Carfilzomib-based combination regimens are highly effective frontline therapies for multiple myeloma and Waldenström's macroglobulinemia.
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Biomarkers
Female
Humans
Male
Middle Aged
Multiple Myeloma
/ diagnosis
Mutation
Neoplasm Staging
Oligopeptides
/ administration & dosage
Receptors, CXCR4
/ genetics
Remission Induction
Retrospective Studies
Translocation, Genetic
Treatment Outcome
Waldenstrom Macroglobulinemia
/ diagnosis
Myeloma
carfilzomib
efficacy
frontline
toxicity
waldenström
Journal
Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
pubmed:
20
9
2018
medline:
23
6
2020
entrez:
20
9
2018
Statut:
ppublish
Résumé
Multiple myeloma (MM) and Waldenström's macroglobulinemia (WM) are plasma cell disorders often treated with proteasome inhibitors. Recently, several studies evaluated carfilzomib as an initial treatment for these diseases and reported outstanding clinical outcomes. We conducted a retrospective study to report the efficacy and safety of frontline carfilzomib-based combinations in a standard of care setting. From 2014 until 2016 we identified newly diagnosed MM (n = 54) and WM (n = 6) patients treated with carfilzomib as initial therapy who met study inclusion criteria. The response rate for myeloma patients was 98% with 77% of patients undergoing upfront autologous stem cell transplant. The clinical benefit for WM was 100% with all patients having a resolution of B symptoms and anemia after treatment. Carfilzomib-based regimens are well tolerated and offer a neuropathy sparing approach with excellent responses both in newly diagnosed MM and WM making them a good choice for the frontline treatment of these diseases.
Identifiants
pubmed: 30227761
doi: 10.1080/10428194.2018.1508668
doi:
Substances chimiques
Biomarkers
0
CXCR4 protein, human
0
Oligopeptides
0
Receptors, CXCR4
0
carfilzomib
72X6E3J5AR
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
964-970Subventions
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States