Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/7911
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dc.contributor.authorAleksandar Savićen_US
dc.contributor.authorDragomir Marisavljevićen_US
dc.contributor.authorVanja Kvrgićen_US
dc.contributor.authorNataša Stanisavljevićen_US
dc.date.accessioned2019-09-30T09:05:15Z-
dc.date.available2019-09-30T09:05:15Z-
dc.date.issued2014-01-01-
dc.identifier.issn15792en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/7911-
dc.description.abstractThe objective of this study is to externally validate the recently published Revised International Prognostic Scoring System (IPSS-R) for myelodysplastic syndrome (MDS) and compare it with the International Prognostic Scoring System (IPSS). We conducted a retrospective study of 173 adult MDS patients who had not received disease-altering treatment. Using the Cox hazard method, we found the IPSS-R to be a significant predictor of survival (p < 0.001, hazard ratio, HR = 1.82, 95% confidence interval, CI 1.57-2.12) and time to acute myeloid leukemia (AML; p < 0.001, HR = 2.05, 95% CI 1.55-2.70). The IPSS-R has greater prognostic power for survival and time to AML compared with the IPSS, given higher Somers' D values (0.41 vs. 0.39 and 0.55 vs. 0.53, respectively). Using the log-rank test, we found a significant difference when comparing IPSS-R groups (p < 0.02), with the exception of the high-risk versus very high-risk group comparison. The IPSS-R reclassified low-risk and intermediate-1 IPSS groups into four groups (log-rank, p < 0.001) and intermediate-2 and high-risk IPSS groups into three groups (log-rank, p < 0.04, excluding high-risk vs. very high-risk comparison). We conclude that the IPSS-R has significant prognostic utility for MDS patients. © 2013 S. Karger AG, Basel.en_US
dc.language.isoenen_US
dc.relation.ispartofActa Haematologicaen_US
dc.subjectPrognostic Scoring Systemen_US
dc.subjectmyelodysplastic syndromeen_US
dc.titleValidation of the revised international prognostic scoring system for patients with myelodysplastic syndromesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1159/000354840-
dc.identifier.pmid131-
dc.identifier.scopus2-s2.0-84901348957-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84901348957-
dc.description.versionPublisheden_US
dc.relation.lastpage238en_US
dc.relation.firstpage231en_US
dc.relation.issue4en_US
dc.relation.volume131en_US
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptMedicinski fakultet, Katedra za internu medicinu-
crisitem.author.parentorgMedicinski fakultet-
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