Metastatic Melanoma
Conditions
Brief summary
Melanoma is the main cause of death in patients with skin cancer. Once it has metastasized, this cancer has been shown to respond to chemotherapy only in rare cases. Immunotherapy represents an approach to treatment based on the immune response to cancer antigens. The principal objective of the study is to identify whether a dendritic cell-based vaccine can increase the moderate therapeutic effect of bolus high dose IL-2 in patients with metastatic melanoma. For this purpose,patients with metastatic melanoma who have a certain blood type (HLA-A201+) will be treated systemically with high dose IL-2. In one group of patients, the IL-2 will be preceded by three doses of autologous dendritic cell pulsed with melanoma antigens appropriate for their blood type. Two cycles of three DC vaccines will be administered every 14 days by intra-lymph node injections, followed by high dose IL-2 treatment. Responding patients will receive additional DC vaccines at 1 month and 2 months intervals. In a second group, patients will receive the standard high dose IL-2 protocol within a comparable period of time. Each group will include 12 patients. A complete evaluation of evaluable lesions will be performed prior to accrual, after initial 3 DC vaccines, six weeks after first IL-2 treatment, after a total of 6 DC vaccines and 6 weeks after second cycle of IL-2 treatment.
Interventions
PROCEDUREImmunotherapy treatment for melanoma
Sponsors
Hadassah Medical Organization
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Any patient age 18 to 65, with measurable metastatic melanoma who has an expected survival of greater than three months. All patients will be HLA-A2 positive * Patient must have received accepted standard treatmnet for melanoma - DTIC -containing protocol ,unless unwilling. * Patients who failed previous treatment with IL-2 will be included on a compassionate basis in the IL-2 plus vaccination scheme without being included in the analysis. 2. serum creatinine of 2.0 mg/dl or less, 3. Total bilirubin 1.6 mg/dl or less, except for patients with Gilbert's Syndrome who must have a total bilirubin less than 3.0 mg/dl. 4. WBC 3000/mm3 or greater 5. platelet count 90,000 mm3 or greater 6. serum AST/ALT less then two times normal 7. ECOG performance status of 0, 1 or 2. 8. Patients of both genders must be willing to practice effective birth control during this trial. 9. Patient agreed to participate in the study and has signed a written informed consent, 10. The patient must be eligible to receive IL-2.
Exclusion criteria
Patients will be excluded: 1. who are undergoing or have undergone in the past 3 weeks any other form of therapy except from surgery for their cancer. 2. have active systemic infections, coagulation disorders, autoimmune disease or other major medical illnesses of the cardiovascular or respiratory systems or any known immunodeficiency disease. 3. who require steroid therapy. 4. who are pregnant (because of possible side effects on the fetus). 5. who are known to be positive for hepatitis BsAG, HCV, or HIV antibody (because of possible immune effects of these conditions). 6. who have any form of primary or secondary immunodeficiency. (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who have decreased immune competence may be less responsive to the experimental treatment and more susceptible to its toxicities.) 7. who are allergic to eggs. i. who have an active major medical illnesses such as cardiac ischemia as evidenced by a stress thallium or comparable test, myocardial infarction, cardiac arrhythmias, obstructive or restrictive pulmonary disease (to be eligible to receive IL-2 ) j. Have an abnormal thyroid function (to be eligible to receive IL-2).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complete evaluation of untreated lesions with physical examination and appropriate X-rays and/or scans will be performed four to six weeks after the last DC injection. | — |
| Immunological evaluation will be performed two weeks after the last DC injection. | — |
Countries
Israel
Outcome results
None listed