Pazopanib Hydrochloride in Treating Patients With Metastatic Kidney Cancer (NCT01767636) | Clinical Trial Compass
CompletedPhase 2
Pazopanib Hydrochloride in Treating Patients With Metastatic Kidney Cancer
United States38 participantsStarted 2013-05-16
Plain-language summary
This phase II trial studies how well pazopanib hydrochloride works in treating patients with kidney cancer that has spread to other places in the body (metastatic). Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Pazopanib hydrochloride may also stop the growth of kidney cancer by blocking blood flow to the tumor.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Histological confirmation of non-clear cell renal cancer (including chromophilic \[papillary\], chromophobic, oncocytic, sarcomatoid, collecting duct \[Bellini's duct\]), translocation-type carcinoma or medullary renal cell carcinoma
* Up to one prior treatment for metastatic non clear cell carcinoma is allowed prior to registration as long as the agent used to treat was not pazopanib
* Measurable or non-measurable metastatic disease
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2
* Absolute neutrophil count (ANC) \>= 1500
* Platelets (PLT) \>= 100,000
* Hemoglobin (HgB) \> 9.0 g/dL; NOTE: subjects may not have had a transfusion within 7 days of registration
* Total bilirubin \< 1.5 x upper limit of normal (ULN); NOTE: concomitant elevations in bilirubin above 1.0 x ULN is not permitted
* Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =\< 2.5 x ULN; NOTE: concomitant elevations in ALT/AST above 1.0 x ULN is not permitted
* Urine protein to creatinine ratio (UPC) \< 1; NOTE: if UPC \>= 1, then a 24-hour urine protein must be assessed; subjects must have a 24-hour urine protein value \< 1 g to be eligible
* Prothrombin time (PT) or international normalized ratio (INR) =\< 1.2 x ULN; NOTE: subjects receiving anticoagulant therapy are eligible if their INR is stable and within the recommended range for the desired level of anticoagulation
* A female is eligible to enter and participate in this study if she …