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dc.contributor.author엄지은-
dc.date.accessioned2018-04-03T00:57:39Z-
dc.date.available2018-04-03T00:57:39Z-
dc.date.issued2014-06-
dc.identifier.citationBONE MARROW TRANSPLANTATION, 49(9),p.1162-1169en_US
dc.identifier.issn0268-3369-
dc.identifier.issn1476-5365-
dc.identifier.urihttp://www.nature.com/articles/bmt2014131-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/55407-
dc.description.abstractGraft failure is one of the major barriers to the success of allogeneic hematopoietic cell transplantation (HCT) in myelofibrosis (MF). We report our institutional experience with 27 MF patients who underwent HCT using fludarabine-, intravenous BU- and low-dose total body irradiation (FBT)-based reduced-intensity (n = 20) or full-intensity (n = 7) conditioning regimens. Eight patients had prior exposure to JAK1/2 inhibitor therapy; six patients received JAK1/2 inhibitors leading on to HCT and two patients received transplant at the failure of JAK1/2 inhibitor therapy. No adverse impact of JAK1/2 inhibitor therapy was observed on early post-transplant outcomes. All evaluable patients had neutrophil recovery, and no primary graft failure was observed. Cumulative incidence of grades II-IV acute GVHD at day 100 was 48% (95% confidence interval (CI), 29-67%) and chronic GVHD at 2 years was 66% (95% CI, 49-84%). Cumulative incidences of nonrelapse mortality (NRM), relapse and probability of OS at 2 years were: 43% (95% CI, 12-74%), 10% (95% CI, 0-39%) and 56% (95% CI, 28-77%), respectively. FBT-based conditioning regimen has a favorable impact on engraftment; however, further efforts are required to reduce NRM.en_US
dc.description.sponsorshipVG received grant for research studies from Incyte and Novartis through his institution, and has served as a consultant on advisory board for Incyte and Novartis. The remaining authors declare no conflict of interest.en_US
dc.language.isoenen_US
dc.publisherNATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLANDen_US
dc.titleAllogeneic hematopoietic cell transplantation for myelofibrosis using fludarabine-, intravenous busulfan- and low-dose TBI-based conditioningen_US
dc.typeArticleen_US
dc.relation.no9-
dc.relation.volume49-
dc.identifier.doi10.1038/bmt.2014.131-
dc.relation.page1162-1169-
dc.relation.journalBONE MARROW TRANSPLANTATION-
dc.contributor.googleauthorShanavas, M.-
dc.contributor.googleauthorMessner, H. A.-
dc.contributor.googleauthorAtenafu, E. G.-
dc.contributor.googleauthorKim, D. H.-
dc.contributor.googleauthorKuruvilla, J.-
dc.contributor.googleauthorLipton, J. H.-
dc.contributor.googleauthorUhm, J.-
dc.contributor.googleauthorSeftel, M-
dc.contributor.googleauthorAlam, N.-
dc.contributor.googleauthorGupta, V.-
dc.relation.code2014026371-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidjieunuhm-
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COLLEGE OF MEDICINE[S](의과대학) > ETC
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