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dc.contributor.authorD'Agostino, M
dc.contributor.authorCairns, DA
dc.contributor.authorLahuerta, JJ
dc.contributor.authorWester, R
dc.contributor.authorBertsch, U
dc.contributor.authorWaage, A
dc.contributor.authorZamagni, E
dc.contributor.authorMateos, M-V
dc.contributor.authorDall'Olio, D
dc.contributor.authorvan de Donk, NWCJ
dc.contributor.authorJackson, G
dc.contributor.authorRocchi, S
dc.contributor.authorSalwender, H
dc.contributor.authorBladé Creixenti, J
dc.contributor.authorvan der Holt, B
dc.contributor.authorCastellani, G
dc.contributor.authorBonello, F
dc.contributor.authorCapra, A
dc.contributor.authorMai, EK
dc.contributor.authorDürig, J
dc.contributor.authorGay, F
dc.contributor.authorZweegman, S
dc.contributor.authorCavo, M
dc.contributor.authorKaiser, MF
dc.contributor.authorGoldschmidt, H
dc.contributor.authorHernández Rivas, JM
dc.contributor.authorLarocca, A
dc.contributor.authorCook, G
dc.contributor.authorSan-Miguel, JF
dc.contributor.authorBoccadoro, M
dc.contributor.authorSonneveld, P
dc.coverage.spatialUnited States
dc.date.accessioned2022-08-12T14:53:32Z
dc.date.available2022-08-12T14:53:32Z
dc.date.issued2022-10-10
dc.identifier.citationJournal of Clinical Oncology, 2022, pp. JCO2102614 -
dc.identifier.issn0732-183X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5262
dc.identifier.eissn1527-7755
dc.identifier.eissn1527-7755
dc.identifier.doi10.1200/JCO.21.02614
dc.description.abstractPURPOSE: Patients with newly diagnosed multiple myeloma (NDMM) show heterogeneous outcomes, and approximately 60% of them are at intermediate-risk according to the Revised International Staging system (R-ISS), the standard-of-care risk stratification model. Moreover, chromosome 1q gain/amplification (1q+) recently proved to be a poor prognostic factor. In this study, we revised the R-ISS by analyzing the additive value of each single risk feature, including 1q+. PATIENTS AND METHODS: The European Myeloma Network, within the HARMONY project, collected individual data from 10,843 patients with NDMM enrolled in 16 clinical trials. An additive scoring system on the basis of top features predicting progression-free survival (PFS) and overall survival (OS) was developed and validated. RESULTS: In the training set (N = 7,072), at a median follow-up of 75 months, ISS, del(17p), lactate dehydrogenase, t(4;14), and 1q+ had the highest impact on PFS and OS. These variables were all simultaneously present in 2,226 patients. A value was assigned to each risk feature according to their OS impact (ISS-III 1.5, ISS-II 1, del(17p) 1, high lactate dehydrogenase 1, and 1q+ 0.5 points). Patients were stratified into four risk groups according to the total additive score: low (Second Revision of the International Staging System [R2-ISS]-I, 19.2%, 0 points), low-intermediate (II, 30.8%, 0.5-1 points), intermediate-high (III, 41.2%, 1.5-2.5 points), high (IV, 8.8%, 3-5 points). Median OS was not reached versus 109.2 versus 68.5 versus 37.9 months, and median PFS was 68 versus 45.5 versus 30.2 versus 19.9 months, respectively. The score was validated in an independent validation set (N = 3,771, of whom 1,214 were with complete data to calculate R2-ISS) maintaining its prognostic value. CONCLUSION: The R2-ISS is a simple prognostic staging system allowing a better stratification of patients with intermediate-risk NDMM. The additive nature of this score fosters its future implementation with new prognostic variables.
dc.formatPrint-Electronic
dc.format.extentJCO2102614 -
dc.languageeng
dc.language.isoeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relation.ispartofJournal of Clinical Oncology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleSecond Revision of the International Staging System (R2-ISS) for Overall Survival in Multiple Myeloma: A European Myeloma Network (EMN) Report Within the HARMONY Project.
dc.typeJournal Article
dcterms.dateAccepted2022-04-08
dc.date.updated2022-08-12T14:52:37Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1200/JCO.21.02614
rioxxterms.licenseref.startdate2022-05-23
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35605179
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
icr.researchteamMyeloma Molecular Therapy
dc.contributor.icrauthorKaiser, Martin
icr.provenanceDeposited by Mr Arek Surman on 2022-08-12. Deposit type is initial. No. of files: 1. Files: jco.21.02614.pdf


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