Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32871
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dc.contributor.authorSiva, Shankar-
dc.contributor.authorSakyanun, Pitchaya-
dc.contributor.authorMai, Tao-
dc.contributor.authorWong, Wenchang-
dc.contributor.authorLim, Adeline-
dc.contributor.authorLudbrook, Joanna-
dc.contributor.authorBettington, Catherine-
dc.contributor.authorRezo, Angela-
dc.contributor.authorPryor, David-
dc.contributor.authorHardcastle, Nicholas-
dc.contributor.authorKron, Tomas-
dc.contributor.authorHiggs, Braden-
dc.contributor.authorLe, Hien-
dc.contributor.authorSkala, Marketa-
dc.contributor.authorGill, Suki-
dc.contributor.authorEade, Thomas-
dc.contributor.authorAwad, Raef-
dc.contributor.authorSasso, Giuseppe-
dc.contributor.authorVinod, Shalini-
dc.contributor.authorMontgomery, Rebecca-
dc.contributor.authorBall, David-
dc.contributor.authorBressel, Mathias-
dc.date2023-
dc.date.accessioned2023-06-07T01:56:43Z-
dc.date.available2023-06-07T01:56:43Z-
dc.date.issued2023-07-01-
dc.identifier.citationJournal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology 2023 ; 41(19)en_US
dc.identifier.issn1527-7755-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32871-
dc.description.abstractClinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.In a randomized phase II clinical trial, the Trans Tasman Radiation Oncology Group compared single- versus multifraction stereotactic ablative body radiotherapy (SABR) in 90 patients with 133 oligometastases to the lung. The study found no differences in safety, efficacy, systemic immunogenicity, or survival between arms, with single-fraction SABR picked as the winner on the basis of cost-effectiveness. In this article, we report the final updated survival outcome analysis. The protocol mandated no concurrent or post-therapy systemic therapy until progression. Modified disease-free survival (mDFS) was defined as any progression not addressable by local therapy, or death. At a median follow-up of 5.4 years, the 3- and 5-year estimates for overall survival (OS) were 70% (95% CI, 59 to 78) and 51% (95% CI, 39 to 61). There were no significant differences between the multi- and single-fraction arms for OS (hazard ratio [HR], 1.1 [95% CI, 0.6 to 2.0]; P = .81). The 3- and 5-year estimates for disease-free survival were 24% (95% CI, 16 to 33) and 20% (95% CI, 13 to 29), with no differences between arms (HR, 1.0 [95% CI, 0.6 to 1.6]; P = .92). The 3- and 5-year estimates for mDFS were 39% (95% CI, 29 to 49) and 34% (95% CI, 24 to 44), with no differences between arms (HR, 1.0 [95% CI, 0.6 to 1.8]; P = .90). In this patient population, where patients receive SABR in lieu of systemic therapy, one-in-three patients are alive without disease in the long term. There were no differences in outcomes by fractionation schedule.en_US
dc.language.isoeng-
dc.titleLong-Term Outcomes of TROG 13.01 SAFRON II Randomized Trial of Single- Versus Multifraction Stereotactic Ablative Body Radiotherapy for Pulmonary Oligometastases.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Clinical Oncology : Official Journal of the American Society of Clinical Oncologyen_US
dc.identifier.affiliationDepartment of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australiaen_US
dc.identifier.affiliationDepartment of Radiation Oncology, Phramongkutklao Hospital, Bangkok, Thailand.en_US
dc.identifier.affiliationPrincess Alexandra Hospital, Radiation Oncology Centre, Brisbane, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Prince of Wales Hospital, Sydney, Australia.en_US
dc.identifier.affiliationRadiation Oncologyen_US
dc.identifier.affiliationDepartment of Radiation Oncology, Calvary Mater Newcastle, Newcastle, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Royal Brisbane and Women's Hospital, Brisbane, Australia.en_US
dc.identifier.affiliationRadiation Oncology Department, Canberra Hospital, Canberra, Australia.en_US
dc.identifier.affiliationPrincess Alexandra Hospital, Radiation Oncology Centre, Brisbane, Australia.en_US
dc.identifier.affiliationSir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Royal Adelaide Hospital, Adelaide, Australia.en_US
dc.identifier.affiliationRadiation Oncology, Royal Hobart Hospital, Hobart, Australia.en_US
dc.identifier.affiliationDepartment of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, Australia.en_US
dc.identifier.affiliationNorthern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationRadiation Oncology Department, Auckland City Hospital, Auckland, New Zealand.en_US
dc.identifier.affiliationLiverpool Hospital, Cancer Therapy Centre, Sydney, Australia.en_US
dc.identifier.affiliationTROG Cancer Research, Research Development, Newcastle, Australia.en_US
dc.identifier.affiliationCentre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.en_US
dc.identifier.affiliation.;Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia.en_US
dc.identifier.affiliation.;Department of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Australia.en_US
dc.identifier.doi10.1200/JCO.23.00150en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-2840-0658en_US
dc.identifier.orcid0000-0002-1527-5889en_US
dc.identifier.orcid0000-0001-9755-7232en_US
dc.identifier.pubmedid37179526-
dc.description.startpageJCO2300150-
local.name.researcherLim, Adeline
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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