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

Phase 2
Terminated
Conditions
Lung Cancer
Interventions
Biological: GVAX lung cancer vaccine
Registration Number
NCT00074295
Lead Sponsor
SWOG Cancer Research Network
Brief 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.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
19
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
treatmentGVAX lung cancer vaccineGVAX lung cancer vaccine
Primary Outcome Measures
NameTimeMethod
Functional status
Toxicity
Progression-free and overall survival
Correlation of systemic biologic activity with clinical outcome
Response rate
Secondary Outcome Measures
NameTimeMethod
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