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Current trends in the management of Richter's syndrome

Richter's syndrome (RS) is a life-threatening complication of chronic lymphocytic leukemia (CLL). While previous research has increased our knowledge on the distinct evolutionary patterns of RS and provided a deeper understanding of the risk factors and molecular events predisposing to transfor...

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Autores principales: Allan, John N, Furman, Richard R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331753/
https://www.ncbi.nlm.nih.gov/pubmed/30651968
http://dx.doi.org/10.2217/ijh-2018-0010
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author Allan, John N
Furman, Richard R
author_facet Allan, John N
Furman, Richard R
author_sort Allan, John N
collection PubMed
description Richter's syndrome (RS) is a life-threatening complication of chronic lymphocytic leukemia (CLL). While previous research has increased our knowledge on the distinct evolutionary patterns of RS and provided a deeper understanding of the risk factors and molecular events predisposing to transformation, there remain few targetable aberrations and treatment is largely ineffective. The ability to obtain deeper remissions, without selecting for deletion 17p, by using novel B-cell receptor (BCR) antagonists and bcl2 inhibition might lead to a decrease in the incidence of RS, but these agents have done little to significantly change outcomes when incorporated into treatment regimens for RS. In this review we highlight the current landscape of molecular lesions specific to RS, review the data on historical treatment options, and look to the horizon for potential opportunities in the future.
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spelling pubmed-63317532019-01-16 Current trends in the management of Richter's syndrome Allan, John N Furman, Richard R Int J Hematol Oncol Review Richter's syndrome (RS) is a life-threatening complication of chronic lymphocytic leukemia (CLL). While previous research has increased our knowledge on the distinct evolutionary patterns of RS and provided a deeper understanding of the risk factors and molecular events predisposing to transformation, there remain few targetable aberrations and treatment is largely ineffective. The ability to obtain deeper remissions, without selecting for deletion 17p, by using novel B-cell receptor (BCR) antagonists and bcl2 inhibition might lead to a decrease in the incidence of RS, but these agents have done little to significantly change outcomes when incorporated into treatment regimens for RS. In this review we highlight the current landscape of molecular lesions specific to RS, review the data on historical treatment options, and look to the horizon for potential opportunities in the future. Future Medicine Ltd 2019-01-08 /pmc/articles/PMC6331753/ /pubmed/30651968 http://dx.doi.org/10.2217/ijh-2018-0010 Text en © 2018 John N Allen This work is licensed under a Creative Commons Attribution-NonCommercial NonDerivative 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
Allan, John N
Furman, Richard R
Current trends in the management of Richter's syndrome
title Current trends in the management of Richter's syndrome
title_full Current trends in the management of Richter's syndrome
title_fullStr Current trends in the management of Richter's syndrome
title_full_unstemmed Current trends in the management of Richter's syndrome
title_short Current trends in the management of Richter's syndrome
title_sort current trends in the management of richter's syndrome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331753/
https://www.ncbi.nlm.nih.gov/pubmed/30651968
http://dx.doi.org/10.2217/ijh-2018-0010
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