Carfilzomib and dexamethasone maintenance following salvage ASCT in multiple myeloma: A randomised phase 2 trial by the Nordic Myeloma Study Group

dc.contributor.authorGregersen Henrik
dc.contributor.authorPeceliunas Valdas
dc.contributor.authorRemes Kari
dc.contributor.authorSchjesvold Fredrik
dc.contributor.authorAbildgaard Niels
dc.contributor.authorNahi Hareth
dc.contributor.authorAndersen Niels Frost
dc.contributor.authorVangsted Annette Juul
dc.contributor.authorKlausen Tobias Wirenfeldt
dc.contributor.authorHelleberg Carsten
dc.contributor.authorCarlson Kristina
dc.contributor.authorFrolund Ulf Christian
dc.contributor.authorAxelsson Per
dc.contributor.authorStromberg Olga
dc.contributor.authorBlimark Cecilie Hveding
dc.contributor.authorCrafoord Jacob
dc.contributor.authorTsykunova Galina
dc.contributor.authorEshoj Henrik Rode
dc.contributor.authorWaage Anders
dc.contributor.authorHansson Markus
dc.contributor.authorGulbrandsen Nina
dc.contributor.organizationfi=lääketieteellinen tiedekunta|en=Faculty of Medicine|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.13290506867
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.converis.publication-id67656258
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/67656258
dc.date.accessioned2022-10-28T13:49:36Z
dc.date.available2022-10-28T13:49:36Z
dc.description.abstract<p><strong>Objective:</strong> We investigated the efficacy and safety of carfilzomib-containing induction before salvage high-dose melphalan with autologous stem-cell transplantation (salvage ASCT) and maintenance with carfilzomib and dexamethasone after salvage ASCT in multiple myeloma.<br></p><p><strong>Methods: </strong>This randomised, open-label, phase 2 trial included patients with first relapse of multiple myeloma after upfront ASCT who were re-induced with four cycles of carfilzomib, cyclophosphamide and dexamethasone. Two months after salvage, ASCT patients were randomised to either observation or maintenance therapy with iv carfilzomib 27 -> 56 mg/sqm and p.o. dexamethasone 20 mg every second week. The study enrolled 200 patients of which 168 were randomised to either maintenance with carfilzomib and dexamethasone (n = 82) or observation (n = 86).</p><p><strong>Results:</strong> Median time to progression (TTP) after randomisation was 25.1 months (22.5-NR) in the carfilzomib-dexamethasone maintenance group and 16.7 months (14.4-21.8) in the control group (HR 0.46, 95% CI 0.30-0.71; P = .0004). The most common adverse events during maintenance were thrombocytopenia, anaemia, hypertension, dyspnoea and bacterial infections.</p><p><strong>Conclusion:</strong> In summary, maintenance therapy with carfilzomib and dexamethasone after salvage ASCT prolonged TTP with 8 months. The maintenance treatment was in general well-tolerated with manageable toxicity.</p>
dc.format.pagerange34
dc.format.pagerange44
dc.identifier.eissn1600-0609
dc.identifier.jour-issn0902-4441
dc.identifier.olddbid184577
dc.identifier.oldhandle10024/167671
dc.identifier.urihttps://www.utupub.fi/handle/11111/50581
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1111/ejh.13709
dc.identifier.urnURN:NBN:fi-fe2021120158499
dc.language.isoen
dc.okm.affiliatedauthorRemes, Kari
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWILEY
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1111/ejh.13709
dc.relation.ispartofjournalEuropean Journal of Haematology
dc.relation.issue1
dc.relation.volume108
dc.source.identifierhttps://www.utupub.fi/handle/10024/167671
dc.titleCarfilzomib and dexamethasone maintenance following salvage ASCT in multiple myeloma: A randomised phase 2 trial by the Nordic Myeloma Study Group
dc.year.issued2022

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