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Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era

Since pembrolizumab, an anti-programmed death-1 (PD-1) antibody, showed a dramatic response to immunogenic cancers with microsatellite instability-high (MSI-H) and/or deficient mismatch repair (dMMR) in the pilot clinical trial KEYNOTE-016, subsequent studies have confirmed durable responses of anti...

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Detalles Bibliográficos
Autores principales: Shimozaki, Keitaro, Nakayama, Izuma, Hirota, Toru, Yamaguchi, Kensei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093684/
https://www.ncbi.nlm.nih.gov/pubmed/37048122
http://dx.doi.org/10.3390/cells12071049
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author Shimozaki, Keitaro
Nakayama, Izuma
Hirota, Toru
Yamaguchi, Kensei
author_facet Shimozaki, Keitaro
Nakayama, Izuma
Hirota, Toru
Yamaguchi, Kensei
author_sort Shimozaki, Keitaro
collection PubMed
description Since pembrolizumab, an anti-programmed death-1 (PD-1) antibody, showed a dramatic response to immunogenic cancers with microsatellite instability-high (MSI-H) and/or deficient mismatch repair (dMMR) in the pilot clinical trial KEYNOTE-016, subsequent studies have confirmed durable responses of anti-PD-1 inhibitors for MSI-H/dMMR solid tumors. As immunotherapy is described as a “game changer,” the therapeutic landscape for MSI-H/dMMR solid tumors including gastrointestinal cancers has changed considerably in the last decade. An MSI/MMR status has been established as the predictive biomarker for immune checkpoint blockades, playing an indispensable role in the clinical practice of patients with MSI-H/dMMR tumors. Immunotherapy is also now investigated for locally advanced MSI-H/dMMR gastrointestinal cancers. Despite this great success, a few populations with MSI-H/dMMR gastrointestinal cancers do not respond to immunotherapy, possibly due to the existence of intrinsic or acquired resistance mechanisms. Clarifying the underlying mechanisms of resistance remains a future task, whereas attempts to overcome resistance and improve the efficacy of immunotherapy are currently ongoing. Herein, we review recent clinical trials with special attention to MSI-H/dMMR gastrointestinal cancers together with basic/translational findings, which provide their rationale, and discuss perspectives for the further therapeutic development of treatment in this field.
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spelling pubmed-100936842023-04-13 Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era Shimozaki, Keitaro Nakayama, Izuma Hirota, Toru Yamaguchi, Kensei Cells Review Since pembrolizumab, an anti-programmed death-1 (PD-1) antibody, showed a dramatic response to immunogenic cancers with microsatellite instability-high (MSI-H) and/or deficient mismatch repair (dMMR) in the pilot clinical trial KEYNOTE-016, subsequent studies have confirmed durable responses of anti-PD-1 inhibitors for MSI-H/dMMR solid tumors. As immunotherapy is described as a “game changer,” the therapeutic landscape for MSI-H/dMMR solid tumors including gastrointestinal cancers has changed considerably in the last decade. An MSI/MMR status has been established as the predictive biomarker for immune checkpoint blockades, playing an indispensable role in the clinical practice of patients with MSI-H/dMMR tumors. Immunotherapy is also now investigated for locally advanced MSI-H/dMMR gastrointestinal cancers. Despite this great success, a few populations with MSI-H/dMMR gastrointestinal cancers do not respond to immunotherapy, possibly due to the existence of intrinsic or acquired resistance mechanisms. Clarifying the underlying mechanisms of resistance remains a future task, whereas attempts to overcome resistance and improve the efficacy of immunotherapy are currently ongoing. Herein, we review recent clinical trials with special attention to MSI-H/dMMR gastrointestinal cancers together with basic/translational findings, which provide their rationale, and discuss perspectives for the further therapeutic development of treatment in this field. MDPI 2023-03-30 /pmc/articles/PMC10093684/ /pubmed/37048122 http://dx.doi.org/10.3390/cells12071049 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Shimozaki, Keitaro
Nakayama, Izuma
Hirota, Toru
Yamaguchi, Kensei
Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era
title Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era
title_full Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era
title_fullStr Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era
title_full_unstemmed Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era
title_short Current Strategy to Treat Immunogenic Gastrointestinal Cancers: Perspectives for a New Era
title_sort current strategy to treat immunogenic gastrointestinal cancers: perspectives for a new era
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10093684/
https://www.ncbi.nlm.nih.gov/pubmed/37048122
http://dx.doi.org/10.3390/cells12071049
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