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Novel Therapies for Aggressive B-Cell Lymphoma

Aggressive B-cell lymphoma (BCL) comprises a heterogeneous group of malignancies, including diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma, and mantle cell lymphoma (MCL). DLBCL, with its 3 subtypes, is the most common type of lymphoma. Advances in chemoimmunotherapy have substantially impr...

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Detalles Bibliográficos
Autores principales: Foon, Kenneth A., Takeshita, Kenichi, Zinzani, Pier L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318210/
https://www.ncbi.nlm.nih.gov/pubmed/22536253
http://dx.doi.org/10.1155/2012/302570
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author Foon, Kenneth A.
Takeshita, Kenichi
Zinzani, Pier L.
author_facet Foon, Kenneth A.
Takeshita, Kenichi
Zinzani, Pier L.
author_sort Foon, Kenneth A.
collection PubMed
description Aggressive B-cell lymphoma (BCL) comprises a heterogeneous group of malignancies, including diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma, and mantle cell lymphoma (MCL). DLBCL, with its 3 subtypes, is the most common type of lymphoma. Advances in chemoimmunotherapy have substantially improved disease control. However, depending on the subtype, patients with DLBCL still exhibit substantially different survival rates. In MCL, a mature B-cell lymphoma, the addition of rituximab to conventional chemotherapy regimens has increased response rates, but not survival. Burkitt lymphoma, the most aggressive BCL, is characterized by a high proliferative index and requires more intensive chemotherapy regimens than DLBCL. Hence, there is a need for more effective therapies for all three diseases. Increased understanding of the molecular features of aggressive BCL has led to the development of a range of novel therapies, many of which target the tumor in a tailored manner and are summarized in this paper.
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spelling pubmed-33182102012-04-25 Novel Therapies for Aggressive B-Cell Lymphoma Foon, Kenneth A. Takeshita, Kenichi Zinzani, Pier L. Adv Hematol Review Article Aggressive B-cell lymphoma (BCL) comprises a heterogeneous group of malignancies, including diffuse large B-cell lymphoma (DLBCL), Burkitt lymphoma, and mantle cell lymphoma (MCL). DLBCL, with its 3 subtypes, is the most common type of lymphoma. Advances in chemoimmunotherapy have substantially improved disease control. However, depending on the subtype, patients with DLBCL still exhibit substantially different survival rates. In MCL, a mature B-cell lymphoma, the addition of rituximab to conventional chemotherapy regimens has increased response rates, but not survival. Burkitt lymphoma, the most aggressive BCL, is characterized by a high proliferative index and requires more intensive chemotherapy regimens than DLBCL. Hence, there is a need for more effective therapies for all three diseases. Increased understanding of the molecular features of aggressive BCL has led to the development of a range of novel therapies, many of which target the tumor in a tailored manner and are summarized in this paper. Hindawi Publishing Corporation 2012 2012-03-25 /pmc/articles/PMC3318210/ /pubmed/22536253 http://dx.doi.org/10.1155/2012/302570 Text en Copyright © 2012 Kenneth A. Foon et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Foon, Kenneth A.
Takeshita, Kenichi
Zinzani, Pier L.
Novel Therapies for Aggressive B-Cell Lymphoma
title Novel Therapies for Aggressive B-Cell Lymphoma
title_full Novel Therapies for Aggressive B-Cell Lymphoma
title_fullStr Novel Therapies for Aggressive B-Cell Lymphoma
title_full_unstemmed Novel Therapies for Aggressive B-Cell Lymphoma
title_short Novel Therapies for Aggressive B-Cell Lymphoma
title_sort novel therapies for aggressive b-cell lymphoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3318210/
https://www.ncbi.nlm.nih.gov/pubmed/22536253
http://dx.doi.org/10.1155/2012/302570
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