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Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax

B cell prolymphocytic leukemia is a rare and aggressive disorder often with high risk features including TP53 mutation, deletion 17p and complex karyotype. There is scarcity of data regarding treatment and existing therapies induce short lived remissions. Ibrutinib, a Bruton tyrosine kinase inhibito...

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Detalles Bibliográficos
Autores principales: Siddiqui, Maria Tariq, Price, Allyson, Ferrajoli, Alessandra, Borthakur, Gautam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515291/
https://www.ncbi.nlm.nih.gov/pubmed/34692401
http://dx.doi.org/10.1016/j.lrr.2021.100266
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author Siddiqui, Maria Tariq
Price, Allyson
Ferrajoli, Alessandra
Borthakur, Gautam
author_facet Siddiqui, Maria Tariq
Price, Allyson
Ferrajoli, Alessandra
Borthakur, Gautam
author_sort Siddiqui, Maria Tariq
collection PubMed
description B cell prolymphocytic leukemia is a rare and aggressive disorder often with high risk features including TP53 mutation, deletion 17p and complex karyotype. There is scarcity of data regarding treatment and existing therapies induce short lived remissions. Ibrutinib, a Bruton tyrosine kinase inhibitor, has had success in some patients with high risk features. Venetoclax, a BCL-2 inhibitor, has primarily been used in the relapsed setting. We present a case of B PLL with deletion 17p and mutated TP53 treated with ibrutinib and venetoclax in the frontline setting which resulted in measurable/minimal residual disease negative remission for approximately three years.
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spelling pubmed-85152912021-10-21 Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax Siddiqui, Maria Tariq Price, Allyson Ferrajoli, Alessandra Borthakur, Gautam Leuk Res Rep Article B cell prolymphocytic leukemia is a rare and aggressive disorder often with high risk features including TP53 mutation, deletion 17p and complex karyotype. There is scarcity of data regarding treatment and existing therapies induce short lived remissions. Ibrutinib, a Bruton tyrosine kinase inhibitor, has had success in some patients with high risk features. Venetoclax, a BCL-2 inhibitor, has primarily been used in the relapsed setting. We present a case of B PLL with deletion 17p and mutated TP53 treated with ibrutinib and venetoclax in the frontline setting which resulted in measurable/minimal residual disease negative remission for approximately three years. Elsevier 2021-08-30 /pmc/articles/PMC8515291/ /pubmed/34692401 http://dx.doi.org/10.1016/j.lrr.2021.100266 Text en © 2021 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Siddiqui, Maria Tariq
Price, Allyson
Ferrajoli, Alessandra
Borthakur, Gautam
Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax
title Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax
title_full Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax
title_fullStr Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax
title_full_unstemmed Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax
title_short Sustained MRD negative remission in del17p and TP53 mutated B cell prolymphocytic leukemia with ibrutinib and venetoclax
title_sort sustained mrd negative remission in del17p and tp53 mutated b cell prolymphocytic leukemia with ibrutinib and venetoclax
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515291/
https://www.ncbi.nlm.nih.gov/pubmed/34692401
http://dx.doi.org/10.1016/j.lrr.2021.100266
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