Advanced Adult Primary Liver Cancer Clinical Trial
Official title:
A Phase II Study of AZD2171 in Hepatocellular Carcinoma
This phase II trial is studying how well AZD2171 works in treating patients with locally advanced unresectable or metastatic liver cancer. AZD2171 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. Assess the progression free survival of patients with locally advanced unresectable or
metastatic hepatocellular carcinoma treated with AZD2171.
SECONDARY OBJECTIVES:
I. Determine the toxicity of this drug in these patients. II. Determine, preliminarily, the
efficacy of this drug, in terms of response rate, duration of response, and overall
survival, in these patients.
III. Determine the blood flow changes and vascular permeability of the tumor in patients
treated with this drug.
IV. Determine the pharmacokinetic profile of this drug in these patients.
OUTLINE: This is a multicenter study.
Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the
absence of disease progression or unacceptable toxicity. Dynamic contrast-enhanced (DCE) MRI
and CT perfusion scan of the liver are performed at baseline, 72 hours after the initial
dose of AZD2171, and at the end of course 1. Blood samples for pharmacokinetic studies are
collected periodically during study.
After the completion of study treatment, patients are followed every 3 months for 1 year.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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