High-Risk Melanoma Clinical Trial
Official title:
Evaluation of the Impact of Adjuvants Accompanying Peptide Immunization in High Risk Melanoma
This study will evaluate the immunization effects of a vaccine for patients who are at risk
for recurrence of their skin cancer. That is, the risk of cancer is higher if melanoma has
invaded deep into the skin or lymph nodes. Currently, the only therapy that the U.S. Food
and Drug Administration (FDA) has approved for preventing recurrence of melanoma is
alpha-interferon. But the research data are controversial. In this study, the vaccine to be
used, called gp100, contains a piece of a protein called a peptide, which melanoma cancer
cells produce.
Patients 16 and older who have had confirmed melanoma surgically removed and whose tissue
type is tested as being human leukocyte antigen serotype within HLA-A serotype group
(HLA-A2), through a specific blood test, may be eligible for this study.
Up to 132 participants will be enrolled. There will be a physical examination and collection
of blood samples for tests, and making sure that x-rays and scans are current. Patients will
be randomly assigned to four groups. Group 1 will receive the peptide with an adjuvant
(assistant) oil-based liquid called Montanide ISA-51, as an injection in the thigh. Group 2
will receive gp100, Montanide, and a cream called imiquimod, which the FDA has approved for
treating genital warts and herpes but that may help immune cells in the skin to recognize
the vaccine. Imiquimod will be applied to the skin for 5 days. Group 3 will receive gp100
mixed in salt water given as several mini-doses under the skin of the thigh. Group 4 will
also receive several mini-doses of gp100 mixed in saline, as well as imiquimod cream applied
to the skin for 5 days. All patients will receive the gp100 every 3 weeks for 12 weeks.
Every dose is a cycle, with four cycles considered a course of therapy. If the melanoma does
not return or patients do not experience side effects from this therapy, then the courses of
vaccine will repeated for up to 12 cycles of therapy (3 courses over 33 weeks). Side effects
of the peptide vaccination include local swelling, swelling of local lymph nodes, bruising,
and pain and redness at the injection sites. There may be chills or fever. Patients will be
watched closely for such side effects.
To study how the vaccine changes the action of cells in the immune system, patients' white
blood cells (lymphocytes) will be obtained, involving a separate informed consent. The
procedure, called leukaphersis, requires inserting a needle into the arm, to obtain blood
going into a machine, which divides the blood into red cells, plasma (or the serum part),
and lymphocytes. The lymphocytes are removed, and the plasma and red cells returned to the
patient through a second needle in the other arm. Risks associated with the procedure
include fainting, which can be prevented by patients' eating before coming to the lab, and
bleeding and infection at the needle site. Patients will undergo leukapheresis will be done
about four times: before receiving the vaccine, 3 weeks after the first four doses, and then
after 8 cycles and 12 cycles. Patients assigned to the groups receiving imiquimod will be
asked to record every time they apply that cream and describe any symptoms developed during
the study. All patients will be watched closely for any sign that their melanoma has
returned. Before and throughout the study, multiple blood tests will be conducted.
The vaccine, Montanide, and imiquimod may increase patients' immune system in fighting off
new tumors, but that is not known now. However, the study may provide information that will
be useful in treating melanoma patients in the future.
| Status | Completed |
| Enrollment | 104 |
| Est. completion date | May 2010 |
| Est. primary completion date | May 2010 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 7 Years and older |
| Eligibility |
- INCLUSION CRITERIA: HLA-A 0201 patients, age greater than or equal to 16 years, primary melanomas with lesions that are ulcerated and greater than or equal to 2mm, or any lesions that are greater than or equal to 4.0 mm in thickness, or greater than or equal to1 positive lymph node, or local recurrence, or resected metastatic disease, within 6 months of surgical resection will be considered. Patients must be clinically disease free at the time of protocol entry as documented by radiologic studies within 6 weeks of patient entry. 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/mm^3 or greater, Platelet count 90,000 mm^3 or greater, Serum aspartate aminotransferase (AST)/alanine aminotransferase (ALT) less than three times normal, Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. Patients of both genders must be willing to practice effective birth control during this trial because the potential for teratogenic effects are unknown. Patients may have had prior adjuvant treatment with immunotherapy, including interferon, as long as 3 weeks have elapsed since prior systemic therapy. EXCLUSION CRITERIA: Patients will be excluded: Who have ocular or mucosal melanoma. Who are undergoing or have undergone in the past 3 weeks any systemic therapy except surgery for their cancer, and must have recovered to a grade I from any adverse effects of treatment prior to entry, other than those that do not have clinical implications, e.g. vitiligo, alopecia. Have active systemic infections, autoimmune disease or any known immunodeficiency disease. Who require systemic steroid therapy. Who are pregnant (because of possible side effects on the fetus) or breastfeeding because of unknown effects on the developing child). Who are known to be positive for hepatitis BsAG or human immunodeficiency virus (HIV) antibody (because of possible immune effects of these conditions). Who have any form of autoimmune disease (such as autoimmune colitis or Crohn's Disease) or immunodeficiency as evidenced by abnormal white blood count (WBC) count 8 and/or presence of opportunistic infections. Must have recovered immune competence after radiation therapy. (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 have previously been immunized with gp100. Who have known hypersensitivity to any of the agents used in this study. Who have previously received chemotherapy for treatment of melanoma. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | National Cancer Institute (NCI) | Bethesda | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| National Cancer Institute (NCI) |
United States,
Kawakami Y, Eliyahu S, Delgado CH, Robbins PF, Rivoltini L, Topalian SL, Miki T, Rosenberg SA. Cloning of the gene coding for a shared human melanoma antigen recognized by autologous T cells infiltrating into tumor. Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3515-9. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Immunologic Response Rate | Comparison of six different preparations of the gp100:209-217 (210M) melanoma antigen peptide. The arm with the greater number of immunologic responses will be the one most likely to be selected for future study on the basis of immunization alone. Evidence of immunization consist of at least 10 Elispots/100,000 cells above background. An injection site reaction is not an immune response. | 48 months | No |
| Secondary | Number of Participants With Adverse Events | Here are the number of participants with adverse events. For a detailed list of adverse events see the adverse event module. | 48 months | Yes |