Vaccine Therapy in Treating Patients With Stage IV Melanoma
NCT ID: NCT00042783
Last Updated: 2013-06-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
INTERVENTIONAL
2002-09-30
2006-03-31
Brief Summary
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PURPOSE: Phase II trial to study the effectiveness of vaccine therapy in treating patients who have stage IV melanoma.
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Detailed Description
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* Determine the feasibility of treating patients with stage IV melanoma with D1/3-MAGE-3-His fusion protein with SB-AS02B adjuvant.
* Determine the clinically confirmed response rates (partial and complete responses) of patients treated with this regimen.
* Determine the 6-month progression-free survival rate of patients treated with this regimen.
* Determine the qualitative and quantitative toxic effects of this regimen in these patients.
* Determine immune responses in patients treated with this regimen.
OUTLINE: This is a multicenter study.
Patients receive D1/3-MAGE-3-His fusion protein emulsified in SB-AS02B adjuvant intramuscularly once every 3 weeks for a total of 12 weeks (4 injections). In the absence of disease progression or unacceptable toxicity, patients receive a second 12-week course beginning at week 16.
Patients are followed every 3 months for 1 year and then every 6 months for 2 years.
PROJECTED ACCRUAL: A total of 25-45 patients will be accrued for this study within 5-9 months.
Conditions
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Study Design
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TREATMENT
NONE
Interventions
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D1/3-MAGE-3-His fusion protein
SB-AS02B adjuvant
Eligibility Criteria
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Inclusion Criteria
* Histologically confirmed stage IV melanoma that is considered incurable by surgery, radiotherapy, or limb perfusion
* M1a or M1b disease
* Measurable disease outside prior field of limb perfusion
* Metastatic mucosal melanoma allowed
* MAGE-3 positive by reverse transcription polymerase chain reaction
* No uveal or choroidal primary melanoma
* No prior or concurrent brain metastases by CT scan or MRI of the brain
PATIENT CHARACTERISTICS:
Age
* Not specified
Performance status
* Zubrod 0-1
Life expectancy
* Not specified
Hematopoietic
* Not specified
Hepatic
* Hepatitis B surface antigen negative
* Hepatitis C negative
* No liver cirrhosis
* No unstable liver disease
* No coagulation disorders
Renal
* Not specified
Cardiovascular
* No major cardiovascular illness
* No myocardial infarction within the past 6 months
Pulmonary
* No major pulmonary illness
Other
* Not pregnant or nursing
* Fertile patients must use effective contraception
* HIV negative
* No AIDS or HIV-1-associated complex
* No chronic alcohol abuse or drug addiction
* No systemic infections
* No prior active autoimmune disease
* No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or adequately treated stage I or II cancer from which the patient is currently disease-free
PRIOR CONCURRENT THERAPY:
Biologic therapy
* At least 4 weeks since prior adjuvant biologic therapy
* No prior biologic therapy for stage IV melanoma
* No prior MAGE-3 peptide or protein vaccine preparation
Chemotherapy
* At least 4 weeks since prior adjuvant chemotherapy
* No prior chemotherapy for stage IV melanoma
Endocrine therapy
* Not specified
Radiotherapy
* At least 4 weeks since prior adjuvant radiotherapy
Surgery
* At least 4 weeks since prior surgery
Other
* See Disease Characteristics
* At least 3 weeks since prior limb perfusion and recovered
* At least 4 weeks since other prior adjuvant therapy
* No other prior therapy for stage IV melanoma
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
SWOG Cancer Research Network
NETWORK
Principal Investigators
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Jeffrey S. Weber, MD, PhD
Role: STUDY_CHAIR
University of Southern California
Locations
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Arizona Cancer Center at University of Arizona Health Sciences Center
Tucson, Arizona, United States
USC/Norris Comprehensive Cancer Center and Hospital
Los Angeles, California, United States
Jonsson Comprehensive Cancer Center, UCLA
Los Angeles, California, United States
Barbara Ann Karmanos Cancer Institute
Detroit, Michigan, United States
Veterans Affairs Medical Center - Biloxi
Biloxi, Mississippi, United States
CCOP - Columbia River Oncology Program
Portland, Oregon, United States
University of Washington School of Medicine
Seattle, Washington, United States
Countries
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Other Identifiers
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SWOG-S0116
Identifier Type: -
Identifier Source: secondary_id
CDR0000069468
Identifier Type: -
Identifier Source: org_study_id
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