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Clinical Trial Summary

RATIONALE: Pazopanib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase II trial is studying how well pazopanib hydrochloride works in treating patients with stage IV kidney cancer.


Clinical Trial Description

PRIMARY OBJECTIVES: I. To determine the response rate (RR) associated with pazopanib (pazopanib hydrochloride) as 3rd-line therapy in metastatic renal cell carcinoma (mRCC) patients who have failed therapy with a distinct vascular endothelial growth factor (VEGF)-tyrosine kinase inhibitor (TKI). SECONDARY OBJECTIVES: I. To determine if baseline hepatocyte growth factor (HGF), endothelial selectin (E-selectin) and interleukin-6 (IL-6) are associated with progression-free survival (PFS). II. To determine if pre-metastatic niche density in regional lymph nodes (LNs) is associated with PFS. III. To determine an association between E-selectin, IL-6 and pre-metastatic niche density. IV. To evaluate the prognostic effect of pre-metastatic niches as an independent factor in time to first relapse. V. To determine if phosphorylated signal transducer and activator of transcription 3 (pSTAT3) in tumor tissue is associated with PFS. VI. To describe the toxicity associated with pazopanib in this patient population. VII. To evaluate PFS and overall survival (OS). VIII. To compare, within patient, time to tumor progression of 2nd-line therapy with time to tumor progression on pazopanib as 3rd-line therapy. OUTLINE: Patients receive oral pazopanib hydrochloride once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 6 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01157091
Study type Interventional
Source City of Hope Medical Center
Contact
Status Completed
Phase Phase 2
Start date December 8, 2010
Completion date December 31, 2013

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