| Literature DB >> 33910333 |
Kwee L Yong1, Samantha Hinsley2, Holger W Auner3, Ceri Bygrave4, Martin F Kaiser5, Karthik Ramasamy6, Ruth M De Tute7, Debbie Sherratt2, Louise Flanagan2, Mamta Garg8, Stephen Hawkins9, Catherine Williams10, Jamie Cavenagh11, Neil K Rabin12, James Croft5, Gareth Morgan13, Faith Davies13, Roger G Owen14, Sarah R Brown2.
Abstract
The proteasome inhibitors (PIs), carfilzomib and bortezomib, are widely used to treat myeloma but head-to-head comparisons have produced conflicting results. We compared the activity of these PIs in combination with cyclophosphamide and dexamethasone (KCd vs VCd) in second line treatment using fixed duration therapy and evaluated the efficacy of carfilzomib maintenance. MUKfive was a phase II controlled, parallel group trial that randomised patients (2:1) to KCd (201) or VCd (99); responding patients on carfilzomib were randomised to maintenance carfilzomib (69) or no further treatment (72). Primary endpoints were (i) very good partial response (VGPR, non-inferiority, OR 0.8) at 24 weeks, and (ii) progression-free survival (PFS). More participants achieved ≥VGPR with carfilzomib compared to bortezomib (40.2% vs. 31.9%, OR=1.48, 90%CI:0.95,2.31; non-inferior), with a trend for particular benefit in adverse risk disease. KCd was associated with higher overall response (≥PR, 84.0% vs. 68.1%, OR=2.72, 90%CI:1.62,4.55, p=0.001). Neuropathy (grade ≥3 or ≥2 with pain) was more common with bortezomib (19.8% vs. 1.5%, p.Entities:
Year: 2021 PMID: 33910333 DOI: 10.3324/haematol.2021.278399
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941