Vaccine Therapy in Treating Patients With Metastatic Melanoma

University of Virginia22 enrolled

Overview

RATIONALE: Vaccines made from peptide 946 may make the body build an immune response to kill tumor cells. Combining these vaccines with proteins from the tetanus vaccine, and/or with either QS21 or Montanide ISA-51 may be an effective treatment for metastatic melanoma. PURPOSE: Randomized phase I trial to study the effectiveness of vaccines made from peptide 946 with or without tetanus peptide, QS21, or Montanide ISA-51 in treating patients with metastatic melanoma that cannot be surgically removed or with melanoma that is likely to recur.

OBJECTIVES: I. Determine the safety of peptide 946 melanoma vaccine (peptide 946), peptide 946 combined with tetanus peptide melanoma vaccine, or peptide 946-tetanus peptide conjugate in patients with high risk melanoma. II. Determine the immunogenicity of peptide 946 melanoma vaccine (peptide 946), peptide 946 combined with tetanus peptide melanoma vaccine, or peptide 946-tetanus peptide conjugate in patients with high risk melanoma. OUTLINE: This is a randomized, open-label study. Patients are randomized to 1 of 6 treatment arms: Arm I: Patients receive peptide 946 melanoma vaccine (peptide 946) emulsified with QS21 subcutaneously (SQ). Arm II: Patients receive peptide 946 emulsified with Montanide ISA-51 (ISA-51) SQ. Arm III: Patients receive peptide 946 combined with tetanus peptide melanoma vaccine (tetanus peptide) emulsified with QS21 SQ. Arm IV: Patients receive peptide 946 combined with tetanus peptide emulsified with ISA-51 SQ. Arm V: Patients receive peptide 946-tetanus peptide conjugate emulsified with QS21 SQ. Arm VI: Patients receive peptide 946-tetanus peptide conjugate emulsified with ISA-51 SQ. Initially, 4 patients are randomized to Arm I and 4 patients are randomized to Arm II. If no dose limiting toxicities are observed in these patients, then additional patients are randomized to arms III-VI. Patients in each arm receive vaccine on day 0 and at months 1, 2, 3, 6, 9, and 12. Patients are followed at 6 and 12 months. PROJECTED ACCRUAL: A maximum of 36 patients will be accrued for this study.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Melanoma (Skin)

Interventions

QS21BIOLOGICAL

vaccine adjuvant

IFA (incomplete Freund's adjuvant)BIOLOGICAL

Peptides emulsified in IFA.

p946BIOLOGICAL

This a nonamer peptide YLEPGPVTA from Gp100, used as a melanoma vaccine antigen.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 79 Years

Medical Language ↔ Plain English

Inclusion criteria: * Histologically confirmed unresectable metastatic melanoma (AJCC stage III or IV) OR resected melanoma with high risk of recurrence or mortality (stage IIB and above) * Age: 18 to 79 * Performance status: ECOG 0-2 * Life expectancy: Greater than 12 months * Hematopoietic: Absolute neutrophil count greater than 1,000/mm3 Platelet count greater than 100,000/mm3 Hemoglobin greater than 9 g/dL * Hepatic: AST and ALT no greater than 2.5 times upper limit of normal (ULN) Bilirubin no greater than 2.5 times ULN Alkaline phosphatase no greater than 2.5 times ULN * Renal: Creatinine no greater than 1.5 times ULN Exclusion criteria: * patients currently receiving cytotoxic chemotherapy or who have received that therapy within the preceding 3 months * known or suspected allergies to any component of the treatment vaccine * unresectable tumor llikely to cause symptoms and for which therapy is anticipated within 3 months. * receiving acute treatment for seriouis infection within 14 days. * Patients with bulky disease, or with multiple brain metastases, but solitary brain metastases treated successfully with surgery or gamma knife may be eligible. * Any of the following with 3 months: * agentes with putative immunomodulating activity (except NSAIDs) * allergy desensitizing injections * other investigational agents * interferons * corticosteroids * any growth factors * prior melanoma vaccinations * pregnancy or the possibility of becoming pregnant on study * medical contraindication or potential problems in complying with the requirements of the protocol.

Locations (1)

Cancer Center, University of Virginia HSC

Charlottesville, Virginia, United States

Outcomes

Primary Outcomes

Safety: Grade 3 Adverse Events

Adverse events are monitored according to NCI/DCT Common Toxicity Criteria

Time frame: Up to 24 months after last vaccine

Secondary Outcomes

Immunogenicity of Each Vaccine Regimen

T cell responses to the p946 (gp100 \[280-288\]) peptide. All enrolled patients were assayed for immune response to the gp100 peptide by ELIspot assay after 14 days in vitro sensitization. The number with a response in each study arm is reported.

Time frame: up to 12 months since enrollment

Data from ClinicalTrials.gov

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