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FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas

PET using (18)F-FDG for treatment monitoring in patients with lymphoma is one of the most well-developed clinical applications. PET/CT is nowadays used during treatment to assess chemosensitivity, with response-adapted therapy given according to ‘interim’ PET in clinical practice to adults and child...

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Autores principales: Barrington, Sally F., Kluge, Regine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541086/
https://www.ncbi.nlm.nih.gov/pubmed/28411336
http://dx.doi.org/10.1007/s00259-017-3690-8
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author Barrington, Sally F.
Kluge, Regine
author_facet Barrington, Sally F.
Kluge, Regine
author_sort Barrington, Sally F.
collection PubMed
description PET using (18)F-FDG for treatment monitoring in patients with lymphoma is one of the most well-developed clinical applications. PET/CT is nowadays used during treatment to assess chemosensitivity, with response-adapted therapy given according to ‘interim’ PET in clinical practice to adults and children with Hodgkin lymphoma. PET is also used to assess remission from disease and to predict prognosis in the pretransplant setting. Mature data have been reported for the common subtypes of aggressive B-cell lymphomas, with more recent data also supporting the use of PET for response assessment in T-cell lymphomas. The Deauville five-point scale incorporating the Deauville criteria (DC) is recommended for response assessment in international guidelines. FDG uptake is graded in relation to the reference regions of normal mediastinum and liver. The DC have been validated in most lymphoma subtypes. The DC permit the threshold for adequate or inadequate response to be adapted according to the clinical context or research question. It is important for PET readers to understand how the DC have been applied in response-adapted trials for correct interpretation and discussion with the multidisciplinary team. Quantitative methods to perform PET in standardized ways have also been developed which may further improve response assessment including a quantitative extension to the DC (qPET). This may have advantages in providing a continuous scale to refine the threshold for adequate/inadequate response in specific clinical situations or treatment optimization in trials. qPET is also less observer-dependent and limits the problem of optical misinterpretation due to the influence of background activity.
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spelling pubmed-55410862017-08-17 FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas Barrington, Sally F. Kluge, Regine Eur J Nucl Med Mol Imaging Review Article PET using (18)F-FDG for treatment monitoring in patients with lymphoma is one of the most well-developed clinical applications. PET/CT is nowadays used during treatment to assess chemosensitivity, with response-adapted therapy given according to ‘interim’ PET in clinical practice to adults and children with Hodgkin lymphoma. PET is also used to assess remission from disease and to predict prognosis in the pretransplant setting. Mature data have been reported for the common subtypes of aggressive B-cell lymphomas, with more recent data also supporting the use of PET for response assessment in T-cell lymphomas. The Deauville five-point scale incorporating the Deauville criteria (DC) is recommended for response assessment in international guidelines. FDG uptake is graded in relation to the reference regions of normal mediastinum and liver. The DC have been validated in most lymphoma subtypes. The DC permit the threshold for adequate or inadequate response to be adapted according to the clinical context or research question. It is important for PET readers to understand how the DC have been applied in response-adapted trials for correct interpretation and discussion with the multidisciplinary team. Quantitative methods to perform PET in standardized ways have also been developed which may further improve response assessment including a quantitative extension to the DC (qPET). This may have advantages in providing a continuous scale to refine the threshold for adequate/inadequate response in specific clinical situations or treatment optimization in trials. qPET is also less observer-dependent and limits the problem of optical misinterpretation due to the influence of background activity. Springer Berlin Heidelberg 2017-04-14 2017 /pmc/articles/PMC5541086/ /pubmed/28411336 http://dx.doi.org/10.1007/s00259-017-3690-8 Text en © The Author(s) 2017 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 Review Article
Barrington, Sally F.
Kluge, Regine
FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas
title FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas
title_full FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas
title_fullStr FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas
title_full_unstemmed FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas
title_short FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas
title_sort fdg pet for therapy monitoring in hodgkin and non-hodgkin lymphomas
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541086/
https://www.ncbi.nlm.nih.gov/pubmed/28411336
http://dx.doi.org/10.1007/s00259-017-3690-8
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