Multiple therapeutic peptide vaccines for patients with advanced gastric cancer

Yoshiyuki Fujiwara, Kaoru Okada, Takeshi Omori, Keijiro Sugimura, Hiroshi Miyata, Masayuki Ohue, Shogo Kobayashi, Hidenori Takahashi, Hiroyuki Nakano, Chie Mochizuki, Katsuji Shimizu, Masahiko Yano, Yusuke Nakamura, Masaki Mori, Yuichiro Doki

研究成果: Contribution to journalArticle査読

16 被引用数 (Scopus)

抄録

We performed a clinical trial using HLA-A24- binding peptide vaccines containing a combination of novel cancer-testis antigens and anti-angiogenic peptides for advanced gastric cancer (GC). Thirty-five GC patients who had shown resistance to the standard therapy were enrolled in this clinical trial using vaccinations with a mixture of multiple peptides derived from DEPDC1, URLC10, FoxM1, Kif20A and VEGFR1. The safety, the overall survival (OS), and the immunological responses based on an ELISPOT assay were determined to assess differences in patients who were HLA-A24-positive [24(+)] and HLA-A24-negative [24(-)]. No severe adverse effects were observed except for severe skin reactions in 4 patients. The differences in OS were not significant between patients who were 24(+) and 24(-). In the 24(+) group, patients who showed T cell responses specific to antigen peptides had a tendency towards better survival than those who showed no response, especially to the DEPDC1 peptide. The patients with local skin reactions had significantly better OS than the others. Peptide vaccine therapy was found to be safe and is expected to induce specific T cell responses in patients with advanced GC. The survival benefit of peptide vaccine monotherapy may not have been shown and further trials are needed to confirm these results.

本文言語英語
ページ(範囲)1655-1662
ページ数8
ジャーナルInternational journal of oncology
50
5
DOI
出版ステータス出版済み - 5 2017

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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