Daratumumab, Bortezomib, and Dexamethasone Versus Bortezomib and Dexamethasone in Patients With Previously Treated Multiple Myeloma: Three-year Follow-up of CASTOR.


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:
08 2020
Historique:
received: 01 07 2019
revised: 23 08 2019
accepted: 29 09 2019
pubmed: 3 6 2020
medline: 21 8 2021
entrez: 3 6 2020
Statut: ppublish

Résumé

In the phase III CASTOR study in relapsed or refractory multiple myeloma, daratumumab, bortezomib, and dexamethasone (D-Vd) demonstrated significant clinical benefit versus Vd alone. Outcomes after 40.0 months of median follow-up are discussed. Eligible patients had received ≥ 1 line of treatment and were administered bortezomib (1.3 mg/m Of 498 patients in the intent-to-treat (ITT) population (D-Vd, n = 251; Vd, n = 247), 47% had 1 prior line of treatment (1PL; D-Vd, n = 122; Vd, n = 113). Median progression-free survival (PFS) was significantly prolonged with D-Vd versus Vd in the ITT population (16.7 vs. 7.1 months; hazard ratio [HR], 0.31; 95% confidence interval [CI], 0.25-0.40; P < .0001) and the 1PL subgroup (27.0 vs. 7.9 months; HR, 0.22; 95% CI, 0.15-0.32; P < .0001). In lenalidomide-refractory patients, the median PFS was 7.8 versus 4.9 months (HR, 0.44; 95% CI, 0.28-0.68; P = .0002) for D-Vd (n = 60) versus Vd (n = 81). Minimal residual disease (MRD)-negativity rates (10 After 3 years, D-Vd maintained significant benefits in patients with relapsed or refractory multiple myeloma with a consistent safety profile. D-Vd provided the greatest benefit at first relapse and increased MRD-negativity rates.

Sections du résumé

BACKGROUND
In the phase III CASTOR study in relapsed or refractory multiple myeloma, daratumumab, bortezomib, and dexamethasone (D-Vd) demonstrated significant clinical benefit versus Vd alone. Outcomes after 40.0 months of median follow-up are discussed.
PATIENTS AND METHODS
Eligible patients had received ≥ 1 line of treatment and were administered bortezomib (1.3 mg/m
RESULTS
Of 498 patients in the intent-to-treat (ITT) population (D-Vd, n = 251; Vd, n = 247), 47% had 1 prior line of treatment (1PL; D-Vd, n = 122; Vd, n = 113). Median progression-free survival (PFS) was significantly prolonged with D-Vd versus Vd in the ITT population (16.7 vs. 7.1 months; hazard ratio [HR], 0.31; 95% confidence interval [CI], 0.25-0.40; P < .0001) and the 1PL subgroup (27.0 vs. 7.9 months; HR, 0.22; 95% CI, 0.15-0.32; P < .0001). In lenalidomide-refractory patients, the median PFS was 7.8 versus 4.9 months (HR, 0.44; 95% CI, 0.28-0.68; P = .0002) for D-Vd (n = 60) versus Vd (n = 81). Minimal residual disease (MRD)-negativity rates (10
CONCLUSION
After 3 years, D-Vd maintained significant benefits in patients with relapsed or refractory multiple myeloma with a consistent safety profile. D-Vd provided the greatest benefit at first relapse and increased MRD-negativity rates.

Identifiants

pubmed: 32482541
pii: S2152-2650(19)32010-5
doi: 10.1016/j.clml.2019.09.623
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
daratumumab 4Z63YK6E0E
Bortezomib 69G8BD63PP
Dexamethasone 7S5I7G3JQL

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

509-518

Informations de copyright

Copyright © 2019 Janssen Global Services, LLC. Published by Elsevier Inc. All rights reserved.

Auteurs

Maria-Victoria Mateos (MV)

Department of Hematology, University Hospital of Salamanca/IBSAL, Salamanca, Spain.

Pieter Sonneveld (P)

Department of Hematology, Erasmus MC, Rotterdam, The Netherlands.

Vania Hungria (V)

Irmandade Da Santa Casa De Misericordia De São Paulo, São Paulo, Brazil.

Ajay K Nooka (AK)

Winship Cancer Institute, Emory University, Atlanta, GA.

Jane A Estell (JA)

Haematology Department, Concord Cancer Centre, Concord Hospital, University of Sydney, Concord NSW, Australia.

Wolney Barreto (W)

Hospital Santa Marcelina, São Paulo, Brazil.

Paolo Corradini (P)

Fondazione IRCCS Instituto Nazionale dei Tumori, Milan, Italy.

Chang-Ki Min (CK)

Seoul St. Mary's Hospital, Seoul, The Republic of Korea.

Eva Medvedova (E)

Oregon Health & Science University, Portland, OR.

Katja Weisel (K)

University Medical Center of Hamburg-Eppendorf, Hamburg, Germany.

Christopher Chiu (C)

Janssen Research & Development, LLC, Spring House, PA.

Jordan M Schecter (JM)

Janssen Research & Development, LLC, Raritan, NJ.

Himal Amin (H)

Janssen Research & Development, LLC, Raritan, NJ.

Xiang Qin (X)

Janssen Research & Development, LLC, Spring House, PA.

Jon Ukropec (J)

Janssen Research & Development, LLC, Spring House, PA.

Rachel Kobos (R)

Janssen Research & Development, LLC, Spring House, PA.

Andrew Spencer (A)

Malignant Haematology and Stem Cell Transplantation Service, Alfred Health-Monash University, Melbourne, Australia. Electronic address: aspencer@netspace.net.au.

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Classifications MeSH