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Validation of the revised international prognostic scoring system (IPSS-R) in patients with lower-risk myelodysplastic syndromes: a report from the prospective European LeukaemiaNet MDS (EUMDS) registry

dc.contributor.authorSwart, L. de
dc.contributor.authorSmith, Alex
dc.contributor.authorJohnston, T. W.
dc.contributor.authorHaase, D.
dc.contributor.authorDroste, J.
dc.contributor.authorFenaux, P.
dc.contributor.authorSymeonidis, Argiris
dc.contributor.authorSanz, Guillermo
dc.contributor.authorHellström Lindberg, E.
dc.contributor.authorLuño Fernández, Elisa 
dc.date.accessioned2015-05-21T11:21:25Z
dc.date.available2015-05-21T11:21:25Z
dc.date.issued2015
dc.identifier.citationBritish Journal of Haematology, 170(3), p. 372–383 (2015); doi:10.1111/bjh.13450
dc.identifier.issn0007-1048
dc.identifier.issn1365-2141
dc.identifier.urihttp://hdl.handle.net/10651/30923
dc.description.abstractBaseline characteristics, disease-management and outcome of 1000 lower-risk myelodysplastic syndrome (MDS) patients within the European LeukaemiaNet MDS (EUMDS) Registry are described in conjunction with the validation of the revised International Prognostic Scoring System (IPSS-R). The EUMDS registry confirmed established prognostic factors, such as age, gender and World Health Organization 2001 classification. Low quality of life (EQ-5D visual analogue scale score) was significantly associated with reduced survival. A high co-morbidity index predicted poor outcome in univariate analyses. The IPSS-R identified a large group of 247 patients with Low (43%) and Very low (23%) risk score within the IPSS intermediate-1 patients. The IPSS-R also identified 32 High or Very high risk patients within the IPSS intermediate-1 patients. IPSS-R was superior to the IPSS for predicting both disease progression and survival. Seventy percent of patients received MDS-specific treatment or supportive care, including red blood cell transfusions (51%), haematopoietic growth factors (58%) and iron chelation therapy (8%), within 2 years of diagnosis; while 30% of the patients only required active monitoring. The IPSS-R proved its utility as a more refined risk stratification tool for the identification of patients with a very good or poor prognosis and in this lower-risk MDS population.spa
dc.description.statementofresponsibilityde Swart, L., Smith, A., Johnston, T.W., Haase, D., Droste, J., Fenaux, P., Symeonidis, A., Sanz, G., Hellström-Lindberg, E., Cermák, J., Germing, U., Stauder, R., Georgescu, O., MacKenzie, M., Malcovati, L., Holm, M.S., Almeida, A.M., Mądry, K., Slama, B., Guerci-Bresler, A., Sanhes, L., Beyne-Rauzy, O., Luño, E., Bowen, D., de Witte, T.
dc.language.isoengspa
dc.publisherWiley
dc.relation.ispartofBritish Journal of Haematologyspa
dc.rights© 2015 John Wiley & Sons Ltd
dc.titleValidation of the revised international prognostic scoring system (IPSS-R) in patients with lower-risk myelodysplastic syndromes: a report from the prospective European LeukaemiaNet MDS (EUMDS) registryspa
dc.typejournal article
dc.identifier.doi10.1111/bjh.13450
dc.relation.publisherversionhttp://dx.doi.org/10.1111/bjh.13450


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