Clinical and immunological evaluation of patients with metastatic melanoma undergoing immunization with the HLA-Cw*0702-associated epitope MAGE-A12:170-178

Int J Cancer. 2003 Jun 10;105(2):210-6. doi: 10.1002/ijc.11045.

Abstract

Patients with metastatic melanoma who expressed HLA-Cw*0702 and whose tumors had demonstrable MAGE-A12 expression were immunized with the peptide MAGE-A12:170-178 administered subcutaneously in incomplete Freund's adjuvant (IFA). The peptide was administered either every week or every 3 weeks for 4 cycles. Patients were evaluated for toxicity and for immunologic and clinical response to peptide immunization. Pre-treatment fine needle aspirates were obtained to document MAGE-A12 expression for enrollment. MAGE-A12 mRNA was identified in 62% of specimens. Nine patients were selected for vaccination based on MAGE-A12 expression and the presence of HLA-Cw*0702. The immune response was monitored both by tetrameric HLA-Cw*0702/MAGE-A12:170-178 complexes and by analysis of interferon-gamma mRNA transcription using a quantitative real-time polymerase chain reaction assay after peptide-specific stimulation. The samples consisted of circulating lymphocytes analyzed ex vivo or after 10 to 14 days of in vitro sensitization. One of 9 patients sustained an ongoing partial clinical response. No convincing evidence of enhancement of the systemic immune response against MAGE-A12:170-178 could be documented. Because of the modest immunological and clinical results, the present protocol has been discontinued as new routes of administration are being considered.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology*
  • Cancer Vaccines / therapeutic use*
  • Case-Control Studies
  • Cells, Cultured
  • DNA Primers / chemistry
  • Female
  • HLA-C Antigens / immunology*
  • Humans
  • Immunity, Cellular
  • Immunization*
  • Immunotherapy
  • Interferon-gamma / genetics
  • Male
  • Melanoma / genetics
  • Melanoma / immunology*
  • Melanoma / secondary
  • Melanoma / therapy
  • Middle Aged
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / immunology*
  • Peptide Fragments / genetics
  • Peptide Fragments / immunology
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Skin Neoplasms / genetics
  • Skin Neoplasms / immunology*
  • Skin Neoplasms / pathology
  • Skin Neoplasms / therapy
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Cytotoxic / metabolism*
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • Antigens, Neoplasm
  • Cancer Vaccines
  • DNA Primers
  • HLA-C Antigens
  • MAGEA12 protein, human
  • Neoplasm Proteins
  • Peptide Fragments
  • RNA, Messenger
  • Interferon-gamma