Imaging of Monoclonal Gammapathy of Undetermined Significance and Smoldering Multiple Myeloma.

FDG-PET/CT MGUS MRI SMM WBCT imaging

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
19 Feb 2020
Historique:
received: 28 01 2020
revised: 11 02 2020
accepted: 15 02 2020
entrez: 26 2 2020
pubmed: 26 2 2020
medline: 26 2 2020
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32092901
pii: cancers12020486
doi: 10.3390/cancers12020486
pmc: PMC7072331
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Bastien Jamet (B)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.

Clément Bailly (C)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.
CRCINA, INSERM, CNRS, Angers University, Nantes University, 44093 Nantes, France.

Thomas Carlier (T)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.
CRCINA, INSERM, CNRS, Angers University, Nantes University, 44093 Nantes, France.

Cyrille Touzeau (C)

Haematology Department, University Hospital, 44093 Nantes, France.

Anne-Victoire Michaud (AV)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.

Mickael Bourgeois (M)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.
CRCINA, INSERM, CNRS, Angers University, Nantes University, 44093 Nantes, France.

Philippe Moreau (P)

Haematology Department, University Hospital, 44093 Nantes, France.

Caroline Bodet-Milin (C)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.
CRCINA, INSERM, CNRS, Angers University, Nantes University, 44093 Nantes, France.

Françoise Kraeber-Bodere (F)

Nuclear Medicine Unit, University Hospital, 44093 Nantes, France.
CRCINA, INSERM, CNRS, Angers University, Nantes University, 44093 Nantes, France.
Nuclear Medicine Unit, ICO-Gauducheau, 44805 Nantes-Saint-Herblain, France.

Classifications MeSH