This trial is active, not recruiting.

Condition metastatic renal cell carcinoma
Treatment sunitinib
Phase phase 2
Targets VEGF, FLT-3, KIT, PDGF
Sponsor Asan Medical Center
Collaborator Samsung Medical Center
Start date June 2008
End date September 2011
Trial size 35 participants
Trial identifier NCT01219751, UOSG_AMC_0801


To evaluate the efficacy and safety of sunitinib in non-clear cell type renal cell carcinoma with the exception of pure sarcomatoid carcinoma and collecting duct carcinoma

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Sunitinib 50 mg D1-D28 every 6 weeks
sunitinib Sutene
Sunitinib 50 mg D1-D28 every 6 weeks

Primary Outcomes

Response rate
time frame: up to 12 months

Secondary Outcomes

Progression free survival
time frame: up to 24 months
overall survival
time frame: up to 36 months
time frame: up to 24 months

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: 1. Histologically or cytologically confirmation of renal cell carcinoma without a clear cell histologic component, e.g., papillary type, chromophobe type, or collecting duct type 2. Patients with stage IV or recurrent disease not amenable to surgery, radiotherapy, or combined modality therapy with curative intent. 3. Measurable disease according to RECIST criteria 4. ECOG performance status 1 or better 5. Age 18 years or older 6. Adequate cardiac function 7. Adequate bone marrow, hepatic, and renal function 8. Life expectancy of ≥ 3 months 9. Singed and dated informed consent of document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment Exclusion Criteria: 1. Clear cell type renal cell carcinoma or sarcomatoid carcinoma without any clue to the primary type 2. Diagnosis of any serious secondary malignancy within the last 2 years, except for adequately treated basal cell or squamous cell carcinoma of skin, or in situ carcinoma of cervix uteri 3. Hypertension that cannot be controlled by medications (blood pressure > 150/90 mmHg despite optimal medical therapy) 4. Treatment with anticonvulsant agents and treatment with therapeutic doses of coumadin currently or within 2 weeks prior to first day of sunitinib administration. Low dose coumadin for DVT prophylaxis is permitted (up to 2 mg/day). 5. Pregnancy or breast feeding. 6. Other severe acute or chronic medical or psychiatric condition 7. Prior treatment on sunitinib, sorafenib, or bevacizumab.

Additional Information

Official title Phase II Trial Of Sunitinib In Advanced Non-Clear Cell Type Renal Cell Carcinoma
Description There have been no standard treatment in non-clear cell renal cell carcinoma. Retrospective studies showed sunitinib or sorafenib might be active in non-clear cell renal cell carcinoma, especially papillary type and chromophobe type. This study is to evaluate efficacy and safety of sunitinib in this group of patients.
Trial information was received from ClinicalTrials.gov and was last updated in June 2011.
Information provided to ClinicalTrials.gov by Asan Medical Center.