Non-small Cell Lung Cancer Clinical Trial
Official title:
Pazopanib and Weekly Paclitaxel in Stage IIIB/IV Non-small Cell Lung Cancer
Lung cancer is the leading cause of cancer worldwide with approximately 1.2 million new cases each year. Non-small cell lung cancer (NSCLC) accounts for greater than 80% of all lung carcinomas in Western countries. Surgical resection is the treatment of choice for patients with early stage disease (Stage I and II), but at least 50% of these patients will relapse locally and/or develop distant metastases. Furthermore, 70% of patients with NSCLC are non-resectable at the time of their diagnosis due to either locally advanced or metastatic disease. The long-term prognosis for patients with NSCLC remains poor with the overall 5-year survival rate less than 15%. The low survival rate may be attributed to the high incidence of unresectable disease at presentation and the inability of systemic therapy to cure metastatic disease. There is a clear need for improvement in the treatment of NSCLC.
The primary objective of this study is to evaluate the objective response rate of pazopanib
in combination with paclitaxel in the treatment of subjects with advanced NSCLC. Tumor
response will be assessed according to the Response Evaluation Criteria in Solid Tumors
(RECIST) criteria (version 1.1). A subject is defined as a responder if he/she sustains a
complete response (CR) or a partial response (PR) for at least 4 weeks at any time during
treatment. A subject without a post-baseline assessment of response will be considered a
non-responder.
A secondary objective of this study is to evaluate the safety and tolerability of pazopanib
in combination with paclitaxel in the treatment of subjects with advanced NSCLC. Safety and
tolerability endpoints will consist of the evaluation of adverse events (AEs), exposure,
withdrawals due to AEs, dose reductions or interruptions, and changes from baseline in vital
signs and clinical laboratory parameters.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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