Vaccine Therapy in Treating Patients With Malignant Glioma

Brain and Central Nervous System Tumors Clinical Trial

Official title:

Phase I Dose Escalation Study of Autologous Tumor Lysate-Pulsed Dendritic Cell Immunotherapy for Malignant Gliomas

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00068510
• Other study ID #: CDR0000327711
• Secondary ID: UCLA-0304053
• Status: Completed
• Phase: Phase 1
• Start date: June 2003
• Est. completion date: September 2012

Study information

• Verified date: August 2013
• Source: Jonsson Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Vaccines made from a person's white blood cells mixed with tumor proteins may make the body build an immune response to kill tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of vaccine therapy in treating patients with malignant glioma.

Description:

OBJECTIVES:

• Determine the dose-limiting toxicity and maximum tolerated dose of autologous tumor lysate-pulsed dendritic cells in patients with malignant gliomas.

• Determine survival, tumor progression, and cellular immune response in patients treated with this regimen.

OUTLINE: This is a dose-escalation study.

Patients undergo leukapheresis for the collection of peripheral blood mononuclear cells (PBMC). Autologous dendritic cells (DC) are prepared from autologous PBMC exposed to sargramostim (GM-CSF) and interleukin-4 and pulsed with autologous tumor lysate. Patients receive autologous tumor lysate-pulsed DC intradermally on days 0, 14, and 28 in the absence of unacceptable toxicity.

Cohorts of 6-12 patients receive escalating doses of autologous tumor lysate-pulsed DC until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Patients are followed every 2 months for 2 years.

PROJECTED ACCRUAL: A total of 3-18 patients will be accrued for this study within 9-18 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: September 2012
• Est. primary completion date: September 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Eligibility Criteria:

• Histologically confirmed diagnosis of one of the following malignant gliomas:

• Anaplastic astrocytoma

• Glioblastoma multiforme

• Anaplastic oligodendroglioma

• Malignant mixed oligoastrocytoma

• WHO grade III or IV disease

• Newly diagnosed disease

• Bidimensionally measurable disease by contrast-enhancing MRI

• Surgically accessible tumor for which resection is indicated

• Previously treated with or plan to undergo treatment with conventional external beam radiotherapy

• Age 18 and over

• Performance status Karnofsky 60-100%

• Life expectancy at least 8 weeks

• Hemoglobin at least 10 g/dL

• Absolute granulocyte count at least 1,500/mm^3

• Platelet count at least 100,000/mm^3

• SGOT and SGPT no greater than 2 times normal

• Alkaline phosphatase no greater than 2 times normal

• Bilirubin no greater than 1.5 mg/dL

• Hepatitis B negative

• Hepatitis C negative

• BUN no greater than 1.5 times normal

• Creatinine no greater than 1.5 times normal

• HIV negative

• Syphilis serology negative

• Afebrile

• Negative pregnancy test

• Fertile patients must use effective contraception

• At least 2 weeks since prior chemotherapy (6 weeks for nitrosoureas) and recovered.

• At least 2 weeks since prior corticosteroids

• At least 2 weeks since prior radiotherapy and recovered

• More than 72 hours since prior systemic antibiotics

Exclusion Criteria:

• active infection

• immunodeficiency

• autoimmune disease that may be exacerbated by immunotherapy, including any of the following:

• Rheumatoid arthritis

• Systemic lupus erythematosus

• Vasculitis

• Polymyositis-dermatomyositis

• Scleroderma

• Multiple sclerosis

• Juvenile-onset insulin-dependent diabetes

• allergy to study agents

• pregnant or nursing

• underlying condition that would contraindicate study therapy

• concurrent severe or unstable medical condition that would preclude giving informed consent

• psychiatric condition that would preclude study participation or giving informed consent

• other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, localized prostate cancer, or carcinoma in situ of the cervix

• concurrent chemotherapy during and for 2 weeks after administration of study vaccine

• concurrent corticosteroids prior organ allograft

• antihistamine therapy within 5 days before or after administration of study vaccine

• other concurrent investigational agents

• concurrent adjuvant therapy during and for 2 weeks after administration of study vaccine

Related Conditions & MeSH terms

• Brain and Central Nervous System Tumors
• Central Nervous System Neoplasms
• Glioma
• Nervous System Neoplasms

Intervention

Biological:
• therapeutic autologous dendritic cells

Locations

Country	Name	City	State
United States	Jonsson Comprehensive Cancer Center at UCLA	Los Angeles	California

Sponsors (2)

Lead Sponsor	Collaborator
Jonsson Comprehensive Cancer Center	National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Liau LM, Prins RM, Kiertscher SM, Odesa SK, Kremen TJ, Giovannone AJ, Lin JW, Chute DJ, Mischel PS, Cloughesy TF, Roth MD. Dendritic cell vaccination in glioblastoma patients induces systemic and intracranial T-cell responses modulated by the local centra — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose Limiting Toxicity		4 weeks
Secondary	Time to tumor progression, overall survival and cellular immune responses in brain tumor patients injected with tumor lysate pulsed dendritic cells		2 years