Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32871
Title: Long-Term Outcomes of TROG 13.01 SAFRON II Randomized Trial of Single- Versus Multifraction Stereotactic Ablative Body Radiotherapy for Pulmonary Oligometastases.
Austin Authors: Siva, Shankar;Sakyanun, Pitchaya;Mai, Tao;Wong, Wenchang;Lim, Adeline ;Ludbrook, Joanna;Bettington, Catherine;Rezo, Angela;Pryor, David;Hardcastle, Nicholas;Kron, Tomas;Higgs, Braden;Le, Hien;Skala, Marketa;Gill, Suki;Eade, Thomas;Awad, Raef;Sasso, Giuseppe;Vinod, Shalini;Montgomery, Rebecca;Ball, David;Bressel, Mathias
Affiliation: Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia
Department of Radiation Oncology, Phramongkutklao Hospital, Bangkok, Thailand.
Princess Alexandra Hospital, Radiation Oncology Centre, Brisbane, Australia.
Department of Radiation Oncology, Prince of Wales Hospital, Sydney, Australia.
Radiation Oncology
Department of Radiation Oncology, Calvary Mater Newcastle, Newcastle, Australia.
Department of Radiation Oncology, Royal Brisbane and Women's Hospital, Brisbane, Australia.
Radiation Oncology Department, Canberra Hospital, Canberra, Australia.
Princess Alexandra Hospital, Radiation Oncology Centre, Brisbane, Australia.
Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia
Department of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Australia.
Department of Radiation Oncology, Royal Adelaide Hospital, Adelaide, Australia.
Radiation Oncology, Royal Hobart Hospital, Hobart, Australia.
Department of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, Australia.
Northern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Radiation Oncology Department, Auckland City Hospital, Auckland, New Zealand.
Liverpool Hospital, Cancer Therapy Centre, Sydney, Australia.
TROG Cancer Research, Research Development, Newcastle, Australia.
Centre for Biostatistics and Clinical Trials, Peter MacCallum Cancer Centre, Melbourne, Australia.
.;Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia.
.;Department of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Australia.
Issue Date: 1-Jul-2023
Date: 2023
Publication information: Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology 2023 ; 41(19)
Abstract: Clinical 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.
URI: https://ahro.austin.org.au/austinjspui/handle/1/32871
DOI: 10.1200/JCO.23.00150
ORCID: 0000-0003-2840-0658
0000-0002-1527-5889
0000-0001-9755-7232
Journal: Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
Start page: JCO2300150
PubMed URL: 37179526
ISSN: 1527-7755
Type: Journal Article
Appears in Collections:Journal articles

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