Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10609
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dc.contributor.authorMitchell, Paul L Ren
dc.contributor.authorMarlton, Paulaen
dc.contributor.authorGrigg, Andrew Pen
dc.contributor.authorSeymour, John Fen
dc.contributor.authorHertzberg, Marken
dc.contributor.authorEnno, Arnoen
dc.contributor.authorHerrmann, Richarden
dc.contributor.authorBond, Rodneyen
dc.contributor.authorArthur, Chrisen
dc.date.accessioned2015-05-16T00:07:17Z
dc.date.available2015-05-16T00:07:17Z
dc.date.issued2008-05-01en
dc.identifier.citationLeukemia & Lymphoma; 49(5): 924-31en
dc.identifier.govdoc18464112en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10609en
dc.description.abstractLiposomal daunorubicin (DaunoXome) was substituted for doxorubicin in the CHOP regimen, aiming to reduce toxicity and maintain or improve efficacy in elderly patients. Eligibility criteria included: age >or=60 years; previously untreated aggressive non-Hodgkin Lymphoma (NHL) and performance status (PS) 0-2. Treatment was cyclophosphamide 750 mg/m(2), vincristine 1.4 mg/m(2) (maximum 2 mg), and DaunoXome 100 mg/m(2) i.v. on day 1, prednisolone 100 mg po on days 1-5 and G-CSF 5 microg/kg/day sc, for 6-8 cycles. For the 51 patients, median age was 70 years (range 60-88), 94% had diffuse large B-cell lymphoma (DLBCL) and 55% were high-intermediate or high-risk according to the age-adjusted international prognostic index. A mean of 6 cycles was delivered, with dose reductions of DaunoXome in 8.3% of cycles. The combined CR and CRu rate was 65.2%, survival was 566 days and 5-year survival 35%. Three deaths occurred during treatment and may have been related to COP-X. Only 4 (7.8%) of the remaining patients had >or=10% reduction in LVEF. However, 35% of patients were hospitalised during treatment, mostly for febrile neutropenia. The response rate to COP-X was similar to that expected with CHOP, with low cardiac toxicity. The high rate of infectious complications suggests that the DaunoXome dose used may be too high for this patient group. These results support further investigation of this regimen in patients with aggressive NHL.en
dc.language.isoenen
dc.subject.otherAgeden
dc.subject.otherAged, 80 and overen
dc.subject.otherAntineoplastic Combined Chemotherapy Protocols.administration & dosage.toxicityen
dc.subject.otherCyclophosphamide.administration & dosageen
dc.subject.otherDaunorubicin.administration & dosageen
dc.subject.otherHumansen
dc.subject.otherInfection.chemically induceden
dc.subject.otherLiposomesen
dc.subject.otherLymphoma, Large B-Cell, Diffuseen
dc.subject.otherLymphoma, Non-Hodgkin.complications.drug therapy.mortalityen
dc.subject.otherMiddle Ageden
dc.subject.otherPrednisolone.administration & dosageen
dc.subject.otherPrognosisen
dc.subject.otherSurvival Analysisen
dc.subject.otherVincristine.administration & dosageen
dc.titleA phase II study of liposomal daunorubicin, in combination with cyclophosphamide, vincristine and prednisolone, in elderly patients with previously untreated aggressive non-Hodgkin lymphoma.en
dc.typeJournal Articleen
dc.identifier.journaltitleLeukemia & lymphomaen
dc.identifier.affiliationAustin Hospital, Melbourne, Australiaen
dc.identifier.doi10.1080/10428190802007700en
dc.description.pages924-31en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/18464112en
dc.type.austinJournal Articleen
local.name.researcherGrigg, Andrew P
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptClinical Haematology-
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