Three Drug Combinations in the Treatment of Fit Elderly Multiple Myeloma Patients.

elderly frailty multiple myeloma survival treatment

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
04 Nov 2020
Historique:
received: 13 10 2020
revised: 30 10 2020
accepted: 02 11 2020
entrez: 7 11 2020
pubmed: 8 11 2020
medline: 8 11 2020
Statut: epublish

Résumé

The multiple myeloma (MM) non transplant eligible (NTE) population is growing in line with the aging of the population in Western countries. Historically, this population has been known for having a greater risk of treatment related toxicity, and therefore drug development was slow and rather oriented towards the improvement of safety profile than the optimization of disease control. However, NTE MM patients, at least for the fit/non frail patients in recent years, seemed to have benefited more from a less palliative care to improve the depth of response and then prolong survival. NTE MM being a quite heterogeneous population, there are still a number of groups of patients that are in need of more efficient therapy, avoiding unnecessary toxicity, particularly for the frail patients. The use of triplet regimen with a melphalan-prednisone (MP) backbone has long been the standard of care for NTE MM, often dedicated to non-frail patients. New standards of care, triplet, and even quadruplet combinations, are emerging on the basis of the MP backbone but also on the more recently approved lenalidomide-dexamethasone (Rd) backbone. These developments were largely possible in line with the development of antibody-based immunotherapies (IT) in MM. The objective to improve outcomes with an acceptable safety profile will see other key therapeutic developments such as the dropping of dexamethasone early in the disease course or various attempts to allow permanent treatment discontinuation with a prolonged disease control. In that context, it is possible that immunomonitoring, minimal residual disease (MRD), and genomic risk-adaptation will become key elements of the treatment decisions on triplet-based regimens.

Identifiants

pubmed: 33158277
pii: jcm9113554
doi: 10.3390/jcm9113554
pmc: PMC7694236
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Hélène Gardeney (H)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Arthur Bobin (A)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Cécile Gruchet (C)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Florence Sabirou (F)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Anthony Lévy (A)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Laly Nsiala (L)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Laura Cailly (L)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Cécile Tomowiak (C)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Jose Torregrosa (J)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Niels Moya (N)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Cyrille Hulin (C)

Service d'Hématologie et de Thérapie Cellulaire, CHU de Bordeaux, 33000 Bordeaux, France.

Xavier Leleu (X)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.
Service d'Hématologie et Thérapie Cellulaire, Universite de Medecine et Pharmacie, 33000 Poitiers, France.

Stéphanie Guidez (S)

Service d'Hematologie et Therapie Cellulaire, and Inserm CIC U1402, 86000 Poitiers, France.

Classifications MeSH