Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9375
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dc.contributor.authorHarris, M-
dc.contributor.authorGibbs, P-
dc.contributor.authorCebon, Jonathan S-
dc.contributor.authorJones, R-
dc.contributor.authorSewell, Richard B-
dc.contributor.authorSchelleman, Tony-
dc.contributor.authorAngus, Peter W-
dc.date.accessioned2015-05-15T22:26:54Z
dc.date.available2015-05-15T22:26:54Z
dc.date.issued2001-12-01-
dc.identifier.citationInternal Medicine Journal; 31(9): 517-22en_US
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9375en
dc.description.abstractChemoembolization is often used in the treatment of hepatocellular carcinoma; however, there are limited data on its efficacy in an Australian setting.To review retrospectively the experience of 21 patients with hepatocellular carcinoma who collectively had 36 chemoembolizations performed between October 1995 and February 1999 in a teaching hospital and liver transplant centre in Victoria.Selective catheterization of the right or left hepatic arteries was performed. A mixture of cisplatin 50 mg, epirubicin 50 mg, mitomycin C 10 mg, Lipiodol and gelfoam was injected. Computed tomography (CT) scans were performed at baseline and at 1-3 months after chemoembolization. Outcome measures included response rates, toxicity, progression-free and overall survival.CT response rates: partial response 19% (n = 7), median duration 11 months (range 2+ to 37+); minor response 17% (n = 6), median duration 7 months (1+ to 12+); stable disease 42% (n = 15), median duration 3 months (1+ to 15 months); and progressive disease 22% (n = 8). Major toxicities included one case each of acute renal failure, contrast encephalopathy, gastric ulceration and hepatorenal failure. Median progression-free survival was 3 months (range 0-37+). Median overall survival was 15 months (range 6-50+).Chemoembolization has a role in the palliative treatment of hepatocellular carcinoma. Our response rates and toxicity data are consistent with those in the published literature. However, new treatments are needed and prevention of disease by reduction in the prevalence of chronic hepatitis B and C will be required to significantly reduce mortality from this tumour.en_US
dc.language.isoenen
dc.subject.otherAdulten
dc.subject.otherAgeden
dc.subject.otherCarcinoma, Hepatocellular.therapyen
dc.subject.otherChemoembolization, Therapeutic.adverse effects.methodsen
dc.subject.otherDisease-Free Survivalen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherLiver Neoplasms.therapyen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherRetrospective Studiesen
dc.subject.otherTreatment Outcomeen
dc.titleHepatocellular carcinoma and chemoembolization.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInternal Medicine Journalen_US
dc.identifier.affiliationMedical Oncologyen_US
dc.description.pages517-22en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/11767865en
dc.type.contentTexten_US
dc.type.austinJournal Articleen
local.name.researcherAngus, Peter W
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptSurgery (University of Melbourne)-
crisitem.author.deptHepatopancreatobiliary Surgery-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
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