Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28682
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dc.contributor.authorHirsch, Ryan D-
dc.contributor.authorMills, Chris-
dc.contributor.authorSawhney, Rohit-
dc.contributor.authorSood, Siddharth-
dc.contributor.authorBird, Virginia-
dc.contributor.authorMishra, Gauri-
dc.contributor.authorDev, Anouk-
dc.contributor.authorKemp, William-
dc.contributor.authorLubel, John-
dc.contributor.authorRoberts, Stuart K-
dc.contributor.authorGow, Paul J-
dc.contributor.authorNicoll, Amanda J-
dc.date.accessioned2022-01-28T05:12:12Z-
dc.date.available2022-01-28T05:12:12Z-
dc.date.issued2021-09-
dc.identifier.citationJournal of Gastrointestinal Cancer 2021; 52(3): 907-914en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28682-
dc.description.abstractHepatocellular carcinoma (HCC) is responsible for 1% of deaths worldwide, and the incidence continues to increase. Despite surveillance programs, 70% of HCC patients are not suitable for curative options at diagnosis, and therefore, non-curative treatments are essential to modern clinical practice. There are many novel treatments, though their roles are not well defined. This study aimed to contrast Selective Internal Radiation Therapy (SIRT) and Drug Eluting Bead Transarterial Chemoembolisation (DEB-TACE) to further define their roles. This was a retrospective multicentre cohort study. Factors included for analysis were type of HCC treatment, number of lesions, lesion size, multiple disease severity scores, cirrhosis and vascular invasion. The primary endpoint was transplant-free survival. Transplant-free survival was similar between the two cohorts (p = 0.654), despite a variation in median lesion size, SIRT: 54.5 mm, DEB-TACE: 34 mm (p ≤ 0.001). A univariate Cox proportional hazard model utilising treatment modality as the covariate showed no significant difference in survival (DEB-TACE HR 1.4 (95%CI 0.85-2.15 p = 0.207). The size of the largest lesion was the best predictor of 3-year survival (p = 0.035). Lesion size was inversely associated with survival (HR 1.01 (95%CI 1-1.02, p = 0.025)) on multivariate analysis. This study is the first to catalogue the experience of using SIRT in HCC in a real-world Australian population. It has demonstrated no difference in survival outcomes between DEB-TACE and SIRT. Further, it has shown SIRT to be a reasonable alternative to DEB-TACE especially in larger lesions and has demonstrated that DEB-TACE has a role in select patients with advanced disease.en
dc.language.isoeng-
dc.subjectDrug eluting bead chemoembolisationen
dc.subjectHepatocellular carcinomaen
dc.subjectIntra-arterial therapyen
dc.subjectLiver canceren
dc.subjectSelective internal radiation therapyen
dc.subjectTransarterial radiation therapyen
dc.titleSIRT Compared with DEB-TACE for Hepatocellular Carcinoma: a Real-world Study (the SITAR Study).en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Gastrointestinal Canceren
dc.identifier.affiliationGastroenterology and Hepatologyen
dc.identifier.affiliationGastroenterology, Eastern Health, 3W Box Hill Hospital, Box Hill, VIC, 3128, Australiaen
dc.identifier.affiliationGastroenterology and Hepatology, Melbourne Health, Parkville, Victoria, Australiaen
dc.identifier.affiliationGastroenterology, Monash Health, Clayton, Victoria, Australiaen
dc.identifier.affiliationGastroenterology, Alfred Health, Melbourne, Victoria, Australiaen
dc.identifier.affiliationEastern Health Clinical School, Monash University, Box Hill, Victoria, Australiaen
dc.identifier.affiliationCentral Clinical School, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/32901445/en
dc.identifier.doi10.1007/s12029-020-00502-zen
dc.type.contentTexten
dc.identifier.orcid0000-0003-1283-470Xen
dc.identifier.orcid0000-0001-6505-7233en
dc.identifier.pubmedid32901445-
local.name.researcherGow, Paul J
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
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