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Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma

With the increasing use of next-generation sequencing, highly effective targeted therapies have been emerging as treatment options for several cancer types. Recurrent gene-fusions have been recognized in sarcomas; however, options for targeted therapy remain scarce. Here, we describe a case of a sar...

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Autores principales: Schrenk, Karin G., Weschenfelder, Wolfram, Spiegel, Christian, Agaimy, Abbas, Stöhr, Robert, Hartmann, Arndt, Gaßler, Nikolaus, Drescher, Robert, Freesmeyer, Martin, Malouhi, Amer, Bürckenmeyer, Florian, Aschenbach, René, Teichgräber, Ulf, Kögler, Christine, Vogt, Matthias, Hofmann, Gunther O., Hochhaus, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356868/
https://www.ncbi.nlm.nih.gov/pubmed/36469155
http://dx.doi.org/10.1007/s00432-022-04496-y
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author Schrenk, Karin G.
Weschenfelder, Wolfram
Spiegel, Christian
Agaimy, Abbas
Stöhr, Robert
Hartmann, Arndt
Gaßler, Nikolaus
Drescher, Robert
Freesmeyer, Martin
Malouhi, Amer
Bürckenmeyer, Florian
Aschenbach, René
Teichgräber, Ulf
Kögler, Christine
Vogt, Matthias
Hofmann, Gunther O.
Hochhaus, Andreas
author_facet Schrenk, Karin G.
Weschenfelder, Wolfram
Spiegel, Christian
Agaimy, Abbas
Stöhr, Robert
Hartmann, Arndt
Gaßler, Nikolaus
Drescher, Robert
Freesmeyer, Martin
Malouhi, Amer
Bürckenmeyer, Florian
Aschenbach, René
Teichgräber, Ulf
Kögler, Christine
Vogt, Matthias
Hofmann, Gunther O.
Hochhaus, Andreas
author_sort Schrenk, Karin G.
collection PubMed
description With the increasing use of next-generation sequencing, highly effective targeted therapies have been emerging as treatment options for several cancer types. Recurrent gene-fusions have been recognized in sarcomas; however, options for targeted therapy remain scarce. Here, we describe a case of a sarcoma, associated with a RET::TRIM33-fusion gene with an exceptional response to a neoadjuvant therapy with the selective RET inhibitor selpercatinib. Resected tumor revealed subtotal histopathologic response. This is the first report of successful targeted therapy with selpercatinib in RET-fusion-associated sarcomas. As new targeted therapies are under development, similar treatment options may become available for sarcoma patients.
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spelling pubmed-103568682023-07-21 Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma Schrenk, Karin G. Weschenfelder, Wolfram Spiegel, Christian Agaimy, Abbas Stöhr, Robert Hartmann, Arndt Gaßler, Nikolaus Drescher, Robert Freesmeyer, Martin Malouhi, Amer Bürckenmeyer, Florian Aschenbach, René Teichgräber, Ulf Kögler, Christine Vogt, Matthias Hofmann, Gunther O. Hochhaus, Andreas J Cancer Res Clin Oncol Research With the increasing use of next-generation sequencing, highly effective targeted therapies have been emerging as treatment options for several cancer types. Recurrent gene-fusions have been recognized in sarcomas; however, options for targeted therapy remain scarce. Here, we describe a case of a sarcoma, associated with a RET::TRIM33-fusion gene with an exceptional response to a neoadjuvant therapy with the selective RET inhibitor selpercatinib. Resected tumor revealed subtotal histopathologic response. This is the first report of successful targeted therapy with selpercatinib in RET-fusion-associated sarcomas. As new targeted therapies are under development, similar treatment options may become available for sarcoma patients. Springer Berlin Heidelberg 2022-12-05 2023 /pmc/articles/PMC10356868/ /pubmed/36469155 http://dx.doi.org/10.1007/s00432-022-04496-y Text en © The Author(s) 2022 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/) .
spellingShingle Research
Schrenk, Karin G.
Weschenfelder, Wolfram
Spiegel, Christian
Agaimy, Abbas
Stöhr, Robert
Hartmann, Arndt
Gaßler, Nikolaus
Drescher, Robert
Freesmeyer, Martin
Malouhi, Amer
Bürckenmeyer, Florian
Aschenbach, René
Teichgräber, Ulf
Kögler, Christine
Vogt, Matthias
Hofmann, Gunther O.
Hochhaus, Andreas
Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma
title Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma
title_full Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma
title_fullStr Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma
title_full_unstemmed Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma
title_short Exceptional response to neoadjuvant targeted therapy with the selective RET inhibitor selpercatinib in RET-fusion-associated sarcoma
title_sort exceptional response to neoadjuvant targeted therapy with the selective ret inhibitor selpercatinib in ret-fusion-associated sarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356868/
https://www.ncbi.nlm.nih.gov/pubmed/36469155
http://dx.doi.org/10.1007/s00432-022-04496-y
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