RATIONALE: Vaccines made from a tumor antigen may help the body build an effective immune response to kill tumor cells. PURPOSE: This phase I/II trial is studying the side effects and how well vaccine therapy works in treating patients who have received first-line therapy for Hodgkin's lymphoma.
OBJECTIVES: * Determine immunologic responses in patients who have completed first-line therapy for Hodgkin's lymphoma treated with Hodgkin's antigens-GM-CSF-expressing cell vaccine. * Determine the durability of these immunologic responses in these patients. * Determine the utility of an Epstein-Barr virus reporter system for monitoring cellular vaccine responses. * Determine the safety and tolerability of this vaccine in these patients. OUTLINE: Beginning 4-6 months after last chemotherapy, patients receive Hodgkin's antigens-GM-CSF-expressing cell vaccine on day 1. Treatment repeats every 3 weeks for up to 4 courses. Immunologic responses are serially monitored along with disease status. PROJECTED ACCRUAL: A total of 35 patients will be accrued for this study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
1
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Baltimore, Maryland, United States
Immunologic Response
Time frame: 9 months
Durability of Immunologic Response
Time frame: 2 years
Utility of Epstein-Barr Virus Reporter System for Monitoring Cellular Vaccine Responses
Time frame: 2 years
Safety and Tolerability
Time frame: After administration of last vaccine at 9 weeks
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