Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer

Cancer Sci. 2018 May;109(5):1545-1551. doi: 10.1111/cas.13547. Epub 2018 Mar 31.

Abstract

We previously reported a phase I clinical trial of a peptide vaccine ring finger protein 43 (RNF43) and 34-kDa translocase of the outer mitochondrial membrane (TOMM34) combined with uracil-tegafur (UFT)/LV for patients with metastatic colorectal cancer (CRC), and demonstrated the safety and immunological responsiveness of this combination therapy. In this study, we evaluated vaccination-induced immune responses to clarify the survival benefit of the combination therapy as adjuvant treatment. We enrolled 44 patients initially in an HLA-masked fashion. After the disclosure of HLA, 28 patients were in the HLA-A*2402-matched and 16 were in the unmatched group. In the HLA-matched group, 14 patients had positive CTL responses specific for the RNF43 and/or TOMM34 peptides after 2 cycles of treatment and 9 had negative responses; in the HLA-unmatched group, 10 CTL responses were positive and 2 negative. In the HLA-matched group, 3-year relapse-free survival (RFS) was significantly better in the positive CTL subgroup than in the negative-response subgroup. Patients with negative vaccination-induced CTL responses showed a significant trend towards shorter RFS than those with positive responses. Moreover, in the HLA-unmatched group, the positive CTL response subgroup showed an equally good 3-year RFS as in the HLA-matched group. In conclusion, vaccination-induced CTL response to peptide vaccination could predict survival in the adjuvant setting for stage III CRC.

Keywords: adjuvant chemotherapy; clinical trial; colorectal cancer; cytotoxic T lymphocytes; peptide vaccine therapy.

Publication types

  • Clinical Trial, Phase II

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Colorectal Neoplasms / immunology
  • Colorectal Neoplasms / mortality*
  • Colorectal Neoplasms / pathology
  • DNA-Binding Proteins / immunology*
  • Double-Blind Method
  • Female
  • HLA-A24 Antigen / immunology
  • Humans
  • Male
  • Middle Aged
  • Mitochondrial Membrane Transport Proteins / immunology*
  • Mitochondrial Precursor Protein Import Complex Proteins
  • Neoplasm Staging
  • Oncogene Proteins / immunology*
  • T-Lymphocytes, Cytotoxic / immunology*
  • Ubiquitin-Protein Ligases
  • Vaccination*

Substances

  • DNA-Binding Proteins
  • HLA-A*24:02 antigen
  • HLA-A24 Antigen
  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Precursor Protein Import Complex Proteins
  • Oncogene Proteins
  • TOMM34 protein, human
  • RNF43 protein, human
  • Ubiquitin-Protein Ligases