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.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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