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AML classification in the year 2023: How to avoid a Babylonian confusion of languages

In parallel to the 5th edition of the World Health Organization Classification of Haematolymphoid Tumours (WHO 2022), an alternative International Consensus Classification (ICC) has been proposed. To evaluate the impact of the new classifications on AML diagnoses and ELN-based risk classification, w...

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Autores principales: Huber, Sandra, Baer, Constance, Hutter, Stephan, Dicker, Frank, Meggendorfer, Manja, Pohlkamp, Christian, Kern, Wolfgang, Haferlach, Torsten, Haferlach, Claudia, Hoermann, Gregor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317829/
https://www.ncbi.nlm.nih.gov/pubmed/37120689
http://dx.doi.org/10.1038/s41375-023-01909-w
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author Huber, Sandra
Baer, Constance
Hutter, Stephan
Dicker, Frank
Meggendorfer, Manja
Pohlkamp, Christian
Kern, Wolfgang
Haferlach, Torsten
Haferlach, Claudia
Hoermann, Gregor
author_facet Huber, Sandra
Baer, Constance
Hutter, Stephan
Dicker, Frank
Meggendorfer, Manja
Pohlkamp, Christian
Kern, Wolfgang
Haferlach, Torsten
Haferlach, Claudia
Hoermann, Gregor
author_sort Huber, Sandra
collection PubMed
description In parallel to the 5th edition of the World Health Organization Classification of Haematolymphoid Tumours (WHO 2022), an alternative International Consensus Classification (ICC) has been proposed. To evaluate the impact of the new classifications on AML diagnoses and ELN-based risk classification, we analyzed 717 MDS and 734 AML non-therapy-related patients diagnosed according to the revised 4th WHO edition (WHO 2017) by whole genome and transcriptome sequencing. In both new classifications, the purely morphologically defined AML entities decreased from 13% to 5%. Myelodysplasia-related (MR) AML increased from 22% to 28% (WHO 2022) and 26% (ICC). Other genetically-defined AML remained the largest group, and the abandoned AML-RUNX1 was mainly reclassified as AML-MR (WHO 2022: 77%; ICC: 96%). Different inclusion criteria of AML-CEBPA and AML-MR (i.a. exclusion of TP53 mutated cases according to ICC) were associated with differences in overall survival. In conclusion, both classifications focus on more genetics-based definitions with similar basic concepts and a large degree of agreement. The remaining non-comparability (e.g., TP53 mutated AML) needs additional studies to definitely answer open questions on disease categorization in an unbiased way.
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spelling pubmed-103178292023-07-05 AML classification in the year 2023: How to avoid a Babylonian confusion of languages Huber, Sandra Baer, Constance Hutter, Stephan Dicker, Frank Meggendorfer, Manja Pohlkamp, Christian Kern, Wolfgang Haferlach, Torsten Haferlach, Claudia Hoermann, Gregor Leukemia Article In parallel to the 5th edition of the World Health Organization Classification of Haematolymphoid Tumours (WHO 2022), an alternative International Consensus Classification (ICC) has been proposed. To evaluate the impact of the new classifications on AML diagnoses and ELN-based risk classification, we analyzed 717 MDS and 734 AML non-therapy-related patients diagnosed according to the revised 4th WHO edition (WHO 2017) by whole genome and transcriptome sequencing. In both new classifications, the purely morphologically defined AML entities decreased from 13% to 5%. Myelodysplasia-related (MR) AML increased from 22% to 28% (WHO 2022) and 26% (ICC). Other genetically-defined AML remained the largest group, and the abandoned AML-RUNX1 was mainly reclassified as AML-MR (WHO 2022: 77%; ICC: 96%). Different inclusion criteria of AML-CEBPA and AML-MR (i.a. exclusion of TP53 mutated cases according to ICC) were associated with differences in overall survival. In conclusion, both classifications focus on more genetics-based definitions with similar basic concepts and a large degree of agreement. The remaining non-comparability (e.g., TP53 mutated AML) needs additional studies to definitely answer open questions on disease categorization in an unbiased way. Nature Publishing Group UK 2023-04-29 2023 /pmc/articles/PMC10317829/ /pubmed/37120689 http://dx.doi.org/10.1038/s41375-023-01909-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huber, Sandra
Baer, Constance
Hutter, Stephan
Dicker, Frank
Meggendorfer, Manja
Pohlkamp, Christian
Kern, Wolfgang
Haferlach, Torsten
Haferlach, Claudia
Hoermann, Gregor
AML classification in the year 2023: How to avoid a Babylonian confusion of languages
title AML classification in the year 2023: How to avoid a Babylonian confusion of languages
title_full AML classification in the year 2023: How to avoid a Babylonian confusion of languages
title_fullStr AML classification in the year 2023: How to avoid a Babylonian confusion of languages
title_full_unstemmed AML classification in the year 2023: How to avoid a Babylonian confusion of languages
title_short AML classification in the year 2023: How to avoid a Babylonian confusion of languages
title_sort aml classification in the year 2023: how to avoid a babylonian confusion of languages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317829/
https://www.ncbi.nlm.nih.gov/pubmed/37120689
http://dx.doi.org/10.1038/s41375-023-01909-w
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