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Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy
The treatment of metastatic urothelial carcinoma has dramatically changed over the past decade with the approval of several therapies from multiple drug classes including immune checkpoint inhibitors, targeted therapies, and antibody drug conjugates. Although next generation sequencing of urothelial...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477976/ https://www.ncbi.nlm.nih.gov/pubmed/37675102 http://dx.doi.org/10.3389/fimmu.2023.1258388 |
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author | Benjamin, David J. Hsu, Robert |
author_facet | Benjamin, David J. Hsu, Robert |
author_sort | Benjamin, David J. |
collection | PubMed |
description | The treatment of metastatic urothelial carcinoma has dramatically changed over the past decade with the approval of several therapies from multiple drug classes including immune checkpoint inhibitors, targeted therapies, and antibody drug conjugates. Although next generation sequencing of urothelial carcinoma has revealed multiple recurring mutations, only one targeted therapy has been developed and approved to date. Erdafitinib, a pan-fibroblast growth factor receptor (FGFR) inhibitor, has been approved for treating patients with select FGFR2 and FGFR3 alterations and fusions since 2019. Since then, emerging data has demonstrated efficacy of combining erdafitinib with immunotherapy in treating FGFR-altered urothelial carcinoma. Ongoing trials are evaluating the use of erdafitinib in non-muscle invasive urothelial carcinoma as well as in combination with enfortumab vedotin in the metastatic setting, while other FGFR targeted agents such as infigratinib, AZD4547, rogaratinib and pemigatinib continue to be in development. Future challenges will include strategies to overcome FGFR acquired resistance and efficacy and safety of combination therapies with erdafitinib and other FGFR targeted agents. |
format | Online Article Text |
id | pubmed-10477976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104779762023-09-06 Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy Benjamin, David J. Hsu, Robert Front Immunol Immunology The treatment of metastatic urothelial carcinoma has dramatically changed over the past decade with the approval of several therapies from multiple drug classes including immune checkpoint inhibitors, targeted therapies, and antibody drug conjugates. Although next generation sequencing of urothelial carcinoma has revealed multiple recurring mutations, only one targeted therapy has been developed and approved to date. Erdafitinib, a pan-fibroblast growth factor receptor (FGFR) inhibitor, has been approved for treating patients with select FGFR2 and FGFR3 alterations and fusions since 2019. Since then, emerging data has demonstrated efficacy of combining erdafitinib with immunotherapy in treating FGFR-altered urothelial carcinoma. Ongoing trials are evaluating the use of erdafitinib in non-muscle invasive urothelial carcinoma as well as in combination with enfortumab vedotin in the metastatic setting, while other FGFR targeted agents such as infigratinib, AZD4547, rogaratinib and pemigatinib continue to be in development. Future challenges will include strategies to overcome FGFR acquired resistance and efficacy and safety of combination therapies with erdafitinib and other FGFR targeted agents. Frontiers Media S.A. 2023-08-22 /pmc/articles/PMC10477976/ /pubmed/37675102 http://dx.doi.org/10.3389/fimmu.2023.1258388 Text en Copyright © 2023 Benjamin and Hsu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Benjamin, David J. Hsu, Robert Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy |
title | Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy |
title_full | Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy |
title_fullStr | Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy |
title_full_unstemmed | Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy |
title_short | Treatment approaches for FGFR-altered urothelial carcinoma: targeted therapies and immunotherapy |
title_sort | treatment approaches for fgfr-altered urothelial carcinoma: targeted therapies and immunotherapy |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477976/ https://www.ncbi.nlm.nih.gov/pubmed/37675102 http://dx.doi.org/10.3389/fimmu.2023.1258388 |
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