Vaccine Therapy in Treating Patients With Advanced Kidney Cancer

NCT ID: NCT00004880

Last Updated: 2020-08-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 1997-06-30

Brief Summary

RATIONALE: Vaccines may make the body build an immune response to kill tumor cells.

PURPOSE: Phase I trial to study the effectiveness of vaccine therapy in treating patients who have advanced kidney cancer.

Detailed Description

OBJECTIVES: I. Evaluate the safety of multiantigen loaded dendritic cells (DC) vaccine in patients with advanced renal cell carcinoma. II. Evaluate the immunologic response to this regimen in this patient population. III. Evaluate the clinical response to this regimen in this patient population.

OUTLINE: This is a sequential cohort study. All patients undergo total nephrectomy to harvest primary tumor for vaccine preparation. Patients without primary tumor undergo surgical resection of the accessible metastatic site for vaccine preparation. Patients are assigned to 1 of 4 treatment arms. Arm I: Patients receive vaccination with irradiated autologous tumor lysate (TuLy) intradermally (ID) on day 0 followed by vaccination with multiantigen liposome loaded dendritic cells (DC) ID on days 7, 14, and 21. Arm II: Patients receive vaccinations as in arm I, except DC are pulsed with tumor cells. Arm III: Patients receive vaccination with irradiated autologous tumor lysate (TuLy) IV on day 0 followed by vaccination with multiantigen liposome loaded DC IV on days 7, 14, and 21. Arm IV: Patients receive vaccinations as in arm III, except DC are treated as in arm II. Patients are followed on days 28, 42, 70, and 112.

PROJECTED ACCRUAL: A total of 24 patients will be accrued for this study.

Conditions

Kidney Cancer

Study Design

• Primary Study Purpose: TREATMENT

Interventions

dendritic cell vaccine therapy

Intervention Type: BIOLOGICAL

conventional surgery

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed metastatic renal cell carcinoma Evaluable or bidimensionally measurable disease with primary renal tumor in place or surgically accessible metastatic site greater than 2 x 2 cm
• Over 18
• ECOG 0-1
• Hematopoietic:

• Hemoglobin at least 10 g/dL (not transfusion dependent)
• Platelet count at least 75,000/mm3
• WBC greater than 3,000/mm3
• Hepatic: SGOT/SGPT no greater than 5 times upper limit of normal (ULN)
• Alkaline phosphatase no greater than 5 times ULN
• PT/PTT no greater than 1.5 times ULN
• Bilirubin no greater than 2.5 mg/dL
• Renal: Creatinine no greater than 2.0 g/dL
• Hepatitis B surface antigen negative
• Negative pregnancy test
• Fertile patients must use effective contraception
• At least 4 weeks since prior immunotherapy
• At least 4 weeks since prior chemotherapy
• At least 4 weeks since prior radiotherapy
• At least 14 days since prior acute therapy for infection

Exclusion Criteria

• uncontrolled CNS metastasis
• ischemic heart disease that precludes surgery
• pulmonary condition that precludes surgery
• other underlying condition or allergy that would preclude study
• acute viral, bacterial, or fungal infection requiring therapy HIV negative
• pregnant or nursing
• other acute medical problems that would preclude study
• concurrent corticosteroids (oral, topical, inhaled)
• prior organ allografts

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Jonsson Comprehensive Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Barbara J. Gitlitz, MD

Role: STUDY_CHAIR

Jonsson Comprehensive Cancer Center

Locations

Jonsson Comprehensive Cancer Center, UCLA

Los Angeles, California, United States

Countries

United States

Other Identifiers

UCLA-9703025

Identifier Type: -

Identifier Source: secondary_id

NCI-G00-1675

Identifier Type: -

Identifier Source: secondary_id

CDR0000067542

Identifier Type: -

Identifier Source: org_study_id