Clinical Trials Directory

Trials / Terminated

TerminatedNCT00074295

S0310: Vaccine Therapy in Treating Patients With Stage IIIB or Stage IV Bronchoalveolar Lung Cancer

Phase II Trial of CG8123, an Autologous Cancer Vaccine (GVAX), in Patients With Selected Stage IIIB and IV Bronchioloalveolar Carcinoma (BAC)

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
19 (actual)
Sponsor
SWOG Cancer Research Network · Network
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Vaccines made from a person's tumor tissue may make the body build an immune response to kill tumor cells. PURPOSE: This phase II trial is studying vaccine therapy to see how well it works in treating patients with stage IIIB or stage IV bronchoalveolar (lung) cancer.

Detailed description

OBJECTIVES: * Determine the progression-free and overall survival of patients with selected stage IIIB or stage IV bronchoalveolar carcinoma treated with GVAX lung cancer vaccine. * Determine the response rate (confirmed and unconfirmed and complete and partial) in patients treated with this vaccine. * Determine the frequency and severity of toxic effects of this vaccine in these patients. * Determine the functional status of patients treated with this vaccine. * Correlate systemic biologic activity (i.e., antigen-specific antitumor and systemic cytokine responses) with clinical outcome in patients treated with this vaccine. OUTLINE: This is a multicenter study. Patients are stratified according to prior systemic cancer therapy for bronchoalveolar carcinoma (BAC) (yes vs no) and pattern of BAC (diffuse vs nodular). After successful vaccine manufacturing from tumor tissue procured, patients receive GVAX lung cancer vaccine intradermally (ID) (6-7 injections per vaccination) on weeks 1, 3, 5, 7, and 9 for a total of 5 vaccinations. Treatment continues in the absence of disease progression or unacceptable toxicity. Quality of life is assessed at baseline and at weeks 9, 13, and 21. Patients are followed at 4 weeks, every 8 weeks for 1 year, and then every 12 weeks for 2 years. PROJECTED ACCRUAL: A total of 117 patients (67 previously untreated and 50 previously treated) will be accrued for this study.

Conditions

Interventions

TypeNameDescription
BIOLOGICALGVAX lung cancer vaccine6-7 injections per week in rotating locations for five weeks

Timeline

Start date
2004-03-01
Primary completion
2007-08-01
Completion
2007-08-01
First posted
2003-12-11
Last updated
2012-07-24

Source: ClinicalTrials.gov record NCT00074295. Inclusion in this directory is not an endorsement.