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dc.contributor.authorDavies, FE
dc.contributor.authorPawlyn, C
dc.contributor.authorUsmani, SZ
dc.contributor.authorSan-Miguel, JF
dc.contributor.authorEinsele, H
dc.contributor.authorBoyle, EM
dc.contributor.authorCorre, J
dc.contributor.authorAuclair, D
dc.contributor.authorCho, HJ
dc.contributor.authorLonial, S
dc.contributor.authorSonneveld, P
dc.contributor.authorStewart, AK
dc.contributor.authorBergsagel, PL
dc.contributor.authorKaiser, MF
dc.contributor.authorWeisel, K
dc.contributor.authorKeats, JJ
dc.contributor.authorMikhael, JR
dc.contributor.authorMorgan, KE
dc.contributor.authorGhobrial, IM
dc.contributor.authorOrlowski, RZ
dc.contributor.authorLandgren, CO
dc.contributor.authorGay, F
dc.contributor.authorCaers, J
dc.contributor.authorChng, WJ
dc.contributor.authorChari, A
dc.contributor.authorWalker, BA
dc.contributor.authorKumar, SK
dc.contributor.authorCosta, LJ
dc.contributor.authorAnderson, KC
dc.contributor.authorMorgan, GJ
dc.coverage.spatialUnited States
dc.date.accessioned2022-08-23T11:34:19Z
dc.date.available2022-08-23T11:34:19Z
dc.date.issued2022-07-06
dc.identifier699310
dc.identifier.citationBlood Cancer Discov, 2022, 3 (4), pp. 273 - 284
dc.identifier.issn2643-3230
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5314
dc.identifier.eissn2643-3249
dc.identifier.eissn2643-3249
dc.identifier.doi10.1158/2643-3230.BCD-21-0205
dc.description.abstractThe multiple myeloma treatment landscape has changed dramatically. This change, paralleled by an increase in scientific knowledge, has resulted in significant improvement in survival. However, heterogeneity remains in clinical outcomes, with a proportion of patients not benefiting from current approaches and continuing to have a poor prognosis. A significant proportion of the variability in outcome can be predicted on the basis of clinical and biochemical parameters and tumor-acquired genetic variants, allowing for risk stratification and a more personalized approach to therapy. This article discusses the principles that can enable the rational and effective development of therapeutic approaches for high-risk multiple myeloma.
dc.formatPrint
dc.format.extent273 - 284
dc.languageeng
dc.language.isoeng
dc.publisherAMER ASSOC CANCER RESEARCH
dc.relation.ispartofBlood Cancer Discov
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectHumans
dc.subjectMultiple Myeloma
dc.subjectPrognosis
dc.titlePerspectives on the Risk-Stratified Treatment of Multiple Myeloma.
dc.typeJournal Article
dcterms.dateAccepted2022-07-01
dc.date.updated2022-08-23T11:33:20Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1158/2643-3230.BCD-21-0205
rioxxterms.licenseref.startdate2022-07-06
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35653112
pubs.issue4
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/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Myeloma Biology and Therapeutics
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Myeloma Molecular Therapy
pubs.organisational-group/ICR/Students/PhD and MPhil/13/14 Starting Cohort
pubs.publication-statusPublished
pubs.volume3
icr.researchteamMyeloma Biol Therap
icr.researchteamMyeloma Molecular Therapy
dc.contributor.icrauthorPawlyn, Charlotte
dc.contributor.icrauthorKaiser, Martin
icr.provenanceDeposited by Mr Arek Surman on 2022-08-23. Deposit type is initial. No. of files: 1. Files: bcd-21-0205.pdf


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/