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International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms

The recently published International Consensus Classification (ICC) of myeloid neoplasms summarized the results of an in-depth effort by pathologists, oncologists, and geneticists aimed to update the 2017 World Health Organization classification system for hematopoietic tumors. Along these lines, se...

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Autores principales: Gianelli, Umberto, Thiele, Jürgen, Orazi, Attilio, Gangat, Naseema, Vannucchi, Alessandro M., Tefferi, Ayalew, Kvasnicka, Hans Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852206/
https://www.ncbi.nlm.nih.gov/pubmed/36580136
http://dx.doi.org/10.1007/s00428-022-03480-8
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author Gianelli, Umberto
Thiele, Jürgen
Orazi, Attilio
Gangat, Naseema
Vannucchi, Alessandro M.
Tefferi, Ayalew
Kvasnicka, Hans Michael
author_facet Gianelli, Umberto
Thiele, Jürgen
Orazi, Attilio
Gangat, Naseema
Vannucchi, Alessandro M.
Tefferi, Ayalew
Kvasnicka, Hans Michael
author_sort Gianelli, Umberto
collection PubMed
description The recently published International Consensus Classification (ICC) of myeloid neoplasms summarized the results of an in-depth effort by pathologists, oncologists, and geneticists aimed to update the 2017 World Health Organization classification system for hematopoietic tumors. Along these lines, several important modifications were implemented in the classification of myeloproliferative neoplasms (MPNs). For chronic myeloid leukemia, BCR::ABL1-positive, the definition of accelerated and blast phase was simplified, and in the BCR::ABL1-negative MPNs, the classification was slightly updated to improve diagnostic specificity with a more detailed and better validated morphologic approach and the recommendation of more sensitive molecular techniques to capture in particular early stage diseases. In this regard, high sensitive single target (RT-qPCR, ddPCR) or multi-target next-generation sequencing assays with a minimal sensitivity of VAF 1% are now important for a proper diagnostic identification of MPN cases with low allelic frequencies at initial presentation. This review discusses the updated diagnostic criteria of MPN according to the ICC, particularly by highlighting the new concepts and how they can be applied in clinical settings to obtain an appropriate prognostic relevant diagnosis.
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spelling pubmed-98522062023-01-21 International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms Gianelli, Umberto Thiele, Jürgen Orazi, Attilio Gangat, Naseema Vannucchi, Alessandro M. Tefferi, Ayalew Kvasnicka, Hans Michael Virchows Arch Review The recently published International Consensus Classification (ICC) of myeloid neoplasms summarized the results of an in-depth effort by pathologists, oncologists, and geneticists aimed to update the 2017 World Health Organization classification system for hematopoietic tumors. Along these lines, several important modifications were implemented in the classification of myeloproliferative neoplasms (MPNs). For chronic myeloid leukemia, BCR::ABL1-positive, the definition of accelerated and blast phase was simplified, and in the BCR::ABL1-negative MPNs, the classification was slightly updated to improve diagnostic specificity with a more detailed and better validated morphologic approach and the recommendation of more sensitive molecular techniques to capture in particular early stage diseases. In this regard, high sensitive single target (RT-qPCR, ddPCR) or multi-target next-generation sequencing assays with a minimal sensitivity of VAF 1% are now important for a proper diagnostic identification of MPN cases with low allelic frequencies at initial presentation. This review discusses the updated diagnostic criteria of MPN according to the ICC, particularly by highlighting the new concepts and how they can be applied in clinical settings to obtain an appropriate prognostic relevant diagnosis. Springer Berlin Heidelberg 2022-12-29 2023 /pmc/articles/PMC9852206/ /pubmed/36580136 http://dx.doi.org/10.1007/s00428-022-03480-8 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 Review
Gianelli, Umberto
Thiele, Jürgen
Orazi, Attilio
Gangat, Naseema
Vannucchi, Alessandro M.
Tefferi, Ayalew
Kvasnicka, Hans Michael
International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
title International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
title_full International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
title_fullStr International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
title_full_unstemmed International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
title_short International Consensus Classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
title_sort international consensus classification of myeloid and lymphoid neoplasms: myeloproliferative neoplasms
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852206/
https://www.ncbi.nlm.nih.gov/pubmed/36580136
http://dx.doi.org/10.1007/s00428-022-03480-8
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