Safety of ninety-minute daratumumab infusion.
Multiple myeloma
daratumumab
infusion related reaction
safety
Journal
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372
Informations de publication
Date de publication:
Jul 2021
Jul 2021
Historique:
pubmed:
1
9
2020
medline:
22
7
2021
entrez:
1
9
2020
Statut:
ppublish
Résumé
Daratumumab is the first anti-CD38 monoclonal antibody of the class approved for recurrent and refractory multiple myeloma. Grade 3 and 4 Infusion-Related Reactions (IRRs) are frequent during the first and second infusions. Due to the risks associated with severe IRRs, daratumumab is systematically administered over a period of 3.5 hours.The main objective of this study was to evaluate the safety of a 90-minute daratumumab infusion from the third infusion. All patients who had received two or more doses of daratumumab in monotherapy or in combination with standard infusion rates were included. We excluded patients enrolled in clinical trials. For the rapid infusion protocol, 20% of the dose was administered over 30 minutes and the remaining 80% over 60 minutes. From April 1 to May 31, 2019, 25 patients received 53 90-minute infusions of daratumumab. Premedication included corticosteroids, antipyretics, antihistamines, and if necessary a leukotriene receptor antagonist. No grade 3 or grade 4 IRRs were observed. From the third infusion, we found that a rapid administration of daratumumab (90 vs 210 minutes) was well tolerated and safe. It would be interesting to test this regimen from the second infusion.
Identifiants
pubmed: 32865161
doi: 10.1177/1078155220951231
doi:
Substances chimiques
Antibodies, Monoclonal
0
Antineoplastic Agents
0
daratumumab
4Z63YK6E0E
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM