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dc.contributor.author문영철*
dc.date.accessioned2016-08-27T04:08:46Z-
dc.date.available2016-08-27T04:08:46Z-
dc.date.issued2015*
dc.identifier.issn0001-5792*
dc.identifier.issn1421-9662*
dc.identifier.otherOAK-15248*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/217378-
dc.description.abstractAzacitidine (AZA) is commonly used in patients with myelo-dysplastic syndrome (MDS). To determine the role of AZA before allogeneic stem cell transplantation (allo-SCT), we conducted a prospective study of AZA pre-treatment followed by allo-SCT in patients with higher-risk MDS. Twentyone patients who were scheduled for their third to sixth cycle of AZA pre-treatment followed by allo-SCT were enrolled. AZA pre-treatment was interrupted early in 3 patients (14.3%) because of leukaemic transformation or death. The overall response rate to AZA pre-treatment was 57.1%. There were 2 cases of complete remission, 1 case of partial remission, and 9 cases of haematologic improvement. Fourteen patients (66.7%) received the planned allo-SCT and 5 patients were alive at the last follow-up. Three-year progression-free survival (PFS) and 3-year overall survival (OS) in the 14 patients who received allo-SCT were 30.0% (95% CI 3.3-56.7) and 42.9% (95% CI 17.1-68.7), respectively. PFS and OS were not influenced by response to AZA pre-treatment (p > 0.05). In this study, AZA had a role as a bridge therapy to prevent leukaemic transformation prior to selection of a donor for allo-SCT and showed low toxicity. It may be considered in patients with higher-risk MDS. (C) 2015 S. Karger AG, Basel*
dc.languageEnglish*
dc.publisherKARGER*
dc.subjectMyelodysplastic syndrome*
dc.subjectAzacitidine*
dc.subjectAllogeneic stem cell transplantation*
dc.titleAzacitidine Pre-Treatment Followed by Reduced-Intensity Stem Cell Transplantation in Patients with Higher-Risk Myelodysplastic Syndrome*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume134*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage40*
dc.relation.lastpage48*
dc.relation.journaltitleACTA HAEMATOLOGICA*
dc.identifier.doi10.1159/000368711*
dc.identifier.wosidWOS:000356978200007*
dc.author.googleAhn, Jae-Sook*
dc.author.googleKim, Yeo-Kyeoung*
dc.author.googleMin, Yoo Hong*
dc.author.googleCheong, June-Won*
dc.author.googleJang, Jun Ho*
dc.author.googleJung, Chul Won*
dc.author.googleKim, In Ho*
dc.author.googleYoon, Hwi-Joong*
dc.author.googleLee, Hong Ghi*
dc.author.googleSohn, Sang Kyun*
dc.author.googleMoon, Joon Ho*
dc.author.googleKim, Hawk*
dc.author.googleKim, Yoo-Jin*
dc.author.googleWon, Jong-Ho*
dc.author.googleChung, Joo-Seop*
dc.author.googleMun, Yeung Chul*
dc.author.googleLee, Je-Hwan*
dc.author.googleKim, Hyeoung-Joon|Korean Soc Hematology AML MDS Work*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20240422115947*
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의과대학 > 의학과 > Journal papers
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