Kidney Cancer Clinical Trial
Official title:
Phase II Trial of CC-5013 in Patients With Advanced Renal Cell Carcinoma With Either No Prior Treatment or One Prior Treatment Regimen
Verified date | January 2013 |
Source | Memorial Sloan Kettering Cancer Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
RATIONALE: Biological therapy such as lenalidomide use different ways to stimulate the
immune system and stop tumor cells from growing. It may also stop the growth of tumor cells
by stopping blood flow to the tumor.
PURPOSE: This phase II trial is studying how well lenalidomide works in treating patients
with advanced or unresectable kidney cancer.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | August 2005 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
DISEASE CHARACTERISTICS: - Histologically confirmed renal cell carcinoma (RCC) - Advanced or unresectable disease - At least 1 measurable lesion - No active brain metastases - Prior brain metastases allowed provided patient has been treated with radiotherapy or surgery AND remains asymptomatic for = 6 months PATIENT CHARACTERISTICS: Age - 18 and over Performance status - Karnofsky 70-100% Life expectancy - Not specified Hematopoietic - Absolute neutrophil count = 1,500/mm^3 - Platelet count = 100,000/mm^3 Hepatic - Bilirubin = 1.5 mg/dL - AST and ALT = 2 times upper limit of normal (ULN) (5 times ULN if liver metastases are present) - No hepatitis A, B, or C infection Renal - Creatinine = 2.0 mg/dL Other - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception - HIV negative - No known hypersensitivity to thalidomide - No other serious medical condition, laboratory abnormality, or psychiatric illness that would preclude giving informed consent - No other malignancy within the past 5 years except curatively treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix or breast, localized prostate cancer, or superficial bladder cancer PRIOR CONCURRENT THERAPY: Biologic therapy - No more than 1 prior systemic immunotherapy regimen for RCC - No prior lenalidomide (CC-5013) - No prior or concurrent thalidomide Chemotherapy - No more than 1 prior systemic chemotherapy regimen for RCC Endocrine therapy - No more than 1 prior systemic hormonal therapy regimen for RCC Radiotherapy - See Disease Characteristics - No concurrent radiotherapy Surgery - See Disease Characteristics - At least 4 weeks since prior surgery and recovered Other - No more than 1 other prior systemic therapy regimen for RCC - No other concurrent anticancer therapies - No other concurrent investigational agents |
Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Memorial Sloan-Kettering Cancer Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Memorial Sloan Kettering Cancer Center | National Cancer Institute (NCI) |
United States,
Patel PH, Kondagunta GV, Schwartz L, Ishill N, Bacik J, DeLuca J, Russo P, Motzer RJ. Phase II trial of lenalidomide in patients with metastatic renal cell carcinoma. Invest New Drugs. 2008 Jun;26(3):273-6. Epub 2007 Dec 27. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Efficacy (complete and partial response) | No | ||
Secondary | Toxicity | Yes | ||
Secondary | Adverse events | Yes |
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