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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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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. |
format | Online Article Text |
id | pubmed-10356868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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