Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/42157
Full metadata record
DC FieldValueLanguage
dc.contributor.authorHumphrey K.en
dc.contributor.authorDohner H.en
dc.contributor.authorAsikanius E.en
dc.contributor.authorWenger M.K.en
dc.contributor.authorGoede V.en
dc.contributor.authorHallek M.en
dc.contributor.authorFischer K.en
dc.contributor.authorBusch R.en
dc.contributor.authorEngelke A.en
dc.contributor.authorEichhorst B.en
dc.contributor.authorWendtner C.M.en
dc.contributor.authorChagorova T.en
dc.contributor.authorDela Serna J.en
dc.contributor.authorDilhuydy M.S.en
dc.contributor.authorOpat S.en
dc.contributor.authorOwen C.J.en
dc.contributor.authorSamoylova O.en
dc.contributor.authorKreuzer K.A.en
dc.contributor.authorLangerak A.W.en
dc.contributor.authorRitgen M.en
dc.contributor.authorStilgenbauer S.en
dc.date.accessioned2021-05-14T14:27:37Zen
dc.date.available2021-05-14T14:27:37Zen
dc.date.copyright2014en
dc.date.created20150304en
dc.date.issued2015-03-12en
dc.identifier.citationBritish Journal of Haematology. Conference: 54th Annual Scientific Meeting of the British Society for Haematology. Birmingham United Kingdom. Conference Publication: (var.pagings). 165 (SUPPL. 1) (pp 19), 2014. Date of Publication: May 2014.en
dc.identifier.issn0007-1048en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/42157en
dc.description.abstractCLL11 is a phase 3 trial investigating first-line chemoimmunotherapy in CLL patients with comorbidities. Here, we present published results of the head-to-head comparison between GA101 plus Clb (G-Clb) and rituximab plus Clb (R-Clb), and of the G-Clb versus Clb and R-Clb versus Clb comparisons. Treatment-naive CLL patients with a CIRS score >6 and/or a CrCl <70 ml/min were eligible. Patients received Clb alone (0.5 mg/kg po d1, d15 q28 days, 6 cycles), G-Clb (100 mg iv d1, 900 mg d2, 1000 mg d8, d15 of cycle 1, 1000 mg d1 cycles 2-6), or R-Clb (375 mg/m2 iv d1 cycle 1, 500 mg/m2 d1 cycles 2-6). The G-Clb and R-Clb treatment arms were well balanced for baseline characteristics. Median age, CIRS score, and CrCl at baseline were 73 years, 8, and 62 ml/min respectively. Key results of the G-Clb versus R-Clb comparison are shown in the table. The number of patients with MRD negative blood samples at end-of-treatment was significantly higher with G-Clb compared with R-Clb. OS analysis demonstrated a benefit of G-Clb over Clb alone. In conclusion, GA101, a novel, glycoengineered, type II CD20 antibody, in combination with Clb improved outcomes compared with R-Clb in previously untreated CLL patients with comorbidities. (Table presented) .en
dc.languageenen
dc.languageEnglishen
dc.publisherBlackwell Publishing Ltden
dc.titleObinutuzumab (GA101) plus chlorambucil (Clb) versus rituximab plus Clb in patients with chronic lymphocytic leukaemia (CLL) and comorbidities: Recently published results of the CLL11 trial.en
dc.typeConference Abstracten
dc.identifier.affiliationHaematologyen
dc.type.studyortrialClinical trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/bjh.12802en
local.date.conferencestart2014-04-28en
dc.identifier.source71802705en
dc.identifier.institution(Goede, Fischer, Wendtner) Department of Internal Medicine, Center of Integrated Oncology Cologne-Bonn, University Hospital Cologne, Cologne, Germany (Busch) Institute of Medical Statistics and Epidemiology, Technical University Munich, Munich, Germany (Engelke, Eichhorst, Kreuzer, Hallek) Department I of Internal Medicine, Center of Integrated Oncology Cologne-Bonn, University Hospital Cologne, Cologne, Germany (Wendtner) Klinikum Schwabing, Munich, Germany (Chagorova) Penza Regional Oncology Dispensary, Russian Federation (Dela Serna) Servicio De Hematologia, Hospital Univ 12 De Octubre, Madrid, Spain (Dilhuydy) Hopital Haut Leveque, Bordeaux, Pessac, France (Opat) Department of Haematology, Monash Medical Centre, Clayton, ON, Australia (Owen) University of Calgary, Calgary, AB, Canada (Samoylova) Regional Clinical Hospital N.A. Semashko, Nizhny Novgorod, Russian Federation (Langerak) Department of Immunology, Erasmus Medical Center Rotterdam, Rotterdam, Netherlands (Ritgen) Medical Department II, University of Schleswig Holstein, City Hospital Kiel, Kiel, Germany (Stilgenbauer, Dohner) Department of Internal Medicine III, University Hospital of Ulm, Ulm, Germany (Asikanius) F. Hoffmann-La Roche Ltd, Basel, Switzerland (Humphrey) F. Hoffmann-La Roche Ltd, Welwyn, United Kingdom (Wenger) Genentech, Inc., South San Francisco, CA, United Statesen
dc.description.addressV. Goede, Department of Internal Medicine, Center of Integrated Oncology Cologne-Bonn, University Hospital Cologne, Cologne, Germanyen
dc.description.publicationstatusCONFERENCE ABSTRACTen
local.date.conferenceend2014-04-30en
dc.rights.statementCopyright 2015 Elsevier B.V., All rights reserved.en
dc.identifier.affiliationext(Goede, Fischer, Wendtner) Department of Internal Medicine, Center of Integrated Oncology Cologne-Bonn, University Hospital Cologne, Cologne, Germany-
dc.identifier.affiliationext(Busch) Institute of Medical Statistics and Epidemiology, Technical University Munich, Munich, Germany-
dc.identifier.affiliationext(Engelke, Eichhorst, Kreuzer, Hallek) Department I of Internal Medicine, Center of Integrated Oncology Cologne-Bonn, University Hospital Cologne, Cologne, Germany-
dc.identifier.affiliationext(Wendtner) Klinikum Schwabing, Munich, Germany-
dc.identifier.affiliationext(Chagorova) Penza Regional Oncology Dispensary, Russian Federation-
dc.identifier.affiliationext(Dela Serna) Servicio De Hematologia, Hospital Univ 12 De Octubre, Madrid, Spain-
dc.identifier.affiliationext(Dilhuydy) Hopital Haut Leveque, Bordeaux, Pessac, France-
dc.identifier.affiliationext(Owen) University of Calgary, Calgary, AB, Canada-
dc.identifier.affiliationext(Samoylova) Regional Clinical Hospital N.A. Semashko, Nizhny Novgorod, Russian Federation-
dc.identifier.affiliationext(Langerak) Department of Immunology, Erasmus Medical Center Rotterdam, Rotterdam, Netherlands-
dc.identifier.affiliationext(Ritgen) Medical Department II, University of Schleswig Holstein, City Hospital Kiel, Kiel, Germany-
dc.identifier.affiliationext(Stilgenbauer, Dohner) Department of Internal Medicine III, University Hospital of Ulm, Ulm, Germany-
dc.identifier.affiliationext(Asikanius) F. Hoffmann-La Roche Ltd, Basel, Switzerland-
dc.identifier.affiliationext(Humphrey) F. Hoffmann-La Roche Ltd, Welwyn, United Kingdom-
dc.identifier.affiliationext(Wenger) Genentech, Inc., South San Francisco, CA, United States-
dc.identifier.affiliationmh(Opat) Department of Haematology, Monash Medical Centre, Clayton, ON, Australia-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeConference Abstract-
crisitem.author.deptHaematology-
Appears in Collections:Conferences
Show simple item record

Page view(s)

12
checked on Feb 6, 2025

Google ScholarTM

Check


Items in Monash Health Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.