| Literature DB >> 33415072 |
Alessandro Gozzetti1, Francesca Bacchiarri1, Vincenzo Sammartano1, Marzia Defina1, Anna Sicuranza1, Bianca Mecacci1, Elisabetta Zappone1, Emanuele Cencini1, Alberto Fabbri1, Donatella Raspadori1, Monica Bocchia1.
Abstract
Multiple myeloma survival has significantly improved in recent years, due to novel agents that are available for treatment. The anti-CD38 monoclonal antibody Daratumumab is particularly efficient for patients with relapse/refractory disease, and many studies have shown its unprecedented efficacy also as a first treatment. However, to avoid the incidence of infusion reactions, long infusion schedules of 8 h at first dose and 4 h in the following doses are required, which can reduce the compliance of patients and health care professionals. A reduced infusion time of 90 min has been reported previously, but data are missing on the prolonged safety of this over time as well as the efficacy of this approach. In this work, we investigate the safety of 484 rapid Daratumumab infusions given early after the second dose over a 22 months period in 39 myeloma patients.Entities:
Keywords: Daratumumab; efficacy; multiple myeloma; rapid infusion; safety
Year: 2020 PMID: 33415072 PMCID: PMC7783633 DOI: 10.3389/fonc.2020.570187
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244