Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9190
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dc.contributor.authorClarke, Ken
dc.contributor.authorBasser, R Len
dc.contributor.authorUnderhill, Cen
dc.contributor.authorMitchell, Paul L Ren
dc.contributor.authorBartlett, Johnen
dc.contributor.authorCher, Lawrence Men
dc.contributor.authorFindlay, Men
dc.contributor.authorDalley, Den
dc.contributor.authorPell, Men
dc.contributor.authorByrne, Men
dc.contributor.authorGeldard, Hen
dc.contributor.authorHill, J Sen
dc.contributor.authorMaher, Den
dc.contributor.authorFox, R Men
dc.contributor.authorGreen, M Den
dc.contributor.authorKaye, A Hen
dc.date.accessioned2015-05-15T22:11:15Z
dc.date.available2015-05-15T22:11:15Z
dc.date.issued1999-08-01en
dc.identifier.citationJournal of Clinical Oncology; 17(8): 2579-84en
dc.identifier.govdoc10561325en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9190en
dc.description.abstractTo assess the efficacy and toxicity of KRN8602 when administered as an intravenous bolus to patients with recurrent high-grade malignant glioma.Patients with recurrent or persistent anaplastic astrocytoma or glioblastoma multiforme who had not received recent chemotherapy or radiotherapy and were of good performance status (Eastern Cooperative Oncology Group score < or = 2) were treated with an intravenous bolus of 40 mg/m(2) KRN8602 every 28 days. Tumor responses were assessed radiologically and clinically after every second cycle of therapy. Treatment was continued until documented progression or a total of six cycles.A median of three cycles (range, one to six cycles) of KRN8602 was administered to 55 patients, 49 of whom received at least two cycles and were, therefore, assessable for response. The overall response rate (disease stabilization or better) was 43% (95% confidence interval, 29% to 58%). There were three complete responses, one partial response, seven minor responses, and 10 patients with stable disease. The median time to progression was 2 months (range, 1.5 to 37 months) and overall survival was 11 months (range, 1.5 to 40 months). Neutropenia was the most common toxicity, although it was generally of brief duration, and there were only seven episodes of febrile neutropenia in 176 cycles delivered. Nonhematologic toxicity was mostly gastrointestinal (nausea and vomiting, diarrhea) and events were grade 2 or lower except for a single episode of grade 3 vomiting.KRN8602 is an active new agent with minimal toxicity in the treatment of relapsed or refractory high-grade glioma. Further studies with KRN8602 in combination with other cytotoxics and in adjuvant treatment of gliomas are warranted.en
dc.language.isoenen
dc.subject.otherAdolescenten
dc.subject.otherAdulten
dc.subject.otherAgeden
dc.subject.otherAntibiotics, Antineoplastic.adverse effects.therapeutic useen
dc.subject.otherAstrocytoma.drug therapy.mortalityen
dc.subject.otherBrain Neoplasms.drug therapy.mortality.pathologyen
dc.subject.otherCarubicin.adverse effects.analogs & derivatives.therapeutic useen
dc.subject.otherCombined Modality Therapyen
dc.subject.otherFemaleen
dc.subject.otherGlioblastoma.drug therapy.mortalityen
dc.subject.otherHumansen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherNeoplasm Recurrence, Local.drug therapyen
dc.subject.otherNeutropenia.chemically induceden
dc.subject.otherSurvival Analysisen
dc.titleKRN8602 (MX2-hydrochloride): an active new agent for the treatment of recurrent high-grade glioma.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Clinical Oncologyen
dc.identifier.affiliationCentre for Developmental Cancer Therapeutics, Parkville, Victoria (affiliates: Ludwig Institute Oncology Unit, Austin & Repatriation Medical Centre, Australiaen
dc.description.pages2579-84en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/10561325en
dc.type.austinJournal Articleen
local.name.researcherCher, Lawrence M
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptMedical Oncology-
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