Breast Cancer Clinical Trial
Official title:
A Phase 2 Study of GW786034 (Pazopanib) in Patients With Recurrent and/or Metastatic Invasive Breast Carcinoma
This phase II trial is studying how well giving pazopanib works in treating patients with recurrent or metastatic invasive breast cancer. Pazopanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.
PRIMARY OBJECTIVE:
I. To determine the antitumor activity of pazopanib, in terms of objective response rate
(partial and complete response), in patients with recurrent or metastatic invasive breast
cancer.
SECONDARY OBJECTIVES:
I. To determine the duration of objective response, rate and duration of stable disease.
II. To determine 6-month progression-free and median and overall survival rates in patients
treated with this drug.
III. To document the safety and tolerability of this drug in these patients.
OUTLINE: This is a multicenter, open label study.
Patients receive oral pazopanib once daily on days 1-28. Courses repeat every 28 days in the
absence of disease progression or unacceptable toxicity. Blood samples are collected at
baseline and at 1, 4, and 8 weeks for correlative laboratory studies. Blood samples are
evaluated for the following tumor markers by ELISA: VEGF, bFGF, sFLT-1, sTIE-2, sE-Selectin,
VCAM-1, PDGF-AA, PDGF-AB and PDGF-BB. TSP-1 in plasma is measured by Accucyte™ competitive
immunoassay.
After completion of study treatment, patients are followed every 3 months.
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