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New Developments in Myeloma Treatment and Response Assessment

Recent innovative strategies have dramatically redefined the therapeutic landscape for treating multiple myeloma patients. In particular, the development and application of immunotherapy and high-dose therapy have demonstrated high response rates and have prolonged remission duration. Over the past...

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Autores principales: Kraeber-Bodéré, Françoise, Jamet, Bastien, Bezzi, Davide, Zamagni, Elena, Moreau, Philippe, Nanni, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Nuclear Medicine 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478822/
https://www.ncbi.nlm.nih.gov/pubmed/37591548
http://dx.doi.org/10.2967/jnumed.122.264972
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author Kraeber-Bodéré, Françoise
Jamet, Bastien
Bezzi, Davide
Zamagni, Elena
Moreau, Philippe
Nanni, Cristina
author_facet Kraeber-Bodéré, Françoise
Jamet, Bastien
Bezzi, Davide
Zamagni, Elena
Moreau, Philippe
Nanni, Cristina
author_sort Kraeber-Bodéré, Françoise
collection PubMed
description Recent innovative strategies have dramatically redefined the therapeutic landscape for treating multiple myeloma patients. In particular, the development and application of immunotherapy and high-dose therapy have demonstrated high response rates and have prolonged remission duration. Over the past decade, new morphologic or hybrid imaging techniques have gradually replaced conventional skeletal surveys. PET/CT using (18)F-FDG is a powerful imaging tool for the workup at diagnosis and for therapeutic evaluation allowing medullary and extramedullary assessment. The independent negative prognostic value for progression-free and overall survival derived from baseline PET-derived parameters such as the presence of extramedullary disease or paramedullary disease, as well as the number of focal bone lesions and SUV(max), has been reported in several large prospective studies. During therapeutic evaluation, (18)F-FDG PET/CT is considered the reference imaging technique because it can be performed much earlier than MRI, which lacks specificity. Persistence of significant abnormal (18)F-FDG uptake after therapy is an independent negative prognostic factor, and (18)F-FDG PET/CT and medullary flow cytometry are complementary tools for detecting minimal residual disease before maintenance therapy. The definition of a PET metabolic complete response has recently been standardized and the interpretation criteria harmonized. The development of advanced PET analysis and radiomics using machine learning, as well as hybrid imaging with PET/MRI, offers new perspectives for multiple myeloma imaging. Most recently, innovative radiopharmaceuticals such as C-X-C chemokine receptor type 4–targeted small molecules and anti-CD38 radiolabeled antibodies have shown promising results for tumor phenotype imaging and as potential theranostics.
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spelling pubmed-104788222023-09-06 New Developments in Myeloma Treatment and Response Assessment Kraeber-Bodéré, Françoise Jamet, Bastien Bezzi, Davide Zamagni, Elena Moreau, Philippe Nanni, Cristina J Nucl Med Continuing Education Recent innovative strategies have dramatically redefined the therapeutic landscape for treating multiple myeloma patients. In particular, the development and application of immunotherapy and high-dose therapy have demonstrated high response rates and have prolonged remission duration. Over the past decade, new morphologic or hybrid imaging techniques have gradually replaced conventional skeletal surveys. PET/CT using (18)F-FDG is a powerful imaging tool for the workup at diagnosis and for therapeutic evaluation allowing medullary and extramedullary assessment. The independent negative prognostic value for progression-free and overall survival derived from baseline PET-derived parameters such as the presence of extramedullary disease or paramedullary disease, as well as the number of focal bone lesions and SUV(max), has been reported in several large prospective studies. During therapeutic evaluation, (18)F-FDG PET/CT is considered the reference imaging technique because it can be performed much earlier than MRI, which lacks specificity. Persistence of significant abnormal (18)F-FDG uptake after therapy is an independent negative prognostic factor, and (18)F-FDG PET/CT and medullary flow cytometry are complementary tools for detecting minimal residual disease before maintenance therapy. The definition of a PET metabolic complete response has recently been standardized and the interpretation criteria harmonized. The development of advanced PET analysis and radiomics using machine learning, as well as hybrid imaging with PET/MRI, offers new perspectives for multiple myeloma imaging. Most recently, innovative radiopharmaceuticals such as C-X-C chemokine receptor type 4–targeted small molecules and anti-CD38 radiolabeled antibodies have shown promising results for tumor phenotype imaging and as potential theranostics. Society of Nuclear Medicine 2023-09 /pmc/articles/PMC10478822/ /pubmed/37591548 http://dx.doi.org/10.2967/jnumed.122.264972 Text en © 2023 by the Society of Nuclear Medicine and Molecular Imaging. https://creativecommons.org/licenses/by/4.0/Immediate Open Access: Creative Commons Attribution 4.0 International License (CC BY) allows users to share and adapt with attribution, excluding materials credited to previous publications. License: https://creativecommons.org/licenses/by/4.0/. Details: http://jnm.snmjournals.org/site/misc/permission.xhtml
spellingShingle Continuing Education
Kraeber-Bodéré, Françoise
Jamet, Bastien
Bezzi, Davide
Zamagni, Elena
Moreau, Philippe
Nanni, Cristina
New Developments in Myeloma Treatment and Response Assessment
title New Developments in Myeloma Treatment and Response Assessment
title_full New Developments in Myeloma Treatment and Response Assessment
title_fullStr New Developments in Myeloma Treatment and Response Assessment
title_full_unstemmed New Developments in Myeloma Treatment and Response Assessment
title_short New Developments in Myeloma Treatment and Response Assessment
title_sort new developments in myeloma treatment and response assessment
topic Continuing Education
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478822/
https://www.ncbi.nlm.nih.gov/pubmed/37591548
http://dx.doi.org/10.2967/jnumed.122.264972
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