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Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor

Purpose: To present a case of a chemotherapy regimen combining a fibroblast growth factor receptor (FGFR) and mitogen-activated protein kinase kinase (MEK) inhibitor leading to serous retinopathy. Methods: A retrospective chart review of a single case was performed. Results: A 67-year-old man with p...

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Autores principales: Day, H. Russell, Finn, Avni P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621699/
https://www.ncbi.nlm.nih.gov/pubmed/37927314
http://dx.doi.org/10.1177/24741264231163393
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author Day, H. Russell
Finn, Avni P.
author_facet Day, H. Russell
Finn, Avni P.
author_sort Day, H. Russell
collection PubMed
description Purpose: To present a case of a chemotherapy regimen combining a fibroblast growth factor receptor (FGFR) and mitogen-activated protein kinase kinase (MEK) inhibitor leading to serous retinopathy. Methods: A retrospective chart review of a single case was performed. Results: A 67-year-old man with pancreatic and prostate cancer developed bilateral multifocal pockets of subretinal fluid while on an experimental chemotherapy regimen combining an MEK inhibitor (trametinib) and an FGFR inhibitor (erdafitinib). Conclusions: Given that FGFR lies upstream to the mitogen-activated protein kinase signaling pathway, retinal toxicity may be more severe and more common with FGFR–MEK combination therapy. Future studies are necessary to guide ophthalmic surveillance.
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spelling pubmed-106216992023-11-03 Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor Day, H. Russell Finn, Avni P. J Vitreoretin Dis Case Reports Purpose: To present a case of a chemotherapy regimen combining a fibroblast growth factor receptor (FGFR) and mitogen-activated protein kinase kinase (MEK) inhibitor leading to serous retinopathy. Methods: A retrospective chart review of a single case was performed. Results: A 67-year-old man with pancreatic and prostate cancer developed bilateral multifocal pockets of subretinal fluid while on an experimental chemotherapy regimen combining an MEK inhibitor (trametinib) and an FGFR inhibitor (erdafitinib). Conclusions: Given that FGFR lies upstream to the mitogen-activated protein kinase signaling pathway, retinal toxicity may be more severe and more common with FGFR–MEK combination therapy. Future studies are necessary to guide ophthalmic surveillance. SAGE Publications 2023-04-10 /pmc/articles/PMC10621699/ /pubmed/37927314 http://dx.doi.org/10.1177/24741264231163393 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Reports
Day, H. Russell
Finn, Avni P.
Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor
title Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor
title_full Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor
title_fullStr Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor
title_full_unstemmed Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor
title_short Serous Retinopathy Associated With Combination MEK and Fibroblast Growth Factor Receptor Inhibitor
title_sort serous retinopathy associated with combination mek and fibroblast growth factor receptor inhibitor
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621699/
https://www.ncbi.nlm.nih.gov/pubmed/37927314
http://dx.doi.org/10.1177/24741264231163393
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