RVD induction and autologous stem cell transplantation followed by lenalidomide maintenance in newly diagnosed multiple myeloma: a phase 2 study of the Finnish Myeloma Group

dc.contributor.authorSini Luoma
dc.contributor.authorPekka Anttila
dc.contributor.authorMarjaana Säily
dc.contributor.authorTuija Lundan
dc.contributor.authorJouni Heiskanen
dc.contributor.authorTimo Siitonen
dc.contributor.authorSakari Kakko
dc.contributor.authorMervi Putkonen
dc.contributor.authorHanna Ollikainen
dc.contributor.authorVenla Terävä
dc.contributor.authorMarja Sankelo
dc.contributor.authorAnu Partanen
dc.contributor.authorKirsi Launonen
dc.contributor.authorAnu Räsänen
dc.contributor.authorAnu Sikiö
dc.contributor.authorMerja Suominen
dc.contributor.authorPiotr Bazia
dc.contributor.authorKristiina Kananen
dc.contributor.authorJuha Lievonen
dc.contributor.authorTuomas Selander
dc.contributor.authorTarja-Terttu Pelliniemi
dc.contributor.authorSorella Ilveskero
dc.contributor.authorVirva Huotari
dc.contributor.authorPentti Mäntymaa
dc.contributor.authorAnri Tienhaara
dc.contributor.authorEsa Jantunen
dc.contributor.authorRaija Silvennoinen
dc.contributor.organizationfi=kliininen kemia|en=Clinical Chemistry|
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code2607318
dc.converis.publication-id45159108
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/45159108
dc.date.accessioned2022-10-27T12:16:02Z
dc.date.available2022-10-27T12:16:02Z
dc.description.abstractAutologous stem cell transplantation (ASCT) combined with novel agents is the standard treatment for transplant-eligible, newly diagnosed myeloma (NDMM) patients. Lenalidomide is approved for maintenance after ASCT until progression, although the optimal duration of maintenance is unknown. In this trial, 80 patients with NDMM received three cycles of lenalidomide, bortezomib, and dexamethasone followed by ASCT and lenalidomide maintenance until progression or toxicity. The primary endpoint was the proportion of flow-negative patients. Molecular response was assessed if patients were flow-negative or in stringent complete response (sCR). By intention to treat, the overall response rate was 89%. Neither median progression-free survival nor overall survival (OS) has been reached. The OS at 3 years was 83%. Flow-negativity was reached in 53% and PCR-negativity in 28% of the patients. With a median follow-up of 27 months, 29 (36%) patients are still on lenalidomide and 66% of them have sustained flow-negativity. Lenalidomide maintenance phase was reached in 8/16 high-risk patients but seven of them have progressed after a median of only 6 months. In low- or standard-risk patients, the outcome was promising, but high-risk patients need more effective treatment approach. Flow-negativity with the conventional flow was an independent predictor for longer PFS.
dc.format.pagerange2781
dc.format.pagerange2792
dc.identifier.eissn1432-0584
dc.identifier.jour-issn0939-5555
dc.identifier.olddbid174320
dc.identifier.oldhandle10024/157414
dc.identifier.urihttps://www.utupub.fi/handle/11111/34130
dc.identifier.urnURN:NBN:fi-fe2021042822870
dc.language.isoen
dc.okm.affiliatedauthorPutkonen, Mervi
dc.okm.affiliatedauthorDataimport, Kliininen kemia
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGER
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s00277-019-03815-7
dc.relation.ispartofjournalAnnals of Hematology
dc.relation.issue12
dc.relation.volume98
dc.source.identifierhttps://www.utupub.fi/handle/10024/157414
dc.titleRVD induction and autologous stem cell transplantation followed by lenalidomide maintenance in newly diagnosed multiple myeloma: a phase 2 study of the Finnish Myeloma Group
dc.year.issued2019

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