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dc.contributor.authorPanopoulou, A
dc.contributor.authorEasdale, S
dc.contributor.authorEthell, M
dc.contributor.authorNicholson, E
dc.contributor.authorPotter, M
dc.contributor.authorGiotas, A
dc.contributor.authorWoods, H
dc.contributor.authorThornton, T
dc.contributor.authorPawlyn, C
dc.contributor.authorBoyd, KD
dc.contributor.authorKaiser, MF
dc.coverage.spatialUnited States
dc.date.accessioned2023-02-21T13:21:05Z
dc.date.available2023-02-21T13:21:05Z
dc.date.issued2023-02-01
dc.identifier.citationHemaSphere, 2023, 7 (2), pp. e831 -
dc.identifier.issn2572-9241
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5692
dc.identifier.eissn2572-9241
dc.identifier.eissn2572-9241
dc.identifier.doi10.1097/HS9.0000000000000831
dc.description.abstractRefined prediction of early relapse following standard-of-care (SoC) autologous stem cell transplant (ASCT) in newly diagnosed multiple myeloma (NDMM) could inform real-world risk-stratified post-ASCT strategies. We investigated the impact of double hit genetics (≥2 adverse markers: t(4;14), t(14;16), t(14;20), gain(1q), del(17p)) on outcome in 139 NDMM patients who underwent SoC ASCT between January 2014 and October 2019 at our center. Double hit genetics were associated with a significantly shortened progression-free survival (hazard ratio [HR] = 4.27, P < 0.001) and overall survival (HR = 4.01, P = 0.03), and characterized most early relapses. Our results support the real-world utility of extended genetic profiling for improved risk prediction in NDMM.
dc.formatElectronic-eCollection
dc.format.extente831 -
dc.languageeng
dc.language.isoeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relation.ispartofHemaSphere
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleImpact of Ultra High-risk Genetics on Real-world Outcomes of Transplant-eligible Multiple Myeloma Patients.
dc.typeJournal Article
dcterms.dateAccepted2022-12-19
dc.date.updated2023-02-21T11:34:08Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1097/HS9.0000000000000831
rioxxterms.licenseref.startdate2023-02-01
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36751511
pubs.issue2
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Myeloma Molecular Therapy
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1097/hs9.0000000000000831
pubs.volume7
icr.researchteamMyeloma Molecular Therapy
dc.contributor.icrauthorPawlyn, Charlotte
dc.contributor.icrauthorKaiser, Martin
icr.provenanceDeposited by Dr Martin Kaiser on 2023-02-21. Deposit type is initial. No. of files: 1. Files: Impact of Ultra High-risk Genetics on Real-world Outcomes of Transplant-eligible Multiple Myeloma Patients.pdf


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