High-risk smoldering myeloma versus early detection of multiple myeloma: Current models, goals of therapy, and clinical implications.


Journal

Best practice & research. Clinical haematology
ISSN: 1532-1924
Titre abrégé: Best Pract Res Clin Haematol
Pays: Netherlands
ID NLM: 101120659

Informations de publication

Date de publication:
03 2020
Historique:
received: 21 01 2020
accepted: 23 01 2020
entrez: 7 3 2020
pubmed: 7 3 2020
medline: 18 12 2020
Statut: ppublish

Résumé

Multiple myeloma, a bone marrow cancer, is preceded by precursor stages called monoclonal gammopathy of unknown significance and smoldering multiple myeloma. Over the past few years, highly effective and safe therapies have been made available to treat multiple myeloma. This represents a major breakthrough and has major therapeutic implications. Treatment for multiple myeloma has evolved to include treatment of precursor stages (early treatment) as these therapies are shown to be safe and effective also in smoldering myeloma. Randomized studies have shown that early treatment can delay the onset of multiple myeloma and even improve overall survival compared to observation in smoldering myeloma. The best therapeutic course and selection of patients with smoldering myeloma to treat is still a matter of debate. In this manuscript, we review the definition, management, clinical implications of smoldering myeloma and early detection of myeloma in the current context and with up-to-date data.

Identifiants

pubmed: 32139017
pii: S1521-6926(20)30013-X
doi: 10.1016/j.beha.2020.101152
pmc: PMC7069728
mid: NIHMS1556260
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antibodies, Monoclonal, Humanized 0
Oligopeptides 0
daratumumab 4Z63YK6E0E
carfilzomib 72X6E3J5AR
Dexamethasone 7S5I7G3JQL
Lenalidomide F0P408N6V4
isatuximab R30772KCU0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

101152

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest C. Kunacheewa reports no conflicts of interest. E. Manasanch has received research support from Sanofi, Quest Diagnostics, Novartis, JW. Pharma, Merck; consultant fees from Celgene, Janssen, Sanofi and Adaptive Biotechnologies.

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Auteurs

Chutima Kunacheewa (C)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Elisabet E Manasanch (EE)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. Electronic address: eemanasanch@mdanderson.org.

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Classifications MeSH