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Immunotherapy in endometrial cancer: rationale, practice and perspectives
Tumor immunotherapy has attracted more and more attention nowadays, and multiple clinical trials have confirmed its effect in a variety of solid tumors. Immune checkpoint inhibitors (ICIs), cancer vaccines, adoptive cell transfer (ACT), and lymphocyte-promoting cytokines are the main immunotherapy m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207707/ https://www.ncbi.nlm.nih.gov/pubmed/34134781 http://dx.doi.org/10.1186/s40364-021-00301-z |
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author | Cao, Wenyu Ma, Xinyue Fischer, Jean Victoria Sun, Chenggong Kong, Beihua Zhang, Qing |
author_facet | Cao, Wenyu Ma, Xinyue Fischer, Jean Victoria Sun, Chenggong Kong, Beihua Zhang, Qing |
author_sort | Cao, Wenyu |
collection | PubMed |
description | Tumor immunotherapy has attracted more and more attention nowadays, and multiple clinical trials have confirmed its effect in a variety of solid tumors. Immune checkpoint inhibitors (ICIs), cancer vaccines, adoptive cell transfer (ACT), and lymphocyte-promoting cytokines are the main immunotherapy methods. Endometrial cancer (EC) is one of the most frequent tumors in women and the prognosis of recurrent or metastatic EC is poor. Since molecular classification has been applied to EC, immunotherapy for different EC subtypes (especially POLE and MSI-H) has gradually attracted attention. In this review, we focus on the expression and molecular basis of the main biomarkers in the immunotherapy of EC firstly, as well as their clinical application significance and limitations. Blocking tumor immune checkpoints is one of the most effective strategies for cancer treatment in recent years, and has now become the focus in the field of tumor research and treatment. We summarized clinical date of planned and ongoing clinical trials and introduced other common immunotherapy methods in EC, such as cancer vaccine and ACT. Hormone aberrations, metabolic syndrome (MetS) and p53 mutant and that affect the immunotherapy of endometrial cancer will also be discussed in this review. |
format | Online Article Text |
id | pubmed-8207707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82077072021-06-16 Immunotherapy in endometrial cancer: rationale, practice and perspectives Cao, Wenyu Ma, Xinyue Fischer, Jean Victoria Sun, Chenggong Kong, Beihua Zhang, Qing Biomark Res Review Tumor immunotherapy has attracted more and more attention nowadays, and multiple clinical trials have confirmed its effect in a variety of solid tumors. Immune checkpoint inhibitors (ICIs), cancer vaccines, adoptive cell transfer (ACT), and lymphocyte-promoting cytokines are the main immunotherapy methods. Endometrial cancer (EC) is one of the most frequent tumors in women and the prognosis of recurrent or metastatic EC is poor. Since molecular classification has been applied to EC, immunotherapy for different EC subtypes (especially POLE and MSI-H) has gradually attracted attention. In this review, we focus on the expression and molecular basis of the main biomarkers in the immunotherapy of EC firstly, as well as their clinical application significance and limitations. Blocking tumor immune checkpoints is one of the most effective strategies for cancer treatment in recent years, and has now become the focus in the field of tumor research and treatment. We summarized clinical date of planned and ongoing clinical trials and introduced other common immunotherapy methods in EC, such as cancer vaccine and ACT. Hormone aberrations, metabolic syndrome (MetS) and p53 mutant and that affect the immunotherapy of endometrial cancer will also be discussed in this review. BioMed Central 2021-06-16 /pmc/articles/PMC8207707/ /pubmed/34134781 http://dx.doi.org/10.1186/s40364-021-00301-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Cao, Wenyu Ma, Xinyue Fischer, Jean Victoria Sun, Chenggong Kong, Beihua Zhang, Qing Immunotherapy in endometrial cancer: rationale, practice and perspectives |
title | Immunotherapy in endometrial cancer: rationale, practice and perspectives |
title_full | Immunotherapy in endometrial cancer: rationale, practice and perspectives |
title_fullStr | Immunotherapy in endometrial cancer: rationale, practice and perspectives |
title_full_unstemmed | Immunotherapy in endometrial cancer: rationale, practice and perspectives |
title_short | Immunotherapy in endometrial cancer: rationale, practice and perspectives |
title_sort | immunotherapy in endometrial cancer: rationale, practice and perspectives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207707/ https://www.ncbi.nlm.nih.gov/pubmed/34134781 http://dx.doi.org/10.1186/s40364-021-00301-z |
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