How I treat frontline transplantation-eligible multiple myeloma.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
12 05 2022
Historique:
received: 19 05 2021
accepted: 05 11 2021
pubmed: 18 11 2021
medline: 18 5 2022
entrez: 17 11 2021
Statut: ppublish

Résumé

High-dose melphalan supported by autologous transplantation has been the standard of care for eligible patients with newly diagnosed multiple myeloma (MM) for >25 years. Several randomized clinical trials have recently reaffirmed the strong position of transplantation in the era of proteasome inhibitors and immunomodulatory drugs combinations, demonstrating a significant reduction of progression or death in comparison with strategies without transplantation. Immunotherapy is currently changing the paradigm of MM management, and daratumumab is the first-in-class human monoclonal antibody targeting CD38 approved in the setting of newly diagnosed MM. Quadruplets have become the new standard in transplantation programs, but outcomes remain heterogeneous, with various response depth and duration. The development of sensitive and specific tools for disease prognostication allows the consideration of strategies adaptive to dynamic risk. This review discusses the different options available for the treatment of transplantation-eligible patients with MM in frontline setting.

Identifiants

pubmed: 34788422
pii: S0006-4971(21)01881-4
doi: 10.1182/blood.2020008735
doi:

Substances chimiques

Proteasome Inhibitors 0
Bortezomib 69G8BD63PP
Melphalan Q41OR9510P

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2882-2888

Informations de copyright

© 2022 by The American Society of Hematology.

Auteurs

Aurore Perrot (A)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse-Oncopole, and.
Centre de Recherches en Cancérologie de Toulouse, Université de Toulouse, Université Toulouse III Paul Sabatier, INSERM, Toulouse, France.

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Classifications MeSH