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Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma
The goal of this retrospective study was to analyze and compare the prognostic role of fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (2-[(18)F]-FDG PET/CT) features and sarcopenia, estimated by CT of PET in elderly (≥65 years) Mantle Cell Lymphoma (MCL). We recruite...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911178/ https://www.ncbi.nlm.nih.gov/pubmed/35268301 http://dx.doi.org/10.3390/jcm11051210 |
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author | Albano, Domenico Pasinetti, Nadia Dondi, Francesco Giubbini, Raffaele Tucci, Alessandra Bertagna, Francesco |
author_facet | Albano, Domenico Pasinetti, Nadia Dondi, Francesco Giubbini, Raffaele Tucci, Alessandra Bertagna, Francesco |
author_sort | Albano, Domenico |
collection | PubMed |
description | The goal of this retrospective study was to analyze and compare the prognostic role of fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (2-[(18)F]-FDG PET/CT) features and sarcopenia, estimated by CT of PET in elderly (≥65 years) Mantle Cell Lymphoma (MCL). We recruited 53 patients, who underwent pre-treatment 2-[(18)F]-FDG PET/CT and end-of-treatment PET/CT, and the main semiquantitative parameters were calculated. Sarcopenia was measured as skeletal muscle index (SMI, cm(2)/m(2)) and derived by low-dose PET/CT images at the L3 level. Specific cut-offs for SMI were calculated by receiver operator curve and divided by gender. Metabolic response was evaluated at end-of-treatment PET/CT, applying the Deauville score. Progression Free Survival (PFS) and Overall Survival (OS) were calculated for the whole population and for different subgroups, defined as per different sarcopenia cut-off levels. The specific cut-offs to define sarcopenia were 53 cm(2)/m(2) for male and 45.6 cm(2)/m(2) for female. Thirty-two (60%) patients were defined as sarcopenic. The 3-year and 5-year PFS rates were 29% and 23%, while the 3-year and 5-year OS rates were 43% and 33%. Metabolic response, total metabolic tumor volume (tMTV), total lesion glycolysis (tTLG) and sarcopenia were independent prognostic factors for PFS. Considering OS, no variable was significantly associated. Combination between PET features and sarcopenia may help to predict PFS. |
format | Online Article Text |
id | pubmed-8911178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89111782022-03-11 Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma Albano, Domenico Pasinetti, Nadia Dondi, Francesco Giubbini, Raffaele Tucci, Alessandra Bertagna, Francesco J Clin Med Article The goal of this retrospective study was to analyze and compare the prognostic role of fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (2-[(18)F]-FDG PET/CT) features and sarcopenia, estimated by CT of PET in elderly (≥65 years) Mantle Cell Lymphoma (MCL). We recruited 53 patients, who underwent pre-treatment 2-[(18)F]-FDG PET/CT and end-of-treatment PET/CT, and the main semiquantitative parameters were calculated. Sarcopenia was measured as skeletal muscle index (SMI, cm(2)/m(2)) and derived by low-dose PET/CT images at the L3 level. Specific cut-offs for SMI were calculated by receiver operator curve and divided by gender. Metabolic response was evaluated at end-of-treatment PET/CT, applying the Deauville score. Progression Free Survival (PFS) and Overall Survival (OS) were calculated for the whole population and for different subgroups, defined as per different sarcopenia cut-off levels. The specific cut-offs to define sarcopenia were 53 cm(2)/m(2) for male and 45.6 cm(2)/m(2) for female. Thirty-two (60%) patients were defined as sarcopenic. The 3-year and 5-year PFS rates were 29% and 23%, while the 3-year and 5-year OS rates were 43% and 33%. Metabolic response, total metabolic tumor volume (tMTV), total lesion glycolysis (tTLG) and sarcopenia were independent prognostic factors for PFS. Considering OS, no variable was significantly associated. Combination between PET features and sarcopenia may help to predict PFS. MDPI 2022-02-23 /pmc/articles/PMC8911178/ /pubmed/35268301 http://dx.doi.org/10.3390/jcm11051210 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Albano, Domenico Pasinetti, Nadia Dondi, Francesco Giubbini, Raffaele Tucci, Alessandra Bertagna, Francesco Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma |
title | Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma |
title_full | Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma |
title_fullStr | Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma |
title_full_unstemmed | Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma |
title_short | Prognostic Role of Pre-Treatment Metabolic Parameters and Sarcopenia Derived by 2-[(18)F]-FDG PET/CT in Elderly Mantle Cell Lymphoma |
title_sort | prognostic role of pre-treatment metabolic parameters and sarcopenia derived by 2-[(18)f]-fdg pet/ct in elderly mantle cell lymphoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911178/ https://www.ncbi.nlm.nih.gov/pubmed/35268301 http://dx.doi.org/10.3390/jcm11051210 |
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