Active Specific Intranodal Immunotherapy of Recombinant Vaccinia Virus in Locally Advanced to Metastatic Melanoma

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00116597
Recruitment Status : Completed
First Posted : June 30, 2005
Last Update Posted : December 2, 2009
Information provided by:
University Hospital, Basel, Switzerland

June 29, 2005
June 30, 2005
December 2, 2009
November 2002
July 2007   (Final data collection date for primary outcome measure)
  • Safety evaluation
  • Clinical response
  • Immune response assessment
Same as current
Complete list of historical versions of study NCT00116597 on Archive Site
  • Survival (disease-free survival [DFS], overall survival [OS])
  • Dose adaptation
Same as current
Not Provided
Not Provided
Active Specific Intranodal Immunotherapy of Recombinant Vaccinia Virus in Locally Advanced to Metastatic Melanoma
Active Specific Intranodal Immunotherapy With a Recombinant Vaccinia Virus Expressing Three Melanoma Associated Epitopes and Two Costimulatory Molecules, Followed by Immunization With Synthetic Melanoma Associated Epitopes. A Phase I/II Trial in Patients With Stages IIb to IV Melanoma

The purpose of this study is to assess intranodal immunotherapy in locally advanced to metastatic melanoma patients (American Joint Committee on Cancer [AJCC] stages IIb to IV).

For this, the investigators capitalize on their previous melanoma clinical trial (published by Zajac P et al in Human Gene Ther 2003) and take advantage of a proprietary recombinant vaccinia virus (replication inactivated) expressing 5 minigenes: 3 melanoma associated antigens and 2 costimulatory molecules. Immunization with the recombinant vaccinia virus is followed by 3 boosts with soluble, synthetic melanoma associated antigens.

The patients are immunized intranodally (groin lymph node) under ultrasonographic guidance in an outpatient clinic. The protocol foresees 2 cycles of immunotherapy for alternate weeks and lasts 15 weeks.

The investigators have conducted a phase I/II clinical trial based on the intradermal administration to stage III/IV melanoma patients of a recombinant vaccinia virus encoding tumor associated antigens and costimulatory epitopes for the priming of immune responses, followed by boosts with corresponding synthetic peptides (Zajac P et al in Human Gene Ther 2003). Specific cytotoxic T cells could be induced in a majority of patients following priming, but sustained responsiveness could not be maintained by peptide boosting on a long term basis. Emerging evidence supports the notion that expansion of specific T cells requires trafficking of antigen presenting cells loaded with specific determinants to lymphatic nodes, as induced, among others, by pro-inflammatory stimuli. Therefore, we now adopt the intranodal injection of the immunogenic formulations. As for the former melanoma active specific immunotherapy trial, GM-CSF is used as a supporting cytokine. The epitopes considered are expressed, either all or some of them, in over 90% of the melanomas in Western countries; namely, we immunize with Mart-1/Melan-A epitope 27-35, Gp-100 epitope 280-288 and tyrosinase epitope 1-9. As a consequence, HLA-A2 positivity is mandatory for inclusion in the trial. The 2 costimulatory molecules expressed by cells infected with our replication-incompetent recombinant vaccinia virus are B7.1 (CD80) and B7.2 (CD86).
Phase 1
Phase 2
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Genetic: Intranodal immunization with a recombinant vaccinia virus expressing 5 transgenes
  • Biological: Intranodal booster immunizations with synthetic melanoma associated epitopes
Not Provided

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
December 2008
July 2007   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients older than 18 years
  • Histologically proven melanoma in AJCC stages IIb to IV
  • Resected, recurrent or disseminated disease
  • HLA-A2.1 MHC phenotype
  • Karnofsky performance status equal or higher than 70%

Exclusion Criteria:

  • Patients younger than 18 years
  • Pregnancy or inability to perform anticonception
  • MHC phenotype other than HLA-A2.1
  • Other concurrent malignant disease
  • Estimated life expectancy of less than 6 months
  • Allergic skin diseases, including eczema, psoriasis and neurodermitis
  • Fever or active infection of the respiratory system
  • Concurrent severe cardiac or pulmonary disease (New York Heart Association [NYHA] III and IV)
  • Significant impairment of liver or kidney function (bilirubin > 30umol/l, GOT >2.5xN, GPT >2.5xN, alkaline phosphatase >2.5xN, creatinine >1.5xN adapted to the age)
  • Impairment of the immune system (leucocyte counts <3000/mm3 or granulocytes counts <1500/mm3)
  • Concurrent immunosuppressive therapy
  • Preexisting severe anemia (hemoglobin lower than 80 g/l)
  • Preexisting thrombocytopenia (platelet counts lower than 75,000/ul)
  • Ongoing chemotherapy or chemotherapy completed less than 6 weeks before enrollment in the trial
  • Any medical or psychiatric condition which, in the opinion of the treating physician or principal investigator, would unacceptably reduce the safety of the proposed treatment, would impair the delivery of treatment, or would preclude obtaining voluntary informed consent
  • Patients receiving any other concurrent investigational treatment, or any other concurrent treatment for their cancer
  • Patients who cannot avoid close contact with children less than 3 years of age or with immunocompromised household members
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Contact information is only displayed when the study is recruiting subjects
SNF grant NPF 37 4037-55151
Not Provided
Not Provided
Michel Adamina, M.D., P.D., M.Sc., University Hospital Basel
University Hospital, Basel, Switzerland
Not Provided
Principal Investigator: Michel Adamina, M.D. University Hospital, Basel, Switzerland
Study Chair: Daniel Oertli, M.D. University Hospital, Basel, Switzerland
Study Director: Michael Heberer, M.D. University Hospital, Basel, Switzerland
Principal Investigator: Giulio C Spagnoli, M.D. University Hospital, Basel, Switzerland
Principal Investigator: Walter R Marti, M.D. University Hospital, Basel, Switzerland
University Hospital, Basel, Switzerland
December 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP