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Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment
PURPOSE: To determine whether, in patients with Hodgkin lymphoma (HL) or non-Hodgkin lymphoma (NHL), [(18)F]FDG PET/MR can capture treatment effects within the first week after treatment initiation, and whether changes in glucose metabolism and cell density occur simultaneously. METHODS: Patients wi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915494/ https://www.ncbi.nlm.nih.gov/pubmed/29480328 http://dx.doi.org/10.1007/s00259-018-3937-z |
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author | Mayerhoefer, Marius E. Raderer, Markus Jaeger, Ulrich Staber, Philipp Kiesewetter, Barbara Senn, Daniela Gallagher, Ferdia A. Brindle, Kevin Porpaczy, Edit Weber, Michael Berzaczy, Dominik Simonitsch-Klupp, Ingrid Sillaber, Christian Skrabs, Cathrin Haug, Alexander |
author_facet | Mayerhoefer, Marius E. Raderer, Markus Jaeger, Ulrich Staber, Philipp Kiesewetter, Barbara Senn, Daniela Gallagher, Ferdia A. Brindle, Kevin Porpaczy, Edit Weber, Michael Berzaczy, Dominik Simonitsch-Klupp, Ingrid Sillaber, Christian Skrabs, Cathrin Haug, Alexander |
author_sort | Mayerhoefer, Marius E. |
collection | PubMed |
description | PURPOSE: To determine whether, in patients with Hodgkin lymphoma (HL) or non-Hodgkin lymphoma (NHL), [(18)F]FDG PET/MR can capture treatment effects within the first week after treatment initiation, and whether changes in glucose metabolism and cell density occur simultaneously. METHODS: Patients with histologically proven HL or NHL were included in this prospective IRB-approved study. Patients underwent [(18)F]FDG PET/MR before, and then 48–72 h after (follow-up 1, FU-1) and 1 week after (FU-2) initiation of the first cycle of their respective standard chemotherapy (for HL) or immunochemotherapy (for NHL). Standardized [(18)F]FDG uptake values (SUVmax, SUVmean) and apparent diffusion coefficients (ADCmin, ADCmean) based on diffusion-weighted MRI, and metabolic and morphological tumour volumes (MTV, VOL) were assessed at each time-point. Multilevel analyses with an unstructured covariance matrix, and pair-wise post-hoc tests were used to test for significant changes in SUVs, ADCs, MTVs and VOLs between the three time-points. RESULTS: A total of 58 patients (11 with HL and 47 with NHL) with 166 lesions were analysed. Lesion-based mean rates of change in SUVmax, SUVmean, ADCmin, ADCmean, MTV and VOL between baseline and FU-1 were −46.8%, −33.3%, +20.3%, +14%, −46% and −12.8%, respectively, and between baseline and FU-2 were −65.1%, −49%, +50.7%, +32.4%, −61.1% and −24.2%, respectively. These changes were statistically significant (P < 0.01) except for the change in VOL between baseline and FU-1 (P = 0.079). CONCLUSION: In lymphoma patients, [(18)F]FDG PET/MR can capture treatment-induced changes in glucose metabolism and cell density as early as 48–72 h after treatment initiation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00259-018-3937-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5915494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-59154942018-04-30 Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment Mayerhoefer, Marius E. Raderer, Markus Jaeger, Ulrich Staber, Philipp Kiesewetter, Barbara Senn, Daniela Gallagher, Ferdia A. Brindle, Kevin Porpaczy, Edit Weber, Michael Berzaczy, Dominik Simonitsch-Klupp, Ingrid Sillaber, Christian Skrabs, Cathrin Haug, Alexander Eur J Nucl Med Mol Imaging Original Article PURPOSE: To determine whether, in patients with Hodgkin lymphoma (HL) or non-Hodgkin lymphoma (NHL), [(18)F]FDG PET/MR can capture treatment effects within the first week after treatment initiation, and whether changes in glucose metabolism and cell density occur simultaneously. METHODS: Patients with histologically proven HL or NHL were included in this prospective IRB-approved study. Patients underwent [(18)F]FDG PET/MR before, and then 48–72 h after (follow-up 1, FU-1) and 1 week after (FU-2) initiation of the first cycle of their respective standard chemotherapy (for HL) or immunochemotherapy (for NHL). Standardized [(18)F]FDG uptake values (SUVmax, SUVmean) and apparent diffusion coefficients (ADCmin, ADCmean) based on diffusion-weighted MRI, and metabolic and morphological tumour volumes (MTV, VOL) were assessed at each time-point. Multilevel analyses with an unstructured covariance matrix, and pair-wise post-hoc tests were used to test for significant changes in SUVs, ADCs, MTVs and VOLs between the three time-points. RESULTS: A total of 58 patients (11 with HL and 47 with NHL) with 166 lesions were analysed. Lesion-based mean rates of change in SUVmax, SUVmean, ADCmin, ADCmean, MTV and VOL between baseline and FU-1 were −46.8%, −33.3%, +20.3%, +14%, −46% and −12.8%, respectively, and between baseline and FU-2 were −65.1%, −49%, +50.7%, +32.4%, −61.1% and −24.2%, respectively. These changes were statistically significant (P < 0.01) except for the change in VOL between baseline and FU-1 (P = 0.079). CONCLUSION: In lymphoma patients, [(18)F]FDG PET/MR can capture treatment-induced changes in glucose metabolism and cell density as early as 48–72 h after treatment initiation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00259-018-3937-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-02-26 2018 /pmc/articles/PMC5915494/ /pubmed/29480328 http://dx.doi.org/10.1007/s00259-018-3937-z Text en © The Author(s) 2018 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 | Original Article Mayerhoefer, Marius E. Raderer, Markus Jaeger, Ulrich Staber, Philipp Kiesewetter, Barbara Senn, Daniela Gallagher, Ferdia A. Brindle, Kevin Porpaczy, Edit Weber, Michael Berzaczy, Dominik Simonitsch-Klupp, Ingrid Sillaber, Christian Skrabs, Cathrin Haug, Alexander Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
title | Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
title_full | Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
title_fullStr | Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
title_full_unstemmed | Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
title_short | Ultra-early response assessment in lymphoma treatment: [(18)F]FDG PET/MR captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
title_sort | ultra-early response assessment in lymphoma treatment: [(18)f]fdg pet/mr captures changes in glucose metabolism and cell density within the first 72 hours of treatment |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915494/ https://www.ncbi.nlm.nih.gov/pubmed/29480328 http://dx.doi.org/10.1007/s00259-018-3937-z |
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