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Genetic lesions and targeted therapy in Hodgkin lymphoma

Hodgkin lymphoma is a special type of lymphoma in which tumor cells frequently undergo multiple genetic lesions that are associated with accompanying pathway abnormalities. These pathway abnormalities are dominated by active signaling pathways, such as the JAK-STAT (Janus kinase–signal transducer an...

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Autores principales: Li, Zhe, Mu, Wei, Xiao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841868/
https://www.ncbi.nlm.nih.gov/pubmed/36654739
http://dx.doi.org/10.1177/20406207221149245
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author Li, Zhe
Mu, Wei
Xiao, Min
author_facet Li, Zhe
Mu, Wei
Xiao, Min
author_sort Li, Zhe
collection PubMed
description Hodgkin lymphoma is a special type of lymphoma in which tumor cells frequently undergo multiple genetic lesions that are associated with accompanying pathway abnormalities. These pathway abnormalities are dominated by active signaling pathways, such as the JAK-STAT (Janus kinase–signal transducer and activator of transcription) pathway and the NFκB (nuclear factor kappa-B) pathway, which usually result in hyperactive survival signaling. Targeted therapies often play an important role in hematologic malignancies, such as CAR-T therapy (chimeric antigen receptor T-cell immunotherapy) targeting CD19 and CD22 in diffuse large B-cell lymphoma, while in Hodgkin lymphoma, the main targets of targeted therapies are CD30 molecules and PD1 molecules. Drugs targeting other molecules are also under investigation. This review summarizes the actionable genetic lesions, current treatment options, clinical trials for Hodgkin lymphoma and the potential value of those genetic lesions in clinical applications.
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spelling pubmed-98418682023-01-17 Genetic lesions and targeted therapy in Hodgkin lymphoma Li, Zhe Mu, Wei Xiao, Min Ther Adv Hematol Review Hodgkin lymphoma is a special type of lymphoma in which tumor cells frequently undergo multiple genetic lesions that are associated with accompanying pathway abnormalities. These pathway abnormalities are dominated by active signaling pathways, such as the JAK-STAT (Janus kinase–signal transducer and activator of transcription) pathway and the NFκB (nuclear factor kappa-B) pathway, which usually result in hyperactive survival signaling. Targeted therapies often play an important role in hematologic malignancies, such as CAR-T therapy (chimeric antigen receptor T-cell immunotherapy) targeting CD19 and CD22 in diffuse large B-cell lymphoma, while in Hodgkin lymphoma, the main targets of targeted therapies are CD30 molecules and PD1 molecules. Drugs targeting other molecules are also under investigation. This review summarizes the actionable genetic lesions, current treatment options, clinical trials for Hodgkin lymphoma and the potential value of those genetic lesions in clinical applications. SAGE Publications 2023-01-12 /pmc/articles/PMC9841868/ /pubmed/36654739 http://dx.doi.org/10.1177/20406207221149245 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Li, Zhe
Mu, Wei
Xiao, Min
Genetic lesions and targeted therapy in Hodgkin lymphoma
title Genetic lesions and targeted therapy in Hodgkin lymphoma
title_full Genetic lesions and targeted therapy in Hodgkin lymphoma
title_fullStr Genetic lesions and targeted therapy in Hodgkin lymphoma
title_full_unstemmed Genetic lesions and targeted therapy in Hodgkin lymphoma
title_short Genetic lesions and targeted therapy in Hodgkin lymphoma
title_sort genetic lesions and targeted therapy in hodgkin lymphoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841868/
https://www.ncbi.nlm.nih.gov/pubmed/36654739
http://dx.doi.org/10.1177/20406207221149245
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