Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kesavan, Murali, Eyre, Toby A., Collins, Graham P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
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
_version_ 1783437762708373504
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
work_keys_str_mv AT kesavanmurali frontlinetreatmentofhighgradebcellnonhodgkinlymphoma
AT eyretobya frontlinetreatmentofhighgradebcellnonhodgkinlymphoma
AT collinsgrahamp frontlinetreatmentofhighgradebcellnonhodgkinlymphoma