Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment
Endometrial cancer (EC), while generally curable in early stages, poses significant challenges when it recurs or advances. Recent advancements in immunotherapy, specifically immune checkpoint inhibitors, have provided a promising therapeutic option for such cases, especially with FDA-approved drugs...
| Authors: | , , , , |
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| Format: | article |
| Status: | Published version |
| Publication Date: | 2024 |
| Country: | España |
| Institution: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repository: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10459.1/467181 |
| Online Access: | https://doi.org/10.3390/cancers16233918 https://hdl.handle.net/10459.1/467181 |
| Access Level: | Open access |
| Keyword: | Endometrial cancer Immunotherapy Mismatch repair Tumor mutational burden Tumor microenvironment Immune checkpoint blockade Cell-based therapies |
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Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor MicroenvironmentAlbertí Valls, ManelOlave, SaraOlomí, AnnaMacià Armengol, AnnaEritja Sánchez, NúriaEndometrial cancerImmunotherapyMismatch repairTumor mutational burdenTumor microenvironmentImmune checkpoint blockadeCell-based therapiesEndometrial cancer (EC), while generally curable in early stages, poses significant challenges when it recurs or advances. Recent advancements in immunotherapy, specifically immune checkpoint inhibitors, have provided a promising therapeutic option for such cases, especially with FDA-approved drugs like pembrolizumab, durvalumab, and dostarlimab. The molecular classification of EC, particularly mismatch repair deficiency, has proven essential in identifying tumors that are likely to respond to immune checkpoint inhibitors, owing to their increased tumor mutational burden and higher PD-L1 expression. However, mismatch repair (MMR) status alone is insufficient to predict immune responses as treatment outcomes are also substantially influenced by tumor microenvironment composition, immune infiltration, and inter-individual variability. Emerging cell therapies like Chimeric Antigen Receptor (CAR) T cells and tumor-infiltrating lymphocytes offer hope for addressing non-immunogenic tumors, overcoming immune evasion mechanisms that limit natural immune responses.This work has been funded by the Instituto de Salud Carlos III (ISCIII) through the projects PI20/00502, CP19/00025, CB16/12/00231, Cofounded by European Regional Development Fund (ERDF) ‘a way to make Europe’ and ESF ‘Investing in your future’) and the Fundación Contigo Contra el Cáncer de la Mujer. We also thank the grups consolidats de la Generalitat de Catalunya (2021SGR00093). M.A.-V. holds a predoctoral fellowship from the Universitat de Lleida.MDPI2024info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://doi.org/10.3390/cancers16233918https://hdl.handle.net/10459.1/467181reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a https://doi.org/10.3390/cancers16233918Cancers, 2024, vol. 16, núm. 3918.cc-by, (c) Albertí et al., 2024Attribution 4.0 Internationalinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/oai:recercat.cat:10459.1/4671812026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| title |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| spellingShingle |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment Albertí Valls, Manel Endometrial cancer Immunotherapy Mismatch repair Tumor mutational burden Tumor microenvironment Immune checkpoint blockade Cell-based therapies |
| title_short |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| title_full |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| title_fullStr |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| title_full_unstemmed |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| title_sort |
Advances in Immunotherapy for Endometrial Cancer: Insights into MMR Status and Tumor Microenvironment |
| dc.creator.none.fl_str_mv |
Albertí Valls, Manel Olave, Sara Olomí, Anna Macià Armengol, Anna Eritja Sánchez, Núria |
| author |
Albertí Valls, Manel |
| author_facet |
Albertí Valls, Manel Olave, Sara Olomí, Anna Macià Armengol, Anna Eritja Sánchez, Núria |
| author_role |
author |
| author2 |
Olave, Sara Olomí, Anna Macià Armengol, Anna Eritja Sánchez, Núria |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Endometrial cancer Immunotherapy Mismatch repair Tumor mutational burden Tumor microenvironment Immune checkpoint blockade Cell-based therapies |
| topic |
Endometrial cancer Immunotherapy Mismatch repair Tumor mutational burden Tumor microenvironment Immune checkpoint blockade Cell-based therapies |
| description |
Endometrial cancer (EC), while generally curable in early stages, poses significant challenges when it recurs or advances. Recent advancements in immunotherapy, specifically immune checkpoint inhibitors, have provided a promising therapeutic option for such cases, especially with FDA-approved drugs like pembrolizumab, durvalumab, and dostarlimab. The molecular classification of EC, particularly mismatch repair deficiency, has proven essential in identifying tumors that are likely to respond to immune checkpoint inhibitors, owing to their increased tumor mutational burden and higher PD-L1 expression. However, mismatch repair (MMR) status alone is insufficient to predict immune responses as treatment outcomes are also substantially influenced by tumor microenvironment composition, immune infiltration, and inter-individual variability. Emerging cell therapies like Chimeric Antigen Receptor (CAR) T cells and tumor-infiltrating lymphocytes offer hope for addressing non-immunogenic tumors, overcoming immune evasion mechanisms that limit natural immune responses. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
| dc.identifier.none.fl_str_mv |
https://doi.org/10.3390/cancers16233918 https://hdl.handle.net/10459.1/467181 |
| url |
https://doi.org/10.3390/cancers16233918 https://hdl.handle.net/10459.1/467181 |
| dc.language.none.fl_str_mv |
Inglés |
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Inglés |
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Reproducció del document publicat a https://doi.org/10.3390/cancers16233918 Cancers, 2024, vol. 16, núm. 3918. |
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cc-by, (c) Albertí et al., 2024 Attribution 4.0 International info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ |
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cc-by, (c) Albertí et al., 2024 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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MDPI |
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MDPI |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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