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PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma

Recent results of randomized phase III studies of FDG-PET-adapted therapy for advanced Hodgkin lymphoma (HL) have clearly demonstrated benefit to alteration of treatment according to interim response, in particular regarding reducing toxicity while maintaining efficacy. However, these studies have d...

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Detalles Bibliográficos
Autores principales: Lang, Noemie, Crump, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268111/
https://www.ncbi.nlm.nih.gov/pubmed/32537115
http://dx.doi.org/10.1177/2040620720914490
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author Lang, Noemie
Crump, Michael
author_facet Lang, Noemie
Crump, Michael
author_sort Lang, Noemie
collection PubMed
description Recent results of randomized phase III studies of FDG-PET-adapted therapy for advanced Hodgkin lymphoma (HL) have clearly demonstrated benefit to alteration of treatment according to interim response, in particular regarding reducing toxicity while maintaining efficacy. However, these studies have differences in design including initial chemotherapy regimen, PET response criteria, patient populations enrolled, and inclusion of radiation, and report different results regarding efficacy and toxicities, which makes cross-trial comparisons difficult. Practitioners are presented with deciding which of these approaches will provide the optimum outcome, balancing toxicity and efficacy, and for which patient with advanced-stage HL. This review summarizes the observations reported from these trials and provides context to help guide physicians and patients in treatment decisions for advanced HL.
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spelling pubmed-72681112020-06-11 PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma Lang, Noemie Crump, Michael Ther Adv Hematol Review Recent results of randomized phase III studies of FDG-PET-adapted therapy for advanced Hodgkin lymphoma (HL) have clearly demonstrated benefit to alteration of treatment according to interim response, in particular regarding reducing toxicity while maintaining efficacy. However, these studies have differences in design including initial chemotherapy regimen, PET response criteria, patient populations enrolled, and inclusion of radiation, and report different results regarding efficacy and toxicities, which makes cross-trial comparisons difficult. Practitioners are presented with deciding which of these approaches will provide the optimum outcome, balancing toxicity and efficacy, and for which patient with advanced-stage HL. This review summarizes the observations reported from these trials and provides context to help guide physicians and patients in treatment decisions for advanced HL. SAGE Publications 2020-06-02 /pmc/articles/PMC7268111/ /pubmed/32537115 http://dx.doi.org/10.1177/2040620720914490 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Lang, Noemie
Crump, Michael
PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma
title PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma
title_full PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma
title_fullStr PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma
title_full_unstemmed PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma
title_short PET-adapted approaches to primary therapy for advanced Hodgkin lymphoma
title_sort pet-adapted approaches to primary therapy for advanced hodgkin lymphoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268111/
https://www.ncbi.nlm.nih.gov/pubmed/32537115
http://dx.doi.org/10.1177/2040620720914490
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