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Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience

BACKGROUND: Sarcomas are a heterogeneous group of rare malignant tumors with more than 100 subtypes. Accurate diagnosis remains challenging due to a lack of characteristic molecular or histomorphological hallmarks. A DNA methylation-based tumor profiling classifier for sarcomas (known as sarcoma cla...

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Autores principales: Roohani, Siyer, Ehret, Felix, Perez, Eilís, Capper, David, Jarosch, Armin, Flörcken, Anne, Märdian, Sven, Zips, Daniel, Kaul, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667620/
https://www.ncbi.nlm.nih.gov/pubmed/36380356
http://dx.doi.org/10.1186/s13148-022-01365-w
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author Roohani, Siyer
Ehret, Felix
Perez, Eilís
Capper, David
Jarosch, Armin
Flörcken, Anne
Märdian, Sven
Zips, Daniel
Kaul, David
author_facet Roohani, Siyer
Ehret, Felix
Perez, Eilís
Capper, David
Jarosch, Armin
Flörcken, Anne
Märdian, Sven
Zips, Daniel
Kaul, David
author_sort Roohani, Siyer
collection PubMed
description BACKGROUND: Sarcomas are a heterogeneous group of rare malignant tumors with more than 100 subtypes. Accurate diagnosis remains challenging due to a lack of characteristic molecular or histomorphological hallmarks. A DNA methylation-based tumor profiling classifier for sarcomas (known as sarcoma classifier) from the German Cancer Research Center (Deutsches Krebsforschungszentrum) is now employed in selected cases to guide tumor classification and treatment decisions at our institution. Data on the usage of the classifier in daily clinical routine are lacking. METHODS: In this single-center experience, we describe the clinical course of five sarcoma cases undergoing thorough pathological and reference pathological examination as well as DNA methylation-based profiling and their impact on subsequent treatment decisions. We collected data on the clinical course, DNA methylation analysis, histopathology, radiological imaging, and next-generation sequencing. RESULTS: Five clinical cases involving DNA methylation-based profiling in 2021 at our institution were included. All patients’ DNA methylation profiles were successfully matched to a methylation profile cluster of the sarcoma classifier’s dataset. In three patients, the classifier reassured diagnosis or aided in finding the correct diagnosis in light of contradictory data and differential diagnoses. In two patients with intracranial tumors, the classifier changed the diagnosis to a novel diagnostic tumor group. CONCLUSIONS: The sarcoma classifier is a valuable diagnostic tool that should be used after comprehensive clinical and histopathological evaluation. It may help to reassure the histopathological diagnosis or indicate the need for thorough reassessment in cases where it contradicts previous findings. However, certain limitations (non-classifiable cases, misclassifications, unclear degree of sample purity for analysis and others) currently preclude wide clinical application. The current sarcoma classifier is therefore not yet ready for a broad clinical routine. With further refinements, this promising tool may be implemented in daily clinical practice in selected cases.
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spelling pubmed-96676202022-11-17 Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience Roohani, Siyer Ehret, Felix Perez, Eilís Capper, David Jarosch, Armin Flörcken, Anne Märdian, Sven Zips, Daniel Kaul, David Clin Epigenetics Research BACKGROUND: Sarcomas are a heterogeneous group of rare malignant tumors with more than 100 subtypes. Accurate diagnosis remains challenging due to a lack of characteristic molecular or histomorphological hallmarks. A DNA methylation-based tumor profiling classifier for sarcomas (known as sarcoma classifier) from the German Cancer Research Center (Deutsches Krebsforschungszentrum) is now employed in selected cases to guide tumor classification and treatment decisions at our institution. Data on the usage of the classifier in daily clinical routine are lacking. METHODS: In this single-center experience, we describe the clinical course of five sarcoma cases undergoing thorough pathological and reference pathological examination as well as DNA methylation-based profiling and their impact on subsequent treatment decisions. We collected data on the clinical course, DNA methylation analysis, histopathology, radiological imaging, and next-generation sequencing. RESULTS: Five clinical cases involving DNA methylation-based profiling in 2021 at our institution were included. All patients’ DNA methylation profiles were successfully matched to a methylation profile cluster of the sarcoma classifier’s dataset. In three patients, the classifier reassured diagnosis or aided in finding the correct diagnosis in light of contradictory data and differential diagnoses. In two patients with intracranial tumors, the classifier changed the diagnosis to a novel diagnostic tumor group. CONCLUSIONS: The sarcoma classifier is a valuable diagnostic tool that should be used after comprehensive clinical and histopathological evaluation. It may help to reassure the histopathological diagnosis or indicate the need for thorough reassessment in cases where it contradicts previous findings. However, certain limitations (non-classifiable cases, misclassifications, unclear degree of sample purity for analysis and others) currently preclude wide clinical application. The current sarcoma classifier is therefore not yet ready for a broad clinical routine. With further refinements, this promising tool may be implemented in daily clinical practice in selected cases. BioMed Central 2022-11-15 /pmc/articles/PMC9667620/ /pubmed/36380356 http://dx.doi.org/10.1186/s13148-022-01365-w 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Roohani, Siyer
Ehret, Felix
Perez, Eilís
Capper, David
Jarosch, Armin
Flörcken, Anne
Märdian, Sven
Zips, Daniel
Kaul, David
Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience
title Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience
title_full Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience
title_fullStr Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience
title_full_unstemmed Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience
title_short Sarcoma classification by DNA methylation profiling in clinical everyday life: the Charité experience
title_sort sarcoma classification by dna methylation profiling in clinical everyday life: the charité experience
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667620/
https://www.ncbi.nlm.nih.gov/pubmed/36380356
http://dx.doi.org/10.1186/s13148-022-01365-w
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