Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33758
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dc.contributor.authorLiu, H Y-H-
dc.contributor.authorLee, Y-Y D-
dc.contributor.authorSridharan, S-
dc.contributor.authorWang, W-
dc.contributor.authorKhor, R-
dc.contributor.authorChu, J-
dc.contributor.authorOar, A-
dc.contributor.authorChoong, E S-
dc.contributor.authorLe, H-
dc.contributor.authorShanker, M-
dc.contributor.authorWigg, A-
dc.contributor.authorStuart, K-
dc.contributor.authorPryor, D-
dc.date2023-
dc.date.accessioned2023-09-20T07:00:09Z-
dc.date.available2023-09-20T07:00:09Z-
dc.date.issued2023-12-
dc.identifier.citationClinical Oncology (Royal College of Radiologists (Great Britain)) 2023-12; 35(12)en_US
dc.identifier.issn1433-2981-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33758-
dc.description.abstractStandard curative options for early-stage, solitary hepatocellular carcinoma (HCC) are often unsuitable due to liver dysfunction, comorbidities and/or tumour location. Stereotactic body radiation therapy (SBRT) has shown high rates of local control in HCC; however, limited data exist in the treatment-naïve, curative-intent setting. We report the outcomes of patients with solitary early-stage HCC treated with SBRT as first-line curative-intent therapy. A multi-institutional retrospective study of treatment-naïve patients with Barcelona Clinic Liver Cancer stage 0/A, solitary ≤5 cm HCC, Child-Pugh score (CPS) A liver function who underwent SBRT between 2010 and 2019 as definitive therapy. The primary end point was freedom from local progression. Secondary end points were progression-free survival, overall survival, rate of treatment-related clinical toxicities and change in CPS >1. In total, 68 patients were evaluated, with a median follow-up of 20 months (range 3-58). The median age was 68 years (range 50-86); 54 (79%) were men, 62 (91%) had cirrhosis and 50 (74%) were Eastern Cooperative Oncology Group 0. The median HCC diameter was 2.5 cm (range 1.3-5) and the median prescription biologically effective dose with a tumour a/b ratio of 10 Gy (BED10) was 93 Gy (interquartile range 72-100 Gy). Two-year freedom from local progression, progression-free survival and overall survival were 94.3% (95% confidence interval 86.6-100%), 59.5% (95% confidence interval 46.3-76.4%) and 88% (95% confidence interval 79.2-97.6%), respectively. Nine patients (13.2%) experienced grade ≥2 treatment-related clinical toxicities. A rise >1 in CPS was observed in six cirrhotic patients (9.6%). SBRT is an effective and well-tolerated option to consider in patients with solitary, early-stage HCC. Prospective, randomised comparative studies are warranted to further refine its role as a first-line curative-intent therapy.en_US
dc.language.isoeng-
dc.subjectCurative intenten_US
dc.subjectHepatocellular carcinomaen_US
dc.subjectStereotactic ablative radiation therapyen_US
dc.subjectStereotactic body radiation therapyen_US
dc.titleDefinitive Stereotactic Body Radiation Therapy in Early-Stage Solitary Hepatocellular Carcinoma: An Australian Multi-Institutional Review of Outcomes.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleClinical Oncology (Royal College of Radiologists (Great Britain))en_US
dc.identifier.affiliationDepartment of Cancer Services, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia; Faculty of Medicine, University of Queensland, St. Lucia, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Cancer Services, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia; Faculty of Medicine, University of Queensland, St. Lucia, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Calvary Mater Newcastle, Waratah, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, The Crown Princess Mary Cancer Centre, Westmead, New South Wales, Australia; Department of Radiation Oncology, Nepean Cancer Care Centre, Kingswood, New South Wales, Australia.en_US
dc.identifier.affiliationOlivia Newton-John Cancer Wellness and Research Centreen_US
dc.identifier.affiliationDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationIcon Cancer Centre, Gold Coast University Hospital, Gold Coast, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Chris O'Brien Lifehouse, Camperdown, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Central Adelaide Local Health Network, Adelaide, South Australia, Australia; South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia; Clinical and Health Sciences, University of South Australia, Adelaide, South Australia, Australia.en_US
dc.identifier.affiliationDepartment of Cancer Services, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia; Faculty of Medicine, University of Queensland, St. Lucia, Queensland, Australia.en_US
dc.identifier.affiliationHepatology and Liver Transplantation Medicine Unit, Flinders Medical Centre, Adelaide, South Australia, Australia.en_US
dc.identifier.affiliationDepartment of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Cancer Services, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia; Faculty of Medicine, University of Queensland, St. Lucia, Queensland, Australia.en_US
dc.identifier.affiliationRadiation Oncologyen_US
dc.identifier.doi10.1016/j.clon.2023.08.012en_US
dc.type.contentTexten_US
dc.identifier.pubmedid37709623-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
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