Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party

dc.contributor.authorScheid C
dc.contributor.authorde Wreede L
dc.contributor.authorvan Biezen A
dc.contributor.authorKoenecke C
dc.contributor.authorGohring G
dc.contributor.authorVolin L
dc.contributor.authorMaertens J
dc.contributor.authorFinke J
dc.contributor.authorPassweg J
dc.contributor.authorBeelen D
dc.contributor.authorCornelissen JJ
dc.contributor.authorItala-Remes M
dc.contributor.authorChevallier P
dc.contributor.authorRussell N
dc.contributor.authorPetersen E
dc.contributor.authorMilpied N
dc.contributor.authorEspiga CR
dc.contributor.authorPeniket A
dc.contributor.authorSierra J
dc.contributor.authorMufti G
dc.contributor.authorCrawley C
dc.contributor.authorVeelken JH
dc.contributor.authorLjungman P
dc.contributor.authorCahn JY
dc.contributor.authorAlessandrino EP
dc.contributor.authorde Witte T
dc.contributor.authorRobin M
dc.contributor.authorKroger N
dc.contributor.organizationfi=kliininen laitos|en=Department of Clinical Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.61334543354
dc.converis.publication-id27258050
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/27258050
dc.date.accessioned2022-10-28T14:14:24Z
dc.date.available2022-10-28T14:14:24Z
dc.description.abstractThe International Prognostic Scoring System has been revised (IPSS-R) to predict prognosis of patients with myelodysplastic syndromes at diagnosis. To validate the use of the IPSS-R assessed before transplant rather than at diagnosis we performed a retrospective analysis of the EBMT database. A total of 579 patients had sufficient information available to calculate IPSS-R at transplant. Median overall survival (OS) from transplant was significantly different according to IPSS-R: very low 23.6 months, low 55.0 months, intermediate 19.7 months, high 13.5 months, very high 7.8 months (P < 0.001). In a multivariate Cox model the following parameters were significant risk factors for OS: IPSS-R, graft source, age and prior treatment. Median relapse free survival also showed significant differences according to IPSS-R: very low: 23.6 months, low: 24.8 months, intermediate 10.6 months, high 7.9 months, very high 5.5 months (P < 0.001). Multivariate risk factors for relapse-free survival (RFS) were: IPSS-R, reduced intensity conditioning, graft source and prior treatment. A trend for an increased relapse incidence was noted for very high risk IPSS-R. We conclude that the IPSS-R at transplant is a useful prognostic score for predicting OS and RFS after transplantation, capturing both disease evolution and response to prior treatment before transplant.
dc.format.pagerange1525
dc.identifier.eissn1476-5365
dc.identifier.jour-issn0268-3369
dc.identifier.olddbid187106
dc.identifier.oldhandle10024/170200
dc.identifier.urihttps://www.utupub.fi/handle/11111/42399
dc.identifier.urlhttp://www.nature.com/articles/bmt2017171
dc.identifier.urnURN:NBN:fi-fe2021042717373
dc.language.isoen
dc.okm.affiliatedauthorItälä-Remes, Maija
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNATURE PUBLISHING GROUP
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/bmt.2017.171
dc.relation.ispartofjournalBone Marrow Transplantation
dc.relation.issue11
dc.relation.volume52
dc.source.identifierhttps://www.utupub.fi/handle/10024/170200
dc.titleValidation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
dc.year.issued2017

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