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Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines

The present study assessed plasma IgG in patients with metastatic recurrent breast cancer (mrBC) that is reactive to various T-cell epitope peptides of prostate-related antigens (PRAs), such as prostate-specific antigen, prostate-specific membrane antigen and prostate acid phosphatase. Patients were...

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Autores principales: Saku, Shuko, Toh, Uhi, Takao, Yuko, Sakurai, Sayaka, Yamada, Akira, Shichijo, Shigeki, Itoh, Kyogo, Akagi, Yoshito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264823/
https://www.ncbi.nlm.nih.gov/pubmed/34249152
http://dx.doi.org/10.3892/etm.2021.10337
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author Saku, Shuko
Toh, Uhi
Takao, Yuko
Sakurai, Sayaka
Yamada, Akira
Shichijo, Shigeki
Itoh, Kyogo
Akagi, Yoshito
author_facet Saku, Shuko
Toh, Uhi
Takao, Yuko
Sakurai, Sayaka
Yamada, Akira
Shichijo, Shigeki
Itoh, Kyogo
Akagi, Yoshito
author_sort Saku, Shuko
collection PubMed
description The present study assessed plasma IgG in patients with metastatic recurrent breast cancer (mrBC) that is reactive to various T-cell epitope peptides of prostate-related antigens (PRAs), such as prostate-specific antigen, prostate-specific membrane antigen and prostate acid phosphatase. Patients were treated with personalized peptide vaccines (PPVs) which were selected and administered from a panel of candidate peptides based on human leukocyte antigen-types and prevaccination IgG levels to each peptide. The peptide panel consisted of 27 cytotoxic T-lymphocyte-epitope peptides derived from tumor-associated antigens, not including PRA. PRA peptides and peptide panels were retrospectively analyzed in 77 PPV-treated patients. The results revealed that PRA reactive IgG levels were increased after vaccination in 31 of the 97 patients included in the present study. Although there was no significant association between anti-PRA peptide levels and progression-free survival (PFS) or overall survival, anti-PRA peptide levels were significantly associated with PFS (P=0.009) in estrogen-receptor positive (ER+) patients with cancer. The results suggested that plasma anti-PRA IgG levels may be a useful prognostic marker for monitoring PPVs, particularly for ER+ patients with mrBC (trial registration no. from the UMIN Clinical Trials Registry, UMIN000001844).
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spelling pubmed-82648232021-07-09 Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines Saku, Shuko Toh, Uhi Takao, Yuko Sakurai, Sayaka Yamada, Akira Shichijo, Shigeki Itoh, Kyogo Akagi, Yoshito Exp Ther Med Articles The present study assessed plasma IgG in patients with metastatic recurrent breast cancer (mrBC) that is reactive to various T-cell epitope peptides of prostate-related antigens (PRAs), such as prostate-specific antigen, prostate-specific membrane antigen and prostate acid phosphatase. Patients were treated with personalized peptide vaccines (PPVs) which were selected and administered from a panel of candidate peptides based on human leukocyte antigen-types and prevaccination IgG levels to each peptide. The peptide panel consisted of 27 cytotoxic T-lymphocyte-epitope peptides derived from tumor-associated antigens, not including PRA. PRA peptides and peptide panels were retrospectively analyzed in 77 PPV-treated patients. The results revealed that PRA reactive IgG levels were increased after vaccination in 31 of the 97 patients included in the present study. Although there was no significant association between anti-PRA peptide levels and progression-free survival (PFS) or overall survival, anti-PRA peptide levels were significantly associated with PFS (P=0.009) in estrogen-receptor positive (ER+) patients with cancer. The results suggested that plasma anti-PRA IgG levels may be a useful prognostic marker for monitoring PPVs, particularly for ER+ patients with mrBC (trial registration no. from the UMIN Clinical Trials Registry, UMIN000001844). D.A. Spandidos 2021-08 2021-06-25 /pmc/articles/PMC8264823/ /pubmed/34249152 http://dx.doi.org/10.3892/etm.2021.10337 Text en Copyright: © Saku et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Articles
Saku, Shuko
Toh, Uhi
Takao, Yuko
Sakurai, Sayaka
Yamada, Akira
Shichijo, Shigeki
Itoh, Kyogo
Akagi, Yoshito
Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
title Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
title_full Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
title_fullStr Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
title_full_unstemmed Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
title_short Plasma level of prostate related-antigen peptide-reactive IgG is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
title_sort plasma level of prostate related-antigen peptide-reactive igg is a prognostic factor of patients with breast cancer treated with personalized peptide vaccines
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264823/
https://www.ncbi.nlm.nih.gov/pubmed/34249152
http://dx.doi.org/10.3892/etm.2021.10337
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