The Role of Peptide-loaded Dendritic Cells to Augment the Therapeutic Effect of Interleukin-2

Hadassah Medical Center

Status and phase

Completed

Phase 2

Phase 1

Conditions

Metastatic Melanoma

Treatments

Procedure: Immunotherapy treatment for melanoma

Study type

Interventional

Funder types

Other

Identifiers

NCT00279058

pepDCIL2- HMO-CTIL

Details and patient eligibility

About

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.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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.
serum creatinine of 2.0 mg/dl or less,
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.
WBC 3000/mm3 or greater
platelet count 90,000 mm3 or greater
serum AST/ALT less then two times normal
ECOG performance status of 0, 1 or 2.
Patients of both genders must be willing to practice effective birth control during this trial.
Patient agreed to participate in the study and has signed a written informed consent,
The patient must be eligible to receive IL-2.

Exclusion criteria

Patients will be excluded:

who are undergoing or have undergone in the past 3 weeks any other form of therapy except from surgery for their cancer.
have active systemic infections, coagulation disorders, autoimmune disease or other major medical illnesses of the cardiovascular or respiratory systems or any known immunodeficiency disease.
who require steroid therapy.
who are pregnant (because of possible side effects on the fetus).
who are known to be positive for hepatitis BsAG, HCV, or HIV antibody (because of possible immune effects of these conditions).
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.)
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).