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Improved Outcome of a Reduced Toxicity-Fludarabine, Cyclophosphamide, plus Antithymocyte Globulin Conditioning Regimen for Unrelated Donor Transplantation in Severe Aplastic Anemia: Comparison of 2 Multicenter Prospective Studies

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dc.contributor.authorKang, Hyoung Jin-
dc.contributor.authorHong, Kyung Taek-
dc.contributor.authorLee, Ji Won-
dc.contributor.authorKim, Hyery-
dc.contributor.authorPark, Kyung Duk-
dc.contributor.authorShin, Hee Young-
dc.contributor.authorLee, Soo Hyun-
dc.contributor.authorYoo, Keon Hee-
dc.contributor.authorSung, Ki Woong-
dc.contributor.authorKoo, Hong Hoe-
dc.contributor.authorLee, Jae Wook-
dc.contributor.authorChung, Nak Gyun-
dc.contributor.authorCho, Bin-
dc.contributor.authorKim, Hack Ki-
dc.contributor.authorKoh, Kyung Nam-
dc.contributor.authorIm, Ho Joon-
dc.contributor.authorSeo, Jong Jin-
dc.contributor.authorJung, Hyun Joo-
dc.contributor.authorPark, Jun Eun-
dc.contributor.authorLee, Young Ho-
dc.contributor.authorLim, Young Tak-
dc.contributor.authorLim, Yeon Jung-
dc.contributor.authorKim, Sun Young-
dc.contributor.authorYoo, Eun Sun-
dc.contributor.authorRyu, Kyung Ha-
dc.contributor.authorLee, Jae Hee-
dc.contributor.authorPark, Jeong-A-
dc.contributor.authorPark, Sang Kyu-
dc.contributor.authorAhn, Hyo Seop-
dc.date.accessioned2023-03-08T16:59:19Z-
dc.date.available2023-03-08T16:59:19Z-
dc.date.issued2016-08-
dc.identifier.issn1083-8791-
dc.identifier.issn1523-6536-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/64189-
dc.description.abstractHematopoietic stem cell transplantation (HSCT) is a curative therapy for severe aplastic anemia (SAA); however, the optimal conditioning regimen for HSCT with an unrelated donor has not yet been defined. A previous study using a fludarabine (FLU), cyclophosphamide (Cy), and antithymocyte globulin (ATG) conditioning regimen (study A: 50 mg/kg Cy once daily i.v. on days -9, -8, -7, and -6; 30 mg/m(2) FLU once daily i.v. on days -5, -4, -3, and -2; and 2.5 mg/kg of ATG once daily i.v. on days -3, -2, and -1) demonstrated successful engraftment (100%) but had a high treatment-related mortality rate (32.1%). Therefore, given that Cy is more toxic than FLU, we performed a new phase II prospective study with a reduced-toxicity regimen (study B: 60 mg/kg Cy once daily i.v. on days -8 and -7; 40 mg/m(2) FLU once daily i.v. on days -6, -5, -4, -3, and -2; and 2.5 mg/kg ATG once daily i.v. on 3 days). Fifty-seven patients were enrolled in studies A (n = 28) and B (n = 29), and donor type hematologic recovery was achieved in all patients in both studies. The overall survival (OS) and event-free survival (EFS) rates of patients in study B was markedly improved compared with those in study A (OS: 96.7% versus 67.9%, respectively, P =.004; EFS: 93.3% versus 64.3%, respectively, P =.008). These data show that a reduced-toxicity conditioning regimen with FLU, Cy, and ATG may be an optimal regimen for SAA patients receiving unrelated donor HSCT. (C) 2016 American Society for Blood and Marrow Transplantation.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE INC-
dc.titleImproved Outcome of a Reduced Toxicity-Fludarabine, Cyclophosphamide, plus Antithymocyte Globulin Conditioning Regimen for Unrelated Donor Transplantation in Severe Aplastic Anemia: Comparison of 2 Multicenter Prospective Studies-
dc.typeArticle-
dc.identifier.doi10.1016/j.bbmt.2016.04.003-
dc.identifier.bibliographicCitationBIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, v.22, no.8, pp 1455 - 1459-
dc.description.isOpenAccessN-
dc.identifier.wosid000380417400017-
dc.identifier.scopusid2-s2.0-84976516781-
dc.citation.endPage1459-
dc.citation.number8-
dc.citation.startPage1455-
dc.citation.titleBIOLOGY OF BLOOD AND MARROW TRANSPLANTATION-
dc.citation.volume22-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorSevere aplastic anemia-
dc.subject.keywordAuthorUnrelated donor-
dc.subject.keywordAuthorFludarabine-
dc.subject.keywordAuthorCyclophosphamide-
dc.subject.keywordAuthorThymoglobulin-
dc.subject.keywordAuthorAntithymocyte globulin (ATG)-
dc.subject.keywordPlusSTEM-CELL TRANSPLANTATION-
dc.subject.keywordPlusVERSUS-HOST-DISEASE-
dc.subject.keywordPlusMARROW TRANSPLANTATION-
dc.subject.keywordPlusIMMUNOSUPPRESSIVE THERAPY-
dc.subject.keywordPlusCHILDREN-
dc.subject.keywordPlusFAILURE-
dc.subject.keywordPlusTHYMOGLOBULIN-
dc.subject.keywordPlusIRRADIATION-
dc.subject.keywordPlusATG-
dc.relation.journalResearchAreaHematology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaTransplantation-
dc.relation.journalWebOfScienceCategoryHematology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryTransplantation-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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