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Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge

Diffuse Large B Cell lymphoma (DLBCL) is the commonest non-Hodgkin lymphoma. Over the last two decades tremendous progress has been made in our understanding of the molecular pathogenesis of DLBCL. However, this biological understanding has not yet been translated into improved first-line therapy. A...

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Autores principales: Cutmore, Natasha H., Krupka, Joanna A., Hodson, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614242/
https://www.ncbi.nlm.nih.gov/pubmed/36788062
http://dx.doi.org/10.1016/j.modpat.2022.100007
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author Cutmore, Natasha H.
Krupka, Joanna A.
Hodson, Daniel J.
author_facet Cutmore, Natasha H.
Krupka, Joanna A.
Hodson, Daniel J.
author_sort Cutmore, Natasha H.
collection PubMed
description Diffuse Large B Cell lymphoma (DLBCL) is the commonest non-Hodgkin lymphoma. Over the last two decades tremendous progress has been made in our understanding of the molecular pathogenesis of DLBCL. However, this biological understanding has not yet been translated into improved first-line therapy. A major barrier to the introduction of molecularly targeted therapy in DLBCL is the considerable molecular heterogeneity of this disease. Recent studies have tried to rationalise this heterogeneity by proposing new genetic subtypes of DLBCL. Whilst remarkable consensus exists over the broad nature of these genetic subtypes, important questions remain over precisely how, or even why, genetic subtyping might be incorporated into diagnostic laboratories. In this review we compare the findings of the major genetic subtyping studies and discuss the implications this may have for diagnostic pathology services and the management of DLBCL.
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spelling pubmed-76142422023-02-25 Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge Cutmore, Natasha H. Krupka, Joanna A. Hodson, Daniel J. Mod Pathol Article Diffuse Large B Cell lymphoma (DLBCL) is the commonest non-Hodgkin lymphoma. Over the last two decades tremendous progress has been made in our understanding of the molecular pathogenesis of DLBCL. However, this biological understanding has not yet been translated into improved first-line therapy. A major barrier to the introduction of molecularly targeted therapy in DLBCL is the considerable molecular heterogeneity of this disease. Recent studies have tried to rationalise this heterogeneity by proposing new genetic subtypes of DLBCL. Whilst remarkable consensus exists over the broad nature of these genetic subtypes, important questions remain over precisely how, or even why, genetic subtyping might be incorporated into diagnostic laboratories. In this review we compare the findings of the major genetic subtyping studies and discuss the implications this may have for diagnostic pathology services and the management of DLBCL. 2023-01-01 /pmc/articles/PMC7614242/ /pubmed/36788062 http://dx.doi.org/10.1016/j.modpat.2022.100007 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license.
spellingShingle Article
Cutmore, Natasha H.
Krupka, Joanna A.
Hodson, Daniel J.
Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge
title Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge
title_full Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge
title_fullStr Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge
title_full_unstemmed Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge
title_short Genetic Profiling in Diffuse Large B Cell Lymphoma – the promise and the challenge
title_sort genetic profiling in diffuse large b cell lymphoma – the promise and the challenge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614242/
https://www.ncbi.nlm.nih.gov/pubmed/36788062
http://dx.doi.org/10.1016/j.modpat.2022.100007
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