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Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors
The three major standard therapies, that is, surgery, chemotherapy, and radiation therapy have conventionally been applied to the treatments for cancers and have saved many patients. In addition, for intractable, refractory, or advanced malignancies that cannot be cured by the three standard therapi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746052/ https://www.ncbi.nlm.nih.gov/pubmed/36047968 http://dx.doi.org/10.1111/cas.15552 |
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author | Adachi, Keishi Tamada, Koji |
author_facet | Adachi, Keishi Tamada, Koji |
author_sort | Adachi, Keishi |
collection | PubMed |
description | The three major standard therapies, that is, surgery, chemotherapy, and radiation therapy have conventionally been applied to the treatments for cancers and have saved many patients. In addition, for intractable, refractory, or advanced malignancies that cannot be cured by the three standard therapies, immunotherapy is an important subject of basic and clinical researches. Immune checkpoint inhibitor therapy (ICI) has shown significant therapeutic efficacies on some types of tumors in large‐scale randomized clinical trials, making a major impact on clinical oncology by scientifically proving and establishing the effectiveness of an immunotherapy. In 2018, ICI was awarded the Nobel Prize in Physiology or Medicine, and immunotherapy is now becoming the “fourth” standard therapy for cancers. Recently, adoptive cell therapies, in which genetically modified T cells with enhanced reactivity against tumors are infused into the patients, have been attracting considerable attention as a hopeful immunotherapy following ICI. Particularly, chimeric antigen receptor (CAR)‐T‐cell therapies demonstrate marked therapeutic efficacies against some hematologic malignancies, and have been approved in many countries. However, current CAR‐T‐cell therapy is considered to be little effective against solid tumors, which is one of the challenging issues to be overcome in CAR‐T‐cell therapy. In this review, we at first introduce CAR and CAR‐T cell, and then focus on the recent progress of CAR‐T‐cell therapy against solid tumors as well as the novel concept on a role of CAR‐T cells, aiming to further understandings of the novel cancer immunotherapies. |
format | Online Article Text |
id | pubmed-9746052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97460522022-12-14 Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors Adachi, Keishi Tamada, Koji Cancer Sci Review Articles The three major standard therapies, that is, surgery, chemotherapy, and radiation therapy have conventionally been applied to the treatments for cancers and have saved many patients. In addition, for intractable, refractory, or advanced malignancies that cannot be cured by the three standard therapies, immunotherapy is an important subject of basic and clinical researches. Immune checkpoint inhibitor therapy (ICI) has shown significant therapeutic efficacies on some types of tumors in large‐scale randomized clinical trials, making a major impact on clinical oncology by scientifically proving and establishing the effectiveness of an immunotherapy. In 2018, ICI was awarded the Nobel Prize in Physiology or Medicine, and immunotherapy is now becoming the “fourth” standard therapy for cancers. Recently, adoptive cell therapies, in which genetically modified T cells with enhanced reactivity against tumors are infused into the patients, have been attracting considerable attention as a hopeful immunotherapy following ICI. Particularly, chimeric antigen receptor (CAR)‐T‐cell therapies demonstrate marked therapeutic efficacies against some hematologic malignancies, and have been approved in many countries. However, current CAR‐T‐cell therapy is considered to be little effective against solid tumors, which is one of the challenging issues to be overcome in CAR‐T‐cell therapy. In this review, we at first introduce CAR and CAR‐T cell, and then focus on the recent progress of CAR‐T‐cell therapy against solid tumors as well as the novel concept on a role of CAR‐T cells, aiming to further understandings of the novel cancer immunotherapies. John Wiley and Sons Inc. 2022-09-13 2022-12 /pmc/articles/PMC9746052/ /pubmed/36047968 http://dx.doi.org/10.1111/cas.15552 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 | Review Articles Adachi, Keishi Tamada, Koji Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors |
title | Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors |
title_full | Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors |
title_fullStr | Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors |
title_full_unstemmed | Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors |
title_short | Paving the road to make chimeric antigen receptor‐T‐cell therapy effective against solid tumors |
title_sort | paving the road to make chimeric antigen receptor‐t‐cell therapy effective against solid tumors |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746052/ https://www.ncbi.nlm.nih.gov/pubmed/36047968 http://dx.doi.org/10.1111/cas.15552 |
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