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Vaccine Therapy With or Without Interleukin-2 in Treating Patients With Metastatic Melanoma

Primary Purpose

Melanoma (Skin)

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
aldesleukin
fowlpox virus vaccine vector
gp100 antigen
Sponsored by
National Cancer Institute (NCI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Melanoma (Skin) focused on measuring stage IV melanoma, recurrent melanoma

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Histologically proven metastatic melanoma that has failed standard treatment Measurable disease HLA-A-201 positive PATIENT CHARACTERISTICS: Age: 16 and over Performance status: ECOG 0-2 Life expectancy: More than 3 months Hematopoietic: WBC ≥ 3,000/mm^3 Platelet count ≥ 90,000/mm^3 No coagulation disorders Hepatic: Bilirubin ≤ 1.6 mg/dL (less than 3.0 mg/dL for patients with Gilbert's syndrome) AST/ALT < 2 times normal Hepatitis B surface antigen negative Renal: Creatinine ≤ 2.0 mg/dL Cardiovascular: No major cardiovascular disease No cardiac ischemia by a stress thallium test or other comparable test* No myocardial infarction* No cardiac arrhythmias* NOTE: *In order to be eligible to receive interleukin-2 (IL-2) Pulmonary: No major respiratory disease No obstructive or restrictive pulmonary disease* NOTE: *In order to be eligible to receive IL-2 Immunologic: No autoimmune disease No known immunodeficiency disease No primary or secondary immunodeficiency No allergy to eggs No active systemic infections HIV negative Other: Not pregnant Negative pregnancy test Fertile patients must use effective contraception No other active major medical illness* NOTE: *In order to be eligible to receive IL-2 PRIOR CONCURRENT THERAPY: Biologic therapy: No prior gp100 vaccination Chemotherapy: Not specified Endocrine therapy: No concurrent steroids Radiotherapy: Not specified Surgery: Prior surgery for the malignancy allowed Other: At least 3 weeks since other prior therapy for the malignancy

Sites / Locations

  • Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
July 11, 2001
Last Updated
June 19, 2013
Sponsor
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00019669
Brief Title
Vaccine Therapy With or Without Interleukin-2 in Treating Patients With Metastatic Melanoma
Official Title
Immunization of Patients With Metastatic Melanoma Using a Recombinant Fowlpox Virus Encoding a GP100 Peptide Preceded by an Endoplasmic Reticulum Insertion Signal Sequence
Study Type
Interventional

2. Study Status

Record Verification Date
August 2004
Overall Recruitment Status
Completed
Study Start Date
October 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Cancer Institute (NCI)

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Vaccines may make the body build an immune response to kill tumor cells. It is not yet known whether combining melanoma vaccine with interleukin-2 is more effective than vaccine therapy alone in treating metastatic melanoma. PURPOSE: Phase II trial to compare the effectiveness of melanoma vaccine and interleukin-2 with that of melanoma vaccine alone in treating patients who have metastatic melanoma that has not responded to previous treatment.
Detailed Description
OBJECTIVES: Compare the clinical response in patients with metastatic melanoma treated with immunization with recombinant fowlpox vaccine administered either intravenously or intramuscularly, with or without interleukin-2 (IL-2). Compare the immune response in patients before and after treatment with these regimens. Compare the toxicity profile of these regimens in these patients. OUTLINE: This is a partially randomized study. Patients are randomized to 1 of 3 treatment cohorts. Cohort 1: Patients receive recombinant fowlpox virus encoding gp100 peptide (fowlpox vaccine) IV once every 4 weeks for up to 4 doses. (Closed to accrual as of 6/21/02.) Cohort 2: Patients receive fowlpox vaccine intramuscularly (IM) once every 4 weeks for up to 4 doses. (Closed to accrual as of 6/21/04.) Cohort 3 (for patients in need of immediate interleukin-2 [IL-2] and those with disease progression after treatment in cohorts 1 or 2): Patients receive fowlpox vaccine either IV or IM* once every 4 weeks for 4 doses and IL-2 IV every 8 hours for a maximum of 12 doses beginning 24 hours after fowlpox vaccine. NOTE: *The IM route of administration was selected as the preferred route of administration from cohorts 1 and 2 Expanded cohort 2 (open to accrual 7/19/02): Patients receive fowlpox vaccine IM once every 4 weeks for up to 4 doses. Upon disease progression, patients receive fowlpox vaccine as above and IL-2 IV every 8 hours for a maximum of 12 doses beginning 24 hours after fowlpox vaccine. (Closed to accrual 12/4/03.) In all cohorts, 3-4 weeks after the last injection, patients achieving a complete remission may receive a maximum of an additional 2 courses of therapy. Patients with responding disease may receive repeat vaccinations for up to 8 courses. Patients with no response or progressive disease in cohorts not receiving IL-2 may be treated with fowlpox vaccine and IL-2 as in cohort 3. Patients who are randomized to receive IL-2 may not receive additional IL-2 therapy. PROJECTED ACCRUAL: A maximum of 84 patients (24 in cohorts 1 and 2, 19-33 in cohort 3, and 27 in expanded cohort 2) will be accrued for this study within 1 year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma (Skin)
Keywords
stage IV melanoma, recurrent melanoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Masking
None (Open Label)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
aldesleukin
Intervention Type
Biological
Intervention Name(s)
fowlpox virus vaccine vector
Intervention Type
Biological
Intervention Name(s)
gp100 antigen

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically proven metastatic melanoma that has failed standard treatment Measurable disease HLA-A-201 positive PATIENT CHARACTERISTICS: Age: 16 and over Performance status: ECOG 0-2 Life expectancy: More than 3 months Hematopoietic: WBC ≥ 3,000/mm^3 Platelet count ≥ 90,000/mm^3 No coagulation disorders Hepatic: Bilirubin ≤ 1.6 mg/dL (less than 3.0 mg/dL for patients with Gilbert's syndrome) AST/ALT < 2 times normal Hepatitis B surface antigen negative Renal: Creatinine ≤ 2.0 mg/dL Cardiovascular: No major cardiovascular disease No cardiac ischemia by a stress thallium test or other comparable test* No myocardial infarction* No cardiac arrhythmias* NOTE: *In order to be eligible to receive interleukin-2 (IL-2) Pulmonary: No major respiratory disease No obstructive or restrictive pulmonary disease* NOTE: *In order to be eligible to receive IL-2 Immunologic: No autoimmune disease No known immunodeficiency disease No primary or secondary immunodeficiency No allergy to eggs No active systemic infections HIV negative Other: Not pregnant Negative pregnancy test Fertile patients must use effective contraception No other active major medical illness* NOTE: *In order to be eligible to receive IL-2 PRIOR CONCURRENT THERAPY: Biologic therapy: No prior gp100 vaccination Chemotherapy: Not specified Endocrine therapy: No concurrent steroids Radiotherapy: Not specified Surgery: Prior surgery for the malignancy allowed Other: At least 3 weeks since other prior therapy for the malignancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven A. Rosenberg, MD, PhD
Organizational Affiliation
NCI - Surgery Branch
Official's Role
Study Chair
Facility Information:
Facility Name
Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892-1182
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
12912944
Citation
Rosenberg SA, Yang JC, Schwartzentruber DJ, Hwu P, Topalian SL, Sherry RM, Restifo NP, Wunderlich JR, Seipp CA, Rogers-Freezer L, Morton KE, Mavroukakis SA, Gritz L, Panicali DL, White DE. Recombinant fowlpox viruses encoding the anchor-modified gp100 melanoma antigen can generate antitumor immune responses in patients with metastatic melanoma. Clin Cancer Res. 2003 Aug 1;9(8):2973-80.
Results Reference
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Vaccine Therapy With or Without Interleukin-2 in Treating Patients With Metastatic Melanoma

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