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Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer
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 immunolo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980387/ https://www.ncbi.nlm.nih.gov/pubmed/29473265 http://dx.doi.org/10.1111/cas.13547 |
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author | Kawamura, Junichiro Sugiura, Fumiaki Sukegawa, Yasushi Yoshioka, Yasumasa Hida, Jin‐ichi Hazama, Shoichi Okuno, Kiyotaka |
author_facet | Kawamura, Junichiro Sugiura, Fumiaki Sukegawa, Yasushi Yoshioka, Yasumasa Hida, Jin‐ichi Hazama, Shoichi Okuno, Kiyotaka |
author_sort | Kawamura, Junichiro |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5980387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59803872018-06-06 Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer Kawamura, Junichiro Sugiura, Fumiaki Sukegawa, Yasushi Yoshioka, Yasumasa Hida, Jin‐ichi Hazama, Shoichi Okuno, Kiyotaka Cancer Sci Original Articles 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. John Wiley and Sons Inc. 2018-03-31 2018-05 /pmc/articles/PMC5980387/ /pubmed/29473265 http://dx.doi.org/10.1111/cas.13547 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Kawamura, Junichiro Sugiura, Fumiaki Sukegawa, Yasushi Yoshioka, Yasumasa Hida, Jin‐ichi Hazama, Shoichi Okuno, Kiyotaka Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer |
title | Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer |
title_full | Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer |
title_fullStr | Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer |
title_full_unstemmed | Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer |
title_short | Cytotoxic T lymphocyte response to peptide vaccination predicts survival in stage III colorectal cancer |
title_sort | cytotoxic t lymphocyte response to peptide vaccination predicts survival in stage iii colorectal cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980387/ https://www.ncbi.nlm.nih.gov/pubmed/29473265 http://dx.doi.org/10.1111/cas.13547 |
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