥ 60 mL/min

FEV_1 ≥ 2.0 L or ≥ 75% of predicted

Pulmonary function testing required for patients over age 50 or with significant pulmonary or smoking history
No history of cerebrovascular accident or transient ischemic attacks

No evidence of any of the following cardiac conditions*:

Congestive heart failure
Symptoms of coronary artery disease
Myocardial infarction < 6 months prior to study entry
Serious cardiac arrhythmias
Unstable angina NOTE: *Patients > 40 years old or who have had a previous myocardial infarction > 6 months prior to study entry are required to have a negative or low probability cardiac stress test for cardiac ischemia
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception

No other malignancy within the past 5 years except nonmelanoma skin cancer or noninvasive cancer, such as cervical carcinoma in situ, superficial bladder cancer without local recurrence, or breast cancer in situ

Patients with a history of another invasive malignancy must be in complete remission for ≥ 5 years
No positive serology for HIV, hepatitis B, or hepatitis C
No significant co-morbid illness, such as uncontrolled diabetes or active infection, that would preclude study treatment

No history of inflammatory bowel disease or other serious autoimmune disease

Thyroiditis or rheumatoid arthritis allowed
No uncontrolled hypertension (i.e., blood pressure > 150/100 mm Hg)
Proteinuria ≤ 3+ by dipstick OR proteinuria < 2 gm by 24-hour urine collection
Urine protein:creatinine ration < 1.0
No abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to study entry
No significant traumatic injury within the past 28 days
No serious, nonhealing wound, ulcer, or bone fracture
No active bleeding
No history of other serious hemorrhage, bleeding diathesis, or underlying coagulopathy
No history of deep venous thrombosis, clinically significant peripheral vascular disease, or other thrombotic event

PRIOR CONCURRENT THERAPY:

No organ allografts
At least 4 weeks since prior radiotherapy or surgery and recovered
No prior systemic therapy for metastatic RCC
No prior bevacizumab or interleukin-2
At least 2 weeks since prior steroids
No major surgery or open biopsy within the past 28 days
No minor surgical procedures, fine needle aspirations, or core biopsies within the past 7 days, except central venous catheter placement
No concurrent major surgery
No concurrent corticosteroids or other immunosuppressants

Study is for people with:

Kidney Cancer

Phase:

Phase 2

Estimated Enrollment:

65

Study ID:

NCT00301990

Recruitment Status:

Unknown status

Sponsor:

Jonsson Comprehensive Cancer Center

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There are 11 Locations for this study

See Locations Near You

Jonsson Comprehensive Cancer Center at UCLA
Los Angeles California, 90095, United States More Info
Clinical Trials Office - Jonsson Comprehensive Cancer Center a
Contact
888-798-0719
Cardinal Bernardin Cancer Center at Loyola University Medical Center
Maywood Illinois, 60153, United States More Info
Clinical Trials Office - Cardinal Bernardin Cancer Center
Contact
708-226-4357
Indiana University Melvin and Bren Simon Cancer Center
Indianapolis Indiana, 46202, United States More Info
Clinical Trials Office - Indiana University Cancer Center
Contact
317-274-2552
Beth Israel Deaconess Medical Center
Boston Massachusetts, 02215, United States More Info
Clinical Trials Office - Beth Israel Deaconess Medical Center
Contact
617-667-9925
Barbara Ann Karmanos Cancer Institute
Detroit Michigan, 48201, United States More Info
Clinical Trials Office - Barbara Ann Karmanos Cancer Institute
Contact
313-576-9363
Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center
Lebanon New Hampshire, 03756, United States More Info
Clinical Trials Office - Norris Cotton Cancer Center
Contact
603-650-7609
[email protected]
Our Lady of Mercy Medical Center Comprehensive Cancer Center
Bronx New York, 10466, United States More Info
Janice P. Dutcher, MD
Contact
718-304-7200
Providence Cancer Center at Providence Portland Medical Center
Portland Oregon, 97213, United States More Info
Clinical Trials Office - Providence Cancer Center at Providenc
Contact
503-215-6412
UPMC Cancer Centers
Pittsburgh Pennsylvania, 15232, United States More Info
Clinical Trials Office - UPMC Cancer Centers
Contact
412-647-8073
Vanderbilt-Ingram Cancer Center
Nashville Tennessee, 37232, United States More Info
Clinical Trials Office - Vanderbilt-Ingram Cancer Center
Contact
800-811-8480
University of Virginia Cancer Center
Charlottesville Virginia, 22908, United States More Info
Geoffrey R. Weiss, MD
Contact
434-243-0066
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Kidney Cancer

Phase:

Phase 2

Estimated Enrollment:

65

Study ID:

NCT00301990

Recruitment Status:

Unknown status

Sponsor:


Jonsson Comprehensive Cancer Center

How clear is this clinincal trial information?

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