Neoadjuvant personalized cancer vaccines: the final frontier?

ABSTRACTIntroduction Clinical trials of personalized cancer vaccines have shown that on-demand therapies that are manufactured for each patient, result in activated T cell responses against individual tumor neoantigens. However, their use has been traditionally restricted to adjuvant settings and la...

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Main Authors: Guilhem Richard, Nicole Ruggiero, Gary D. Steinberg, William D. Martin, Anne S. De Groot
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Expert Review of Vaccines
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/14760584.2024.2303015
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author Guilhem Richard
Nicole Ruggiero
Gary D. Steinberg
William D. Martin
Anne S. De Groot
author_facet Guilhem Richard
Nicole Ruggiero
Gary D. Steinberg
William D. Martin
Anne S. De Groot
author_sort Guilhem Richard
collection DOAJ
description ABSTRACTIntroduction Clinical trials of personalized cancer vaccines have shown that on-demand therapies that are manufactured for each patient, result in activated T cell responses against individual tumor neoantigens. However, their use has been traditionally restricted to adjuvant settings and late-stage cancer therapy. There is growing support for the implementation of PCV earlier in the cancer therapy timeline, for reasons that will be discussed in this review.Areas covered The efficacy of cancer vaccines may be to some extent dependent on treatment(s) given prior to vaccine administration. Tumors can undergo radical immunoediting following treatment with immunotherapies, such as checkpoint inhibitors, which may affect the presence of the very mutations targeted by cancer vaccines. This review will cover the topics of neoantigen cancer vaccines, tumor immunoediting, and therapy timing.Expert opinion Therapy timing remains a critical topic to address in optimizing the efficacy of personalized cancer vaccines. Most personalized cancer vaccines are being evaluated in late-stage cancer patients and after treatment with checkpoint inhibitors, but they may offer a greater benefit to the patient if administered in earlier clinical settings, such as the neoadjuvant setting, where patients are not facing T cell exhaustion and/or a further compromised immune system.
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spelling doaj.art-c49a5329643540508e3c44e5426a9e1f2024-01-10T19:09:08ZengTaylor & Francis GroupExpert Review of Vaccines1476-05841744-83952024-12-0123120521210.1080/14760584.2024.2303015Neoadjuvant personalized cancer vaccines: the final frontier?Guilhem Richard0Nicole Ruggiero1Gary D. Steinberg2William D. Martin3Anne S. De Groot4EpiVax Therapeutics, Inc., Providence, RI, USAEpiVax Therapeutics, Inc., Providence, RI, USAEpiVax Therapeutics, Inc., Providence, RI, USAEpiVax, Inc., Providence, RI, USAEpiVax, Inc., Providence, RI, USAABSTRACTIntroduction Clinical trials of personalized cancer vaccines have shown that on-demand therapies that are manufactured for each patient, result in activated T cell responses against individual tumor neoantigens. However, their use has been traditionally restricted to adjuvant settings and late-stage cancer therapy. There is growing support for the implementation of PCV earlier in the cancer therapy timeline, for reasons that will be discussed in this review.Areas covered The efficacy of cancer vaccines may be to some extent dependent on treatment(s) given prior to vaccine administration. Tumors can undergo radical immunoediting following treatment with immunotherapies, such as checkpoint inhibitors, which may affect the presence of the very mutations targeted by cancer vaccines. This review will cover the topics of neoantigen cancer vaccines, tumor immunoediting, and therapy timing.Expert opinion Therapy timing remains a critical topic to address in optimizing the efficacy of personalized cancer vaccines. Most personalized cancer vaccines are being evaluated in late-stage cancer patients and after treatment with checkpoint inhibitors, but they may offer a greater benefit to the patient if administered in earlier clinical settings, such as the neoadjuvant setting, where patients are not facing T cell exhaustion and/or a further compromised immune system.https://www.tandfonline.com/doi/10.1080/14760584.2024.2303015Checkpoint inhibitorimmunoinformaticsimmunotherapypersonalized cancer vaccineneoadjuvant therapyneoantigen
spellingShingle Guilhem Richard
Nicole Ruggiero
Gary D. Steinberg
William D. Martin
Anne S. De Groot
Neoadjuvant personalized cancer vaccines: the final frontier?
Expert Review of Vaccines
Checkpoint inhibitor
immunoinformatics
immunotherapy
personalized cancer vaccine
neoadjuvant therapy
neoantigen
title Neoadjuvant personalized cancer vaccines: the final frontier?
title_full Neoadjuvant personalized cancer vaccines: the final frontier?
title_fullStr Neoadjuvant personalized cancer vaccines: the final frontier?
title_full_unstemmed Neoadjuvant personalized cancer vaccines: the final frontier?
title_short Neoadjuvant personalized cancer vaccines: the final frontier?
title_sort neoadjuvant personalized cancer vaccines the final frontier
topic Checkpoint inhibitor
immunoinformatics
immunotherapy
personalized cancer vaccine
neoadjuvant therapy
neoantigen
url https://www.tandfonline.com/doi/10.1080/14760584.2024.2303015
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