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This is an Open-label, Phase II Study of a Vaccine Comprising Melanoma Peptides and a Tetanus Helper Peptide, Administered in GM-CSF-in-adjuvant. Patients Will be Randomized to Receive One of Two Different Vaccine Regimens. Patients Will be Stratified by Stage of Disease (IIB vs. III vs. IV).

Phase 2
18 Years
85 Years
Open (Enrolling)

Thank you

Trial Information

This is an Open-label, Phase II Study of a Vaccine Comprising Melanoma Peptides and a Tetanus Helper Peptide, Administered in GM-CSF-in-adjuvant. Patients Will be Randomized to Receive One of Two Different Vaccine Regimens. Patients Will be Stratified by Stage of Disease (IIB vs. III vs. IV).

Each vaccination will be administered over a 6-week period (days 1, 8, 15, 29, 36, 43).
Patients will be randomized into one of two groups, Group A or Group B.

Group A will receive 4 class I MHC-restricted synthetic melanoma peptides (1 each restricted
by HLA-A1, -A3, and two restricted by HLA-A2) and a tetanus helper peptide.

Group B will receive the 12 class I MHC-restricted synthetic melanoma peptides (4 each
restricted to HLA-A1, -A2, and -A3) and a tetanus helper peptide.

All vaccines will contain GM-CSF-in-adjuvant and will be administered intradermally and
subcutaneously. Concurrent with the first three of these vaccinations, each patient will
also receive an additional set of 3 identical vaccinations in a distal site, the response to
which will be evaluated at the draining lymph node. This node will be harvested using
lymphatic mapping and sentinel node biopsy methods and will be referred to as the sentinel
immunized node (SIN).

Inclusion Criteria:

- Patients who have been diagnosed, by cytologic or histologic examination, with
resected AJCC stage IIB, stage III, or stage IV cutaneous or mucosal melanoma.

- Patients who have had brain metastases will be eligible if (a) they have been
resected surgically, or (b) there have been 1-3 brain metastases less than or equal
to 2 cm that have been treated with the gamma-knife or stereotactic radiosurgery.
Surgical resections or gamma-knife must have been completed no greater than 10 months
prior to study entry.

- Tumor must express either gp100 (for patients HLA-A2+ or HLA-A3+) or tyrosinase (for
patients HLA-A1+ or HLA-A2+) by immunohistochemistry. The tumor deposit(s) to be
examined will be the primary lesion for stage IIB patients, or the most recently
resected metastatic disease in stage III or stage IV patients. If the most recently
resected deposit is not available than material from prior resected tumor will be

- Patients who refuse treatment with IFN-alpha despite being candidates for IFN-alpha.

- Patients who are not eligible for treatment with IFN-alpha for the following reasons:

- active ischemic heart disease or cerebro-vascular disease,

- anginal syndrome requiring ongoing medications, or history of myocardial
infarction, or arrhythmia disorder,

- history of treatment for depression or active depression, or other psychiatric

- patients with autoimmune disorders who are not excluded based on criteria listed
in section 5.2.8 of the present study,

- patients in whom greater than 6 months have elapsed since their definitive
surgical therapy,

- hypersensitivity to IFN-alpha or any component associated with the treatment,

- debilitating medical conditions such as severe pulmonary disease or severe
diabetes mellitus,

- patients with thyroid abnormalities whose thyroid function cannot be maintained
in the normal range without medication

- patients with resected stage IV disease provided they meet the eligibility
criteria for the proposed study,

- patients who discontinue IFN-alpha therapy due to the occurrence of a major
toxicity that has been documented by their treating physician,

- patients who have undergone IFN-alpha therapy and have experienced tumor
progression while on IFN or after completing IFN.

- All patients must have:

- Karnofsky performance of 80% or higher,

- ECOG performance status of 0 or 1,

- Ability and willingness to give informed consent.

- Laboratory parameters as follows:

- HLA-A1, -A2, or -A3 (+),

- ANC > 1000/mm3, and Platelets > 100,000 and Hgb > 9,

- Hepatic: AST and ALT up to 2.5 x upper limits of normal (ULN), Bilirubin up to
2.5 x ULN, Alkaline phosphatase up to 2.5 x ULN,

- Renal: Creatinine up to 1.5 x ULN,

- Serology: HIV negative and Hepatitis C negative within 6 months of study entry,

- LDH up to 1.5 x ULN.

- Age 18 years or older at the time of study entry.

Exclusion Criteria:

- Patients with ocular melanoma.

- Patients who are currently receiving cytotoxic chemotherapy, interferon, or radiation
or who have received this therapy within the preceding 4 weeks.

- Patients who are currently receiving nitrosoureas or who have received this therapy
within the preceding 6 weeks.

- Patients with known or suspected allergies to any component of the vaccine.

- Patients receiving the following medications at study entry or within the preceding 4
weeks are excluded: Agents with putative immunomodulating activity (with the
exception of non-steroidal anti-inflammatory agents), Allergy desensitization
injections, Corticosteroids, administered parenterally or orally. Topical
corticosteroids are acceptable. Any growth factors, Interleukin-2 or other

- Prior melanoma vaccinations will be an exclusion criteria. However, those patients
who have recurred either after or during administration of a melanoma vaccine will be
eligible to enroll 12 weeks following their last vaccination.

- Patients may not have been vaccinated previously with any of the peptides that are
included in this protocol. Other investigational drugs or investigational therapy
will not necessarily be an exclusion criteria, but will similarly be recorded and
taken into account during data analysis.

- Pregnancy or the possibility of becoming pregnant during vaccine administration.
Female patients of childbearing potential must have a negative pregnancy test
(urinary or serum beta-HCG) prior to administration of the first vaccine dose. Males
and females must agree, in the consent form, to use effective birth control methods
during the course of vaccination. This is consistent with existing standards of
practice for vaccine and chemotherapy protocols.

- Patients in whom there is a medical contraindication or potential problem in
complying with the requirements of the protocol, in the opinion of the investigator.

- Patients classified according to the New York Heart Association classification as
having Class III, or IV heart disease.

- Patients who have systemic autoimmune disease with visceral involvement.

- Patients who have another cancer diagnosis, except that the following diagnoses will
be allowed: squamous cell cancer of the skin without known metastasis, basal cell
cancer of the skin without known metastasis, carcinoma in situ of the breast (DCIS or
LCIS), carcinoma in situ of the cervix, any cancer without distant metastasis that
has been treated successfully, without evidence of recurrence or metastasis for over
5 years.

- Patients with known addiction to alcohol or drugs who is actively taking those
agents, or patients with recent (within 1 year) or ongoing illicit IV drug use.

Type of Study:


Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Safety of the 12-peptide mixture and cumulative number of T cells derived from the sentinel immunized node that are reactive to the 12 melanoma peptides included in the vaccine, in the context of HLA-A1, -A2, or -A3.

Outcome Time Frame:

24 months

Safety Issue:


Principal Investigator

Craig L Slingluff, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of Virginia


United States: Food and Drug Administration

Study ID:




Start Date:

August 2000

Completion Date:

Related Keywords:

  • Melanoma
  • melanoma
  • peptide
  • vaccine
  • adjuvant
  • advanced
  • Melanoma



University of Virginia Charlottesville, Virginia  22908