Real-world use of carfilzomib combined with lenalidomide and dexamethasone in patients with multiple myeloma in Europe and Israel.

carfilzomib multiple myeloma proteasome inhibitor real world relapsed/refractory

Journal

EJHaem
ISSN: 2688-6146
Titre abrégé: EJHaem
Pays: United States
ID NLM: 101761942

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 28 09 2022
revised: 29 09 2022
accepted: 29 09 2022
entrez: 23 2 2023
pubmed: 24 2 2023
medline: 24 2 2023
Statut: epublish

Résumé

Clinical trials have demonstrated the efficacy and safety of carfilzomib in patients with relapsed/refractory multiple myeloma (RRMM); however, prospective real-world data are limited. This real-world, prospective, observational study evaluated carfilzomib use, effectiveness and safety in adults with RRMM. Data are presented for a subset of patients (

Identifiants

pubmed: 36819146
doi: 10.1002/jha2.595
pii: JHA2595
pmc: PMC9928790
doi:

Types de publication

Journal Article

Langues

eng

Pagination

174-183

Informations de copyright

© 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

Xavier Leleu received honoraria from Amgen, BMS, CARsgen Therapeutics, Celgene, Gilead, Janssen, Karyopharm Therapeutics, Merck, Oncopeptides, Roche and Takeda. Eirini Katodritou received honoraria and research funding from Amgen and Janssen‐Cilag; held membership on boards of directors or advisory committees for Amgen and Janssen‐Cilag; received expenses and research funding from Genesis Pharma and Takeda; and received research funding from AbbVie and Karyopharm Therapeutics. Thomas Kuehr received consultancy fees and honoraria from Incyte and Janssen; received honoraria and fees to cover travel, accommodation and expenses from Bayer and Lilly; and received honoraria from AbbVie, Amgen, Celgene, Merck, Novartis, Roche and Takeda. Evangelos Terpos received grants, personal fees and non‐financial support from Amgen regarding this work; received grants, personal fees and non‐financial support from Amgen, Celgene/Genesis Pharma, Janssen and Takeda; and received personal fees from AbbVie, BMS, GSK and Novartis, outside the submitted work. Jo Caers received honoraria from Amgen, Celgene, Janssen and Takeda; held membership on boards of directors or advisory committees for Amgen, Celgene, Janssen and Takeda. Renato Zambello held membership on boards of directors or advisory committees for Celgene and Janssen. Alessandra Brescianini is an employee of Amgen and an equity holder. Tony Liang is an employee of Parexel and received funding from Amgen. Sally Wetten was an employee of Amgen and an equity holder at the time of this work. Sorina N. Badelita received consultancy fees, fees to cover travel, accommodation and expenses from Amgen, Janssen and Takeda; and consultancy fees and honoraria from Novartis.

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Auteurs

Xavier Leleu (X)

Department of Haematology University Hospital Centre La Miletrie and Inserm Poitiers France.

Eirini Katodritou (E)

Department of Haematology Theagenio Cancer Hospital Thessaloniki Greece.

Thomas Kuehr (T)

Department of Internal Medicine IV Academic Teaching Hospital Wels-Grieskirchen Wels Austria.

Evangelos Terpos (E)

Department of Clinical Therapeutics, School of Medicine National and Kapodistrian University of Athens Athens Greece.

Jo Caers (J)

Department of Haematology Liège University Hospital Centre Liège Belgium.

Renato Zambello (R)

Department of Medicine Haematology and Clinical Immunology Branch, University of Padua Padua Italy.

Alessandra Brescianini (A)

Research and Development Department Amgen (Europe) GmbH Rotkreuz Switzerland.

Tony Liang (T)

Department of Biostatistics Parexel International Taipei Taiwan.

Sally Wetten (S)

Center for Observational Research Amgen Ltd Uxbridge UK.

Sorina N Badelita (SN)

Department of Hematology Fundeni Clinical Institute Bucharest Romania.

Classifications MeSH