Clinical Trials Directory

Trials / Completed

CompletedNCT00029003

Gefitinib in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer

Phase II Trial of Chronic Oral ZD1839 (Iressa®) (NSC-715055) in Both Previously-Untreated and Previously-Treated Patients With Selected Stage IIIB and IV Bronchioloalveolar Carcinoma (BAC)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
90 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Phase II trial to study the effectiveness of gefitinib in treating patients who have stage IIIB or stage IV non-small cell lung cancer. Biological therapies such as gefitinib may interfere with the growth of the tumor cells and slow the growth of non-small cell lung cancer

Detailed description

PRIMARY OBJECTIVES: I. To assess the one-years survival rate in both previously-untreated and previously-treated patients with advanced bronchioalveolar carcinoma receiving chronic oral ZD1839. II. To assess the progression-free survival and overall survival in these groups of patients. III. To evaluate the frequency and severity of toxicities associated with this treatment regimen. IV. To evaluate the response rate using both the standard RECIST criteria and by computer-assisted image analysis in patients with measurable disease. V. To measure EGFR and EGFR variant III overexpression in tumor tissue samples and explore their relationship with aforementioned clinical outcomes. VI. To measure EGFR expression and activation status in slides of buccal brushings submitted on S9925 before and after initiation of treatment with ZD1839 and explore their association with response and survival. OUTLINE: This is a multicenter study. Patients are stratified according to prior systemic treatment for bronchioalveolar carcinoma (yes vs no). (The previously untreated stratum closed to accrual as of 2/15/2003.) Patients receive oral gefitinib once daily. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients are followed every 6 months for 2 years and then annually thereafter.

Conditions

Interventions

TypeNameDescription
DRUGgefitinibGiven orally
OTHERlaboratory biomarker analysisCorrelative studies

Timeline

Start date
2001-12-01
Primary completion
2004-12-01
First posted
2003-01-27
Last updated
2013-02-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00029003. Inclusion in this directory is not an endorsement.