Response to First Cycle Is the Major Predictor of Long-Term Response to Lenalidomide and Dexamethasone Therapy in Relapsed and Refractory Multiple Myeloma: Can We Spare Patients the Toxicity and Costs of Additional Agents?


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
09 2019
Historique:
received: 15 11 2018
revised: 30 01 2019
accepted: 26 05 2019
pubmed: 1 7 2019
medline: 15 8 2020
entrez: 1 7 2019
Statut: ppublish

Résumé

Lenalidomide plus dexamethasone (Ld) is still considered an option of care for some selected patients with relapsed or refractory multiple myeloma (RRMM), despite the proven superiority of lenalidomide-based triplet therapy. Up to 20% of patients obtain long-term benefit from Ld alone. The aim of this multicenter retrospective study was to identify and characterize those with good response to Ld salvage therapy, defined as progression-free survival lasting more than 24 months. Patients treated with Ld in a consortium of 3 tertiary-care hospitals (Institut Català d'Oncologia) between 2009 and 2016 were prospectively registered; 227 patients had evaluable data. In multivariate analysis, obtaining partial response after the first therapy cycle was the main independent factor associated with progression-free survival lasting more than 24 months. Together with standard risk cytogenetics, partial response after first cycle was also independently associated with a higher rate of complete response. Previous plasma-cell dyscrasia remained as the only baseline characteristic independently associated with long-lasting responses. High-risk cytogenetics and no history of monoclonal gammopathy of undetermined significance were the only statistically significant negative prognostic factors for overall survival. Patients who had received only one prior therapy showed a trend toward higher overall survival. If Ld is to be considered a treatment choice, at least a partial response should be obtained after the first therapy cycle to maintain double-agent therapy safely.

Sections du résumé

BACKGROUND
Lenalidomide plus dexamethasone (Ld) is still considered an option of care for some selected patients with relapsed or refractory multiple myeloma (RRMM), despite the proven superiority of lenalidomide-based triplet therapy. Up to 20% of patients obtain long-term benefit from Ld alone. The aim of this multicenter retrospective study was to identify and characterize those with good response to Ld salvage therapy, defined as progression-free survival lasting more than 24 months.
PATIENTS AND METHODS
Patients treated with Ld in a consortium of 3 tertiary-care hospitals (Institut Català d'Oncologia) between 2009 and 2016 were prospectively registered; 227 patients had evaluable data.
RESULTS
In multivariate analysis, obtaining partial response after the first therapy cycle was the main independent factor associated with progression-free survival lasting more than 24 months. Together with standard risk cytogenetics, partial response after first cycle was also independently associated with a higher rate of complete response. Previous plasma-cell dyscrasia remained as the only baseline characteristic independently associated with long-lasting responses. High-risk cytogenetics and no history of monoclonal gammopathy of undetermined significance were the only statistically significant negative prognostic factors for overall survival. Patients who had received only one prior therapy showed a trend toward higher overall survival.
CONCLUSION
If Ld is to be considered a treatment choice, at least a partial response should be obtained after the first therapy cycle to maintain double-agent therapy safely.

Identifiants

pubmed: 31255588
pii: S2152-2650(18)31612-4
doi: 10.1016/j.clml.2019.05.020
pii:
doi:

Substances chimiques

Biomarkers 0
Dexamethasone 7S5I7G3JQL
Lenalidomide F0P408N6V4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

585-592.e1

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Susanna Gassiot (S)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Departament de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain. Electronic address: sgassiot@iconcologia.net.

Yolanda González (Y)

Institut Català d'Oncologia, Hospital Josep Trueta, Girona, Spain.

Mireia Morgades (M)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Badalona, Spain.

Cristina Motlló (C)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Badalona, Spain.

Victòria Clapés (V)

Institut Català d'Oncologia, Hospital Duran i Reynals, L'Hospitalet de Llobregat, Llobregat, Spain.

Clara Maluquer (C)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Badalona, Spain.

Gladys Ibarra (G)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Badalona, Spain.

Laura Abril (L)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Badalona, Spain.

Josep-Maria Ribera (JM)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Departament de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.

Albert Oriol (A)

Institut Català d'Oncologia, Hospital Germans Trias i Pujol, Josep Carreras Leukaemia Research Institute, Departament de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH