NCT00621036

Vaccine Therapy and GM-CSF in Treating Patients With CNS Lymphoma

A Phase 2, Open-Label Study to Evaluate the Efficacy and Safety of Patient-Specific Immunotherapy, Recombinant Idiotype Conjugated to KLH (Id-KLH) and Administered With GM-CSF, in Patients With CNS Lymphoma

• Status: Withdrawn
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: University of Texas Southwestern Medical Center · Academic / Other
• Sex: All
• Age: 18 Years – 120 Years
• Healthy volunteers: Not accepted

Summary

RATIONALE: Vaccines made from a person's cancer proteins may help the body build an effective immune response to kill cancer cells. Colony-stimulating factors, such as GM-CSF, may increase the number of immune cells found in bone marrow or peripheral blood. Giving vaccine therapy together with GM-CSF may make a stronger immune response and kill more cancer cells. PURPOSE: This phase II trial is studying the side effects and how well giving vaccine therapy together with GM-CSF works in treating patients with CNS lymphoma.

Detailed description

OBJECTIVES: Primary * To determine the proportion of patients with CNS lymphoma who develop anti-idiotype (Id) and anti-keyhole limpet hemocyanin (KLH) humoral immune responses in the serum and/or CSF following patient-specific immunotherapy comprising recombinant tumor-derived immunoglobulin Id-KLH conjugate vaccine and sargramostim (GM-CSF). * To assess the safety and tolerability of this regimen in these patients. Secondary * To evaluate the progression-free survival (PFS) of patients treated with this regimen. * To determine the time to receipt of first subsequent anti-lymphoma therapy after initiating immunization with the Id-KLH conjugate vaccine. * To assess the correlation of anti-Id immune response in the CSF and/or serum with PFS and overall survival. Tertiary * To evaluate the kinetics of humoral immune response development in patients treated with this regimen. OUTLINE: * Pre-immunotherapy: Patients submit a tumor sample for manufacturing of the idiotype (Id)-keyhole limpet hemocyanin (KLH) conjugate vaccine and undergo placement of an Ommaya reservoir. Patients then receive induction therapy comprising methotrexate IV once every 2 weeks until a maximum radiographic response is achieved, as assessed by MRI of the brain. Patients then receive methotrexate IV once a month for 6 months. Patients with leptomeningeal or CSF involvement also receive intraventricular thiotepa twice a week until the CSF is clear on three evaluations and then once a week until the CSF is clear on four evaluations. Patients under 55 years of age also undergo whole brain radiotherapy (or craniospinal radiotherapy when extensive leptomeningeal disease is present). Patients who achieve a stable response to induction therapy proceed to immunotherapy. * Immunotherapy: Patients receive recombinant tumor-derived immunoglobulin Id-KLH conjugate vaccine subcutaneously (SC) on day 1 of weeks 0, 2, 4, 6, 8, 10, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, and 76. Patients also receive sargramostim (GM-CSF) SC on days 1-4 of the same weeks as the Id-KLH conjugate vaccine. After completion of therapy, patients are followed periodically for up to 2 years.

Conditions

• Brain and Central Nervous System Tumors
• Lymphoma
• Lymphoproliferative Disorder
• Small Intestine Cancer

Interventions

Type	Name	Description
BIOLOGICAL	autologous immunoglobulin idiotype-KLH conjugate vaccine
BIOLOGICAL	sargramostim
DRUG	methotrexate
DRUG	thiotepa
RADIATION	radiation therapy

Timeline

• Start date: 2007-10-19
• Primary completion: 2008-12-08
• Completion: 2008-12-08
• First posted: 2008-02-22
• Last updated: 2018-11-26

Locations

1 site across 1 country: United States