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dc.contributor.author문영철*
dc.date.accessioned2016-08-29T12:08:08Z-
dc.date.available2016-08-29T12:08:08Z-
dc.date.issued2015*
dc.identifier.issn0902-4441*
dc.identifier.otherOAK-14982*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/230586-
dc.description.abstractThis study aimed to determine the objective response, toxicity, and clinical outcome of weekly rituximab consolidation after four cycles of R-CHOP21 in very elderly patients with DLBCL. A prospective, multi-institutional phase II trial was conducted on patients with previously untreated CD20+ DLBCL who were older than 70 yr. Patients were treated with four cycles of R-CHOP21 followed by weekly consolidation with rituximab (375mg/m2, four times infusion) (NCT01181999). We also compared the clinical outcomes with an historical case-matched control group treated conventionally with six cycles of R-CHOP21. A total of 51 patients with newly diagnosed DLBCL were enrolled at 15 institutes between June 2010 and September 2013. The median age was 76 yr (range: 70-89). Forty-one of the 51 patients completed the planned rituximab consolidation (R-consolidation). The overall response rate was 78.4%, comprising 74.5% with a complete response and 3.9% with a partial response. After a median follow-up of 20.3 months, 2-yr progression-free survival and overall survival were 63.9% and 68.7%, respectively. No serious toxicities were reported during rituximab consolidation. Weekly rituximab consolidation following four cycles of R-CHOP21 resulted in an acceptable response with high tolerability and could be a good compromise between efficacy and safety for elderly patients with DLBCL. © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.*
dc.languageEnglish*
dc.publisherBlackwell Publishing Ltd*
dc.subjectDiffuse large B-cell lymphoma*
dc.subjectElderly*
dc.subjectRituximab consolidation*
dc.titleWeekly rituximab consolidation following four cycles of R-CHOP induction chemotherapy in very elderly patients with diffuse large B-cell lymphoma: Consortium for improving survival of lymphoma study (CISL)*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume94*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage504*
dc.relation.lastpage510*
dc.relation.journaltitleEuropean Journal of Haematology*
dc.identifier.doi10.1111/ejh.12459*
dc.identifier.wosidWOS:000354370400006*
dc.identifier.scopusid2-s2.0-84929070416*
dc.author.googleJung S.-H.*
dc.author.googleLee J.-J.*
dc.author.googleKim W.S.*
dc.author.googleLee W.-S.*
dc.author.googleDo Y.R.*
dc.author.googleOh S.Y.*
dc.author.googleKim M.K.*
dc.author.googleMun Y.-C.*
dc.author.googleShin H.-J.*
dc.author.googleKwak J.-Y.*
dc.author.googleKang H.J.*
dc.author.googleWon J.H.*
dc.author.googleKwon J.H.*
dc.author.googlePark E.*
dc.author.googleSuh C.*
dc.author.googleYang D.-H.*
dc.contributor.scopusid문영철(7003363716)*
dc.date.modifydate20240422115947*
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의과대학 > 의학과 > Journal papers
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