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PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma

PURPOSE: Childhood RMS is a rare malignant disease in which evaluation of tumour spread at diagnosis is essential for therapeutic management. F-18 FDG-PET imaging is currently used for initial RMS disease staging. MATERIALS AND METHODS: This multicentre retrospective study in six French university h...

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Autores principales: Fayolle, Helio, Jehanno, Nina, Lauwers-Cances, Valerie, Castex, Marie-Pierre, Orbach, Daniel, Mognetti, Thomas, Nadège, Corradini, Payoux, Pierre, Hitzel, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759649/
https://www.ncbi.nlm.nih.gov/pubmed/35030176
http://dx.doi.org/10.1371/journal.pone.0261565
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author Fayolle, Helio
Jehanno, Nina
Lauwers-Cances, Valerie
Castex, Marie-Pierre
Orbach, Daniel
Mognetti, Thomas
Nadège, Corradini
Payoux, Pierre
Hitzel, Anne
author_facet Fayolle, Helio
Jehanno, Nina
Lauwers-Cances, Valerie
Castex, Marie-Pierre
Orbach, Daniel
Mognetti, Thomas
Nadège, Corradini
Payoux, Pierre
Hitzel, Anne
author_sort Fayolle, Helio
collection PubMed
description PURPOSE: Childhood RMS is a rare malignant disease in which evaluation of tumour spread at diagnosis is essential for therapeutic management. F-18 FDG-PET imaging is currently used for initial RMS disease staging. MATERIALS AND METHODS: This multicentre retrospective study in six French university hospitals was designed to analyse the prognostic accuracy of MTV at diagnosis for patients with RMS between 1 January 2007 and 31 October 2017, for overall (OS) and progression-free survival (PFS). MTV was defined as the sum of the primitive tumour and the largest metastasis, where relevant, with a 40% threshold of the primary tumour SUVmax. Additional aims were to define the prognostic value of SUVmax, SUVpeak, and bone lysis at diagnosis. RESULTS: Participants were 101 patients with a median age of 7.4 years (IQR [4.0-12.5], 62 boys), with localized disease (35 cases), regional nodal spread (43 cases), or distant metastases (23). 44 patients had alveolar subtypes. In a univariate analysis, a MTV greater than 200 cm(3) was associated with OS (HR = 3.47 [1.79;6.74], p<0.001) and PFS (HR = 3.03 [1.51;6.07], p = 0.002). SUVmax, SUVpeak, and bone lysis also influenced OS (respectively p = 0.005, p = 0.004 and p = 0.007) and PFS (p = 0.029, p = 0.019 and p = 0.015). In a multivariate analysis, a MTV greater than 200 cm(3) was associated with OS (HR = 2.642 [1.272;5.486], p = 0.009) and PFS (HR = 2.707 [1.322;5.547], p = 0.006) after adjustment for confounding factors, including SUVmax, SUVpeak, and bone lysis. CONCLUSION: A metabolic tumor volume greater than 200 cm(3), SUVmax, SUVpeak, and bone lysis in the pre-treatment assessment were unfavourable for outcome.
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spelling pubmed-87596492022-01-15 PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma Fayolle, Helio Jehanno, Nina Lauwers-Cances, Valerie Castex, Marie-Pierre Orbach, Daniel Mognetti, Thomas Nadège, Corradini Payoux, Pierre Hitzel, Anne PLoS One Research Article PURPOSE: Childhood RMS is a rare malignant disease in which evaluation of tumour spread at diagnosis is essential for therapeutic management. F-18 FDG-PET imaging is currently used for initial RMS disease staging. MATERIALS AND METHODS: This multicentre retrospective study in six French university hospitals was designed to analyse the prognostic accuracy of MTV at diagnosis for patients with RMS between 1 January 2007 and 31 October 2017, for overall (OS) and progression-free survival (PFS). MTV was defined as the sum of the primitive tumour and the largest metastasis, where relevant, with a 40% threshold of the primary tumour SUVmax. Additional aims were to define the prognostic value of SUVmax, SUVpeak, and bone lysis at diagnosis. RESULTS: Participants were 101 patients with a median age of 7.4 years (IQR [4.0-12.5], 62 boys), with localized disease (35 cases), regional nodal spread (43 cases), or distant metastases (23). 44 patients had alveolar subtypes. In a univariate analysis, a MTV greater than 200 cm(3) was associated with OS (HR = 3.47 [1.79;6.74], p<0.001) and PFS (HR = 3.03 [1.51;6.07], p = 0.002). SUVmax, SUVpeak, and bone lysis also influenced OS (respectively p = 0.005, p = 0.004 and p = 0.007) and PFS (p = 0.029, p = 0.019 and p = 0.015). In a multivariate analysis, a MTV greater than 200 cm(3) was associated with OS (HR = 2.642 [1.272;5.486], p = 0.009) and PFS (HR = 2.707 [1.322;5.547], p = 0.006) after adjustment for confounding factors, including SUVmax, SUVpeak, and bone lysis. CONCLUSION: A metabolic tumor volume greater than 200 cm(3), SUVmax, SUVpeak, and bone lysis in the pre-treatment assessment were unfavourable for outcome. Public Library of Science 2022-01-14 /pmc/articles/PMC8759649/ /pubmed/35030176 http://dx.doi.org/10.1371/journal.pone.0261565 Text en © 2022 Fayolle et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fayolle, Helio
Jehanno, Nina
Lauwers-Cances, Valerie
Castex, Marie-Pierre
Orbach, Daniel
Mognetti, Thomas
Nadège, Corradini
Payoux, Pierre
Hitzel, Anne
PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
title PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
title_full PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
title_fullStr PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
title_full_unstemmed PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
title_short PET metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
title_sort pet metabolic tumor volume as a new prognostic factor in childhood rhabdomyosarcoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759649/
https://www.ncbi.nlm.nih.gov/pubmed/35030176
http://dx.doi.org/10.1371/journal.pone.0261565
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