Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19852
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dc.contributor.authorRoberts, Stuart K-
dc.contributor.authorGazzola, Alessia-
dc.contributor.authorLubel, John-
dc.contributor.authorGow, Paul J-
dc.contributor.authorBell, Sally-
dc.contributor.authorNicoll, Amanda-
dc.contributor.authorDev, Anouk-
dc.contributor.authorFink, Michael A-
dc.contributor.authorSood, Siddharth-
dc.contributor.authorKnight, Virginia-
dc.contributor.authorHong, Thai-
dc.contributor.authorPaul, Eldho-
dc.contributor.authorMishra, Gauri-
dc.contributor.authorMajeed, Ammar-
dc.contributor.authorKemp, William-
dc.date2018-11-05-
dc.date.accessioned2018-11-26T00:51:11Z-
dc.date.available2018-11-26T00:51:11Z-
dc.date.issued2018-11-
dc.identifier.citationScandinavian Journal of Gastroenterology 2018; 53(10-11): 1368-1375en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19852-
dc.description.abstractThe objectives of our study were firstly to characterize the treatment stage migration phenomenon in early (Barcelona Clinic Liver Cancer [BCLC]-0/A) stage hepatocellular carcinoma (HCC) by comparing the efficacy of curative therapies with trans-arterial chemoembolization [TACE] and secondly, determining baseline and on-treatment predictors of survival. All patients within BCLC-0/A stage from six tertiary hospitals who received curative therapy with either resection, transplantation, or ablation or TACE as first-line treatment were included in the analyses. The primary endpoint was overall survival; secondary end-points were transplant-free survival and recurrence-free survival. Between January 2000 and December 2013, we identified 253 BCLC-0/A HCC patients of whom 148 (58.5%) received curative therapy and 105 (41.5%) migrated to TACE. Patients undergoing TACE had lower median survival (2.7 vs. 6.7 years; p < .0001), transplant-free survival (2.6 vs. 4.8 years; p < .0001) and recurrence-free survival (1.3 vs. 2.7 years; p < .001). On multivariate analysis treatment allocation to TACE was an independent prognostic predictor for both lower overall survival (HR 1.70, p = .04) and for HCC recurrence (HR 2.25, p < .001). The main prognostic determinant for each target outcome was Child-Pugh score. Our study confirms that curative treatments should always be preferred when applicable in early-stage HCC, but that in cases where this is not possible, TACE is a reasonable albeit inferior treatment option. In addition, it provides unique prognostic information on a significant proportion of patients with early-stage disease in whom curative therapy is not applicable.en_US
dc.language.isoeng-
dc.subjectBCLC 0/Aen_US
dc.subjectsurvivalen_US
dc.subjecttreatment stage migrationen_US
dc.titleTreatment choice for early-stage hepatocellular carcinoma in real-world practice: impact of treatment stage migration to transarterial chemoembolization and treatment response on survival.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleScandinavian Journal of Gastroenterologyen_US
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Clinical Haematology Department, Alfred Hospital, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Gastroenterology, Eastern Health and Eastern Health Clinical School, Monash University, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Gastroenterology, Royal Melbourne Hospital, Parkville, Australiaen_US
dc.identifier.affiliationDepartment of Gastroenterology, Monash Medical Centre, Clayton, Australiaen_US
dc.identifier.affiliationSurgery (University of Melbourne)en_US
dc.identifier.affiliationDepartment of Gastroenterology, Alfred Hospital, and Monash University, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Gastroenterology, St Vincent's Hospital, Fitzroy, Australiaen_US
dc.identifier.affiliationGastroenterology and Hepatologyen_US
dc.identifier.doi10.1080/00365521.2018.1517277en_US
dc.type.contentTexten_US
dc.identifier.pubmedid30394145-
dc.type.austinJournal Article-
local.name.researcherFink, Michael A
item.languageiso639-1en-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptVictorian Liver Transplant Unit-
crisitem.author.deptSurgery-
crisitem.author.deptVictorian Liver Transplant Unit-
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