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Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma

Multiple myeloma (MM) is always preceded by an initial monoclonal gammopathy of undetermined significance (MGUS) that then develops into asymptomatic or smoldering multiple myeloma (SMM), which constitutes an intermediate clinical stage between MGUS and MM. According to a recent study, risk factors...

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Autores principales: Jamet, Bastien, Bailly, Clément, Carlier, Thomas, Touzeau, Cyrille, Michaud, Anne-Victoire, Bourgeois, Mickael, Moreau, Philippe, Bodet-Milin, Caroline, Kraeber-Bodere, Françoise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072331/
https://www.ncbi.nlm.nih.gov/pubmed/32092901
http://dx.doi.org/10.3390/cancers12020486
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author Jamet, Bastien
Bailly, Clément
Carlier, Thomas
Touzeau, Cyrille
Michaud, Anne-Victoire
Bourgeois, Mickael
Moreau, Philippe
Bodet-Milin, Caroline
Kraeber-Bodere, Françoise
author_facet Jamet, Bastien
Bailly, Clément
Carlier, Thomas
Touzeau, Cyrille
Michaud, Anne-Victoire
Bourgeois, Mickael
Moreau, Philippe
Bodet-Milin, Caroline
Kraeber-Bodere, Françoise
author_sort Jamet, Bastien
collection PubMed
description Multiple myeloma (MM) is always preceded by an initial monoclonal gammopathy of undetermined significance (MGUS) that then develops into asymptomatic or smoldering multiple myeloma (SMM), which constitutes an intermediate clinical stage between MGUS and MM. According to a recent study, risk factors for faster MGUS to MM progression include an M protein of 1.5 g/dL or more and an abnormal free light chain ratio in patients with non-IgM MGUS. Therefore, the International Myeloma Working Group (IMWG) decided to recommend whole-body computed tomography (WBCT) for patients with high-risk MGUS in order to exclude early bone destruction. Studies evaluating magnetic resonance imaging (MRI) in SMM found an optimal cutoff of two or more focal lesions to be of prognostic significance for fast progression into symptomatic disease and considered this biomarker as a myeloma-defining event (MDE) needing to start therapy with the aim to avoid progression to harmful bone lesions. Moreover, studies assessing positron emission tomography (PET) with computed tomography (CT) using 18F-deoxyglucose (FDG) (FDG-PET/CT) in SMM showed that presence of focal bone lesion without underlying osteolysis is associated with a rapid progression to symptomatic MM. Latest IMWG guidelines recommended to perform WBCT (either CT alone or as part of an FDG-PET/CT protocol) as the first imaging technique at suspected SMM and, if these images are negative or inconclusive, to perform whole-body MRI. The goal of this paper is to clarify the role of different imaging modalities in MGUS and SMM workups.
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spelling pubmed-70723312020-03-19 Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma Jamet, Bastien Bailly, Clément Carlier, Thomas Touzeau, Cyrille Michaud, Anne-Victoire Bourgeois, Mickael Moreau, Philippe Bodet-Milin, Caroline Kraeber-Bodere, Françoise Cancers (Basel) Review Multiple myeloma (MM) is always preceded by an initial monoclonal gammopathy of undetermined significance (MGUS) that then develops into asymptomatic or smoldering multiple myeloma (SMM), which constitutes an intermediate clinical stage between MGUS and MM. According to a recent study, risk factors for faster MGUS to MM progression include an M protein of 1.5 g/dL or more and an abnormal free light chain ratio in patients with non-IgM MGUS. Therefore, the International Myeloma Working Group (IMWG) decided to recommend whole-body computed tomography (WBCT) for patients with high-risk MGUS in order to exclude early bone destruction. Studies evaluating magnetic resonance imaging (MRI) in SMM found an optimal cutoff of two or more focal lesions to be of prognostic significance for fast progression into symptomatic disease and considered this biomarker as a myeloma-defining event (MDE) needing to start therapy with the aim to avoid progression to harmful bone lesions. Moreover, studies assessing positron emission tomography (PET) with computed tomography (CT) using 18F-deoxyglucose (FDG) (FDG-PET/CT) in SMM showed that presence of focal bone lesion without underlying osteolysis is associated with a rapid progression to symptomatic MM. Latest IMWG guidelines recommended to perform WBCT (either CT alone or as part of an FDG-PET/CT protocol) as the first imaging technique at suspected SMM and, if these images are negative or inconclusive, to perform whole-body MRI. The goal of this paper is to clarify the role of different imaging modalities in MGUS and SMM workups. MDPI 2020-02-19 /pmc/articles/PMC7072331/ /pubmed/32092901 http://dx.doi.org/10.3390/cancers12020486 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jamet, Bastien
Bailly, Clément
Carlier, Thomas
Touzeau, Cyrille
Michaud, Anne-Victoire
Bourgeois, Mickael
Moreau, Philippe
Bodet-Milin, Caroline
Kraeber-Bodere, Françoise
Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma
title Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma
title_full Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma
title_fullStr Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma
title_full_unstemmed Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma
title_short Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma
title_sort imaging of monoclonal gammapathy of undetermined significance and smoldering multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072331/
https://www.ncbi.nlm.nih.gov/pubmed/32092901
http://dx.doi.org/10.3390/cancers12020486
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