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Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma
PURPOSE OF REVIEW: Rituximab-based chemoimmunotherapy has resulted in a marked improvement in the survival of diffuse large B cell lymphoma (DLBCL). We reflect upon the history front-line (1L) therapy and highlight advances in management. RECENT FINDINGS: Since the introduction of R-CHOP, the majori...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647877/ https://www.ncbi.nlm.nih.gov/pubmed/31254155 http://dx.doi.org/10.1007/s11899-019-00518-8 |
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author | Kesavan, Murali Eyre, Toby A. Collins, Graham P. |
author_facet | Kesavan, Murali Eyre, Toby A. Collins, Graham P. |
author_sort | Kesavan, Murali |
collection | PubMed |
description | PURPOSE OF REVIEW: Rituximab-based chemoimmunotherapy has resulted in a marked improvement in the survival of diffuse large B cell lymphoma (DLBCL). We reflect upon the history front-line (1L) therapy and highlight advances in management. RECENT FINDINGS: Since the introduction of R-CHOP, the majority of randomized studies in the front-line treatment of DLBCL have failed to show a benefit. Such studies have involved treatment intensification, adding novel agents to the R-CHOP backbone and targeting such novel agents to biologically defined subgroups. R-CHOP therefore remains standard-of-care for most but new insights into the molecular biology of these diseases, and the development of active targeted molecules offers promise for the future. Accumulating evidence in the very elderly suggests dose attenuation does not compromise survival. Intensification in primary mediastinal B cell lymphoma may avoid the need for radiotherapy, but must be balanced against the risks. PET-CT- and ctDNA-based response assessment may now enable response adapted therapy and early prognostication, improving patient selection and potentially outcomes. SUMMARY: Novel technologies and therapies in combination with novel molecular diagnostics will likely become the standard-of-care approach for the personalized therapy of DLBCL but need to be proven in well-designed and conducted randomized trials. |
format | Online Article Text |
id | pubmed-6647877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-66478772019-08-09 Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma Kesavan, Murali Eyre, Toby A. Collins, Graham P. Curr Hematol Malig Rep B-cell NHL, T-cell NHL, and Hodgkin Lymphoma (J Amengual, Section Editor) PURPOSE OF REVIEW: Rituximab-based chemoimmunotherapy has resulted in a marked improvement in the survival of diffuse large B cell lymphoma (DLBCL). We reflect upon the history front-line (1L) therapy and highlight advances in management. RECENT FINDINGS: Since the introduction of R-CHOP, the majority of randomized studies in the front-line treatment of DLBCL have failed to show a benefit. Such studies have involved treatment intensification, adding novel agents to the R-CHOP backbone and targeting such novel agents to biologically defined subgroups. R-CHOP therefore remains standard-of-care for most but new insights into the molecular biology of these diseases, and the development of active targeted molecules offers promise for the future. Accumulating evidence in the very elderly suggests dose attenuation does not compromise survival. Intensification in primary mediastinal B cell lymphoma may avoid the need for radiotherapy, but must be balanced against the risks. PET-CT- and ctDNA-based response assessment may now enable response adapted therapy and early prognostication, improving patient selection and potentially outcomes. SUMMARY: Novel technologies and therapies in combination with novel molecular diagnostics will likely become the standard-of-care approach for the personalized therapy of DLBCL but need to be proven in well-designed and conducted randomized trials. Springer US 2019-06-29 2019 /pmc/articles/PMC6647877/ /pubmed/31254155 http://dx.doi.org/10.1007/s11899-019-00518-8 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | B-cell NHL, T-cell NHL, and Hodgkin Lymphoma (J Amengual, Section Editor) Kesavan, Murali Eyre, Toby A. Collins, Graham P. Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma |
title | Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma |
title_full | Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma |
title_fullStr | Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma |
title_full_unstemmed | Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma |
title_short | Front-Line Treatment of High Grade B Cell Non-Hodgkin Lymphoma |
title_sort | front-line treatment of high grade b cell non-hodgkin lymphoma |
topic | B-cell NHL, T-cell NHL, and Hodgkin Lymphoma (J Amengual, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647877/ https://www.ncbi.nlm.nih.gov/pubmed/31254155 http://dx.doi.org/10.1007/s11899-019-00518-8 |
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