Lymphoma, Low-Grade
Conditions
Keywords
lymphoma, vaccine, idiotype, KLH, GM-CSF
Brief summary
The purpose of this study was to determine if an idiotype vaccine, made from a patient's lymphoma that has returned after chemotherapy and/or rituximab, would be able to shrink their tumor.
Detailed description
The purpose of this study was to assess the ability of active immunotherapy to induce tumor regressions in relapsed low-grade lymphoma. B-cell malignancies express a unique antigen, the immunoglobulin idiotype (Id), on their surface. Each B-cell harbors a unique genetic sequence used in the production of immunoglobulin idiotype. B-cell lymphomas arise from the clonal expansion of a single B-cell and all tumor cells express that unique Id protein. No normal B-cells possess that Id on their cell surface. Hence, Id protein should serve as an ideal target for individualized active immune therapy of NHL. Many of the antigens expressed by tumors (including Id) are only weak immunogens. To augment the immune response against Id, the Id protein must be chemically coupled to a strongly immunogenic protein. Keyhole limpet hemocyanin (KLH) is a commonly used protein carrier capable of augmenting the body's immune reaction against Id protein. While initial studies reported a predominately humoral (antibody) response, cellular immunity (T-cells) also plays a critical role in anti-tumor immunity. GM-CSF is a hematopoietic growth factor that stimulates T-cell proliferation.
Interventions
BIOLOGICALFavId (Id-KLH) active immunotherapy
Sponsors
Favrille
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 18 years of age * Histologically confirmed grade 1 or 2 follicular B-cell lymphoma (WHO classification) * Patients that have responded with at least stable disease to their most recent chemo- or anti-CD20 antibody (Rituxan®, Zevalin, Bexxar) therapy for a minimum of 90 days and who currently have relapsed or who continue to have stable disease. * Tumor accessible for biopsy or previously existing biopsy material * At least 1 additional bidimensional lesion measuring at least 2 cm in each dimension * Performance status (ECOG) of 0, 1 or 2 * Absolute Granulocyte count ? 1,000/mm3 * Total Bilirubin \< 2 mg/dL * AST and ALT \< 2x Upper Limit of Normal * Creatinine \< 1.5 mg/dL
Exclusion criteria
* Patients who have had more than 3 prior chemotherapy or anti-CD20 regimens * Prior fludarabine * Prior tumor-specific idiotype immunotherapy * Patients whose disease has progressed within the first 90 days of their last chemotherapy or anti-CD20 treatment * Concurrent immunosuppressive therapy (high-dose steroids; etc) * Prior splenectomy * Surgery, cancer radiotherapy, steroid therapy, immunotherapy or chemotherapy within 90 days prior to first scheduled vaccination * Known history of CNS lymphoma or meningeal lymphomatosis * HIV positive * Serious non-malignant disease (e.g., psychiatric disorders, congestive heart failure, or active uncontrolled bacterial, viral, or fungal infections), or other conditions which, in the opinion of the investigator would compromise protocol objectives * Prior malignancy (excluding nonmelanoma carcinomas of the skin and in situ cervical carcinomas) unless in remission for \> 2 years * Treatment with an investigational drug within 30 days prior to study entry * Pregnant or nursing women NOTE: Women of childbearing potential should be advised to avoid becoming pregnant while receiving treatment with FavId.
Countries
United States
Outcome results
None listed