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Busulfan-containing conditioning regimens are optimal preparative regimens for autologous stem cell transplant in patients with diffuse large B-cell lymphoma

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dc.contributor.authorShin, Ho-Jin-
dc.contributor.authorLee, Won-Sik-
dc.contributor.authorLee, Ho-Seop-
dc.contributor.authorKim, Hawk-
dc.contributor.authorLee, Gyeong-Won-
dc.contributor.authorSong, Moo-Kon-
dc.contributor.authorKim, Jin Seok-
dc.contributor.authorYhim, Ho-Young-
dc.contributor.authorChung, Joo Seop-
dc.date.accessioned2022-12-26T22:50:23Z-
dc.date.available2022-12-26T22:50:23Z-
dc.date.issued2014-11-
dc.identifier.issn1042-8194-
dc.identifier.issn1029-2403-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18670-
dc.description.abstractWe retrospectively examined the outcomes of 56 patients with diffuse large B-cell lymphoma (DLBCL) who underwent autologous stem cell transplant (ASCT) with BEAM/BEAC (carmustine, etoposide, cytarabine, melphalan/cyclophosphamide) or busulfan (Bu)-containing conditioning regimens. The Bu group had lower disease-related mortality and more frequent achievement of complete remission (CR) after ASCT from partial remission (PR) or refractory status before ASCT compared with the BEAM/BEAC group. The estimated 2-year EFS (59.3% vs. 15.0%) and overall survival (OS) (70.2% vs. 42.0%) in pre-ASCT rituximab-exposed patients with DLBCL were higher in the Bu group. In patients with high-risk DLBCL exposed to rituximab with first remission, the Bu group had better EFS (p = 0.004) and OS (p = 0.053) rates, while survival rates for relapsed/refractory patients did not differ between groups. Bu regimens are highly effective for preparing patients with DLBCL with previous exposure to rituximab for ASCT, especially in high-risk patients who achieved a first remission.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherTAYLOR & FRANCIS LTD-
dc.titleBusulfan-containing conditioning regimens are optimal preparative regimens for autologous stem cell transplant in patients with diffuse large B-cell lymphoma-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.3109/10428194.2014.882504-
dc.identifier.scopusid2-s2.0-84912111705-
dc.identifier.wosid000344339000013-
dc.identifier.bibliographicCitationLEUKEMIA & LYMPHOMA, v.55, no.11, pp 2490 - 2496-
dc.citation.titleLEUKEMIA & LYMPHOMA-
dc.citation.volume55-
dc.citation.number11-
dc.citation.startPage2490-
dc.citation.endPage2496-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaHematology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryHematology-
dc.subject.keywordPlusNON-HODGKINS-LYMPHOMA-
dc.subject.keywordPlusBONE-MARROW-TRANSPLANTATION-
dc.subject.keywordPlusHIGH-DOSE CHEMOTHERAPY-
dc.subject.keywordPlusINTRAVENOUS BUSULFAN-
dc.subject.keywordPlusCYCLOPHOSPHAMIDE-
dc.subject.keywordPlusETOPOSIDE-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusOUTCOMES-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusBEAC-
dc.subject.keywordAuthorBusulfan-
dc.subject.keywordAuthorBEAM regimen-
dc.subject.keywordAuthorhematopoietic stem cell transplant-
dc.subject.keywordAuthorlymphoma-
dc.subject.keywordAuthorlarge B-cell-
dc.subject.keywordAuthordiffuse-
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