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A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment

BACKGROUND: Neoantigens are critical targets to elicit robust antitumor T-cell responses. Personalized cancer vaccines developed based on neoantigens have shown promising results by prolonging cancer patients’ overall survival (OS) for several cancer types. However, the safety and efficacy of these...

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Autores principales: Chen, Zheling, Zhang, Shanshan, Han, Ning, Jiang, Jiahong, Xu, Yunyun, Ma, Dongying, Lu, Lantian, Guo, Xiaojie, Qiu, Min, Huang, Qinxue, Wang, Huimin, Mo, Fan, Chen, Shuqing, Yang, Liu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414362/
https://www.ncbi.nlm.nih.gov/pubmed/34484187
http://dx.doi.org/10.3389/fimmu.2021.691605
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author Chen, Zheling
Zhang, Shanshan
Han, Ning
Jiang, Jiahong
Xu, Yunyun
Ma, Dongying
Lu, Lantian
Guo, Xiaojie
Qiu, Min
Huang, Qinxue
Wang, Huimin
Mo, Fan
Chen, Shuqing
Yang, Liu
author_facet Chen, Zheling
Zhang, Shanshan
Han, Ning
Jiang, Jiahong
Xu, Yunyun
Ma, Dongying
Lu, Lantian
Guo, Xiaojie
Qiu, Min
Huang, Qinxue
Wang, Huimin
Mo, Fan
Chen, Shuqing
Yang, Liu
author_sort Chen, Zheling
collection PubMed
description BACKGROUND: Neoantigens are critical targets to elicit robust antitumor T-cell responses. Personalized cancer vaccines developed based on neoantigens have shown promising results by prolonging cancer patients’ overall survival (OS) for several cancer types. However, the safety and efficacy of these vaccine modalities remains unclear in pancreatic cancer patients. METHODS: This retrospective study enrolled 7 advanced pancreatic cancer patients. Up to 20 neoantigen peptides per patient identified by our in-house pipeline iNeo-Suite were selected, manufactured and administered to these patients with low tumor mutation burden (TMB) (less than 10 mutations/Mb). Each patient received multiple doses of vaccine depending on the progression of the disease. Peripheral blood samples of each patient were collected pre- and post-vaccination for the analysis of the immunogenicity of iNeo-Vac-P01 through ELISpot assay and flow cytometry. RESULTS: No severe vaccine-related adverse effects were witnessed in patients enrolled in this study. The mean OS, OS associated with vaccine treatment and progression free survival (PFS) were reported to be 24.1, 8.3 and 3.1 months, respectively. Higher peripheral IFN-γ titer and CD4(+) or CD8(+) effector memory T cells count post vaccination were found in patients with relatively long overall survival. Remarkably, for patient P01 who had a 21-month OS associated with vaccine treatment, the abundance of antigen-specific TCR clone drastically increased from 0% to nearly 100%, indicating the potential of iNeo-Vac-P01 in inducing the activation of a specific subset of T cells to kill cancer cells. CONCLUSIONS: Neoantigen identification and selection were successfully applied to advanced pancreatic cancer patients with low TMB. As one of the earliest studies that addressed an issue in treating pancreatic cancer with personalized vaccines, it has been demonstrated that iNeo-Vac-P01, a personalized neoantigen-based peptide vaccine, could improve the currently limited clinical efficacy of pancreatic cancer. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier (NCT03645148). Registered August 24, 2018 - Retrospectively registered
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spelling pubmed-84143622021-09-04 A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment Chen, Zheling Zhang, Shanshan Han, Ning Jiang, Jiahong Xu, Yunyun Ma, Dongying Lu, Lantian Guo, Xiaojie Qiu, Min Huang, Qinxue Wang, Huimin Mo, Fan Chen, Shuqing Yang, Liu Front Immunol Immunology BACKGROUND: Neoantigens are critical targets to elicit robust antitumor T-cell responses. Personalized cancer vaccines developed based on neoantigens have shown promising results by prolonging cancer patients’ overall survival (OS) for several cancer types. However, the safety and efficacy of these vaccine modalities remains unclear in pancreatic cancer patients. METHODS: This retrospective study enrolled 7 advanced pancreatic cancer patients. Up to 20 neoantigen peptides per patient identified by our in-house pipeline iNeo-Suite were selected, manufactured and administered to these patients with low tumor mutation burden (TMB) (less than 10 mutations/Mb). Each patient received multiple doses of vaccine depending on the progression of the disease. Peripheral blood samples of each patient were collected pre- and post-vaccination for the analysis of the immunogenicity of iNeo-Vac-P01 through ELISpot assay and flow cytometry. RESULTS: No severe vaccine-related adverse effects were witnessed in patients enrolled in this study. The mean OS, OS associated with vaccine treatment and progression free survival (PFS) were reported to be 24.1, 8.3 and 3.1 months, respectively. Higher peripheral IFN-γ titer and CD4(+) or CD8(+) effector memory T cells count post vaccination were found in patients with relatively long overall survival. Remarkably, for patient P01 who had a 21-month OS associated with vaccine treatment, the abundance of antigen-specific TCR clone drastically increased from 0% to nearly 100%, indicating the potential of iNeo-Vac-P01 in inducing the activation of a specific subset of T cells to kill cancer cells. CONCLUSIONS: Neoantigen identification and selection were successfully applied to advanced pancreatic cancer patients with low TMB. As one of the earliest studies that addressed an issue in treating pancreatic cancer with personalized vaccines, it has been demonstrated that iNeo-Vac-P01, a personalized neoantigen-based peptide vaccine, could improve the currently limited clinical efficacy of pancreatic cancer. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier (NCT03645148). Registered August 24, 2018 - Retrospectively registered Frontiers Media S.A. 2021-08-13 /pmc/articles/PMC8414362/ /pubmed/34484187 http://dx.doi.org/10.3389/fimmu.2021.691605 Text en Copyright © 2021 Chen, Zhang, Han, Jiang, Xu, Ma, Lu, Guo, Qiu, Huang, Wang, Mo, Chen and Yang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Zheling
Zhang, Shanshan
Han, Ning
Jiang, Jiahong
Xu, Yunyun
Ma, Dongying
Lu, Lantian
Guo, Xiaojie
Qiu, Min
Huang, Qinxue
Wang, Huimin
Mo, Fan
Chen, Shuqing
Yang, Liu
A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment
title A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment
title_full A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment
title_fullStr A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment
title_full_unstemmed A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment
title_short A Neoantigen-Based Peptide Vaccine for Patients With Advanced Pancreatic Cancer Refractory to Standard Treatment
title_sort neoantigen-based peptide vaccine for patients with advanced pancreatic cancer refractory to standard treatment
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8414362/
https://www.ncbi.nlm.nih.gov/pubmed/34484187
http://dx.doi.org/10.3389/fimmu.2021.691605
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