Ixazomib, Lenalidomide, and Dexamethasone (IRD) Treatment with Cytogenetic Risk-Based Maintenance in Transplant-Eligible Myeloma: A Phase 2 Multicenter Study by the Nordic Myeloma Study Group

dc.contributor.authorPartanen Anu
dc.contributor.authorWaage Anders
dc.contributor.authorPeceliunas Valdas
dc.contributor.authorSchjesvold Fredrik
dc.contributor.authorAnttila Pekka
dc.contributor.authorSäily Marjaana
dc.contributor.authorUttervall Katarina
dc.contributor.authorPutkonen Mervi
dc.contributor.authorCarlson Kristina
dc.contributor.authorHaukas Einar
dc.contributor.authorSankelo Marja
dc.contributor.authorSzatkowski Damian
dc.contributor.authorHansson Markus
dc.contributor.authorMarttila Anu
dc.contributor.authorSvensson Ronald
dc.contributor.authorAxelsson Per
dc.contributor.authorLauri Birgitta
dc.contributor.authorMikkola Maija
dc.contributor.authorKarlsson Conny
dc.contributor.authorAbelsson Johanna
dc.contributor.authorAhlstrand Erik
dc.contributor.authorSikiö Anu
dc.contributor.authorKlimkowska Monika
dc.contributor.authorMatuzeviciene Reda
dc.contributor.authorFenstad Mona Hoysaeter
dc.contributor.authorIlveskero Sorella
dc.contributor.authorPelliniemi Tarja-Terttu
dc.contributor.authorNahi Hareth
dc.contributor.authorSilvennoinen Raija
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.converis.publication-id393372850
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/393372850
dc.date.accessioned2025-08-27T23:40:17Z
dc.date.available2025-08-27T23:40:17Z
dc.description.abstract<p>Scarce data exist on double maintenance in transplant-eligible high-risk (HR) newly diagnosed multiple myeloma (NDMM) patients. This prospective phase 2 study enrolled 120 transplant-eligible NDMM patients. The treatment consisted of four cycles of ixazomib-lenalidomide-dexamethasone (IRD) induction plus autologous stem cell transplantation followed by IRD consolidation and cytogenetic risk-based maintenance therapy with lenalidomide + ixazomib (IR) for HR patients and lenalidomide (R) alone for NHR patients. The main endpoint of the study was undetectable minimal residual disease (MRD) with sensitivity of <10<sup>-5</sup> by flow cytometry at any time, and other endpoints were progression-free survival (PFS) and overall survival (OS). We present the preplanned analysis after the last patient has been two years on maintenance. At any time during protocol treatment, 28% (34/120) had MRD < 10<sup>-5</sup> at least once. At two years on maintenance, 66% of the patients in the HR group and 76% in the NHR group were progression-free (<em>p</em> = 0.395) and 36% (43/120) were CR or better, of which 42% (18/43) had undetectable flow MRD <10<sup>-5</sup>. Altogether 95% of the patients with sustained MRD <10<sup>-5</sup>, 82% of the patients who turned MRD-positive, and 61% of those with positive MRD had no disease progression at two years on maintenance (<em>p</em> < 0.001). To conclude, prolonged maintenance with all-oral ixazomib plus lenalidomide might improve PFS in HR patients.<br></p>
dc.identifier.eissn2072-6694
dc.identifier.jour-issn2072-6694
dc.identifier.olddbid204396
dc.identifier.oldhandle10024/187423
dc.identifier.urihttps://www.utupub.fi/handle/11111/52624
dc.identifier.urlhttps://doi.org./10.3390/cancers16051024
dc.identifier.urnURN:NBN:fi-fe2025082786423
dc.language.isoen
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumberARTN 1024
dc.relation.doi10.3390/cancers16051024
dc.relation.ispartofjournalCancers
dc.relation.issue5
dc.relation.volume16
dc.source.identifierhttps://www.utupub.fi/handle/10024/187423
dc.titleIxazomib, Lenalidomide, and Dexamethasone (IRD) Treatment with Cytogenetic Risk-Based Maintenance in Transplant-Eligible Myeloma: A Phase 2 Multicenter Study by the Nordic Myeloma Study Group
dc.year.issued2024

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