Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33476
Title: [18F]-fluoroethyl-L-tyrosine (FET) in glioblastoma (FIG) TROG 18.06 study: protocol for a prospective, multicentre PET/CT trial.
Austin Authors: Koh, Eng-Siew;Gan, Hui K ;Senko, Clare ;Francis, Roslyn J;Ebert, Martin;Lee, Sze Ting ;Lau, Eddie ;Khasraw, Mustafa;Nowak, Anna K;Bailey, Dale L;Moffat, Bradford A;Fitt, Gregory J ;Hicks, Rodney J;Coffey, Robert;Verhaak, Roel;Walsh, Kyle M;Barnes, Elizabeth H;De Abreu Lourenco, Richard;Rosenthal, Mark;Adda, Lucas;Foroudi, Farshad ;Lasocki, Arian;Moore, Alisha;Thomas, Paul A;Roach, Paul;Back, Michael;Leonard, Robyn;Scott, Andrew M 
Affiliation: Radiation Oncology, Liverpool Hospital, Liverpool, New South Wales, Australia.;South West Sydney Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
Medical Oncology
School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.;Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia.;Department of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australia.
Department of Nuclear Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.;Medical School, The University of Western Australia, Crawley, Western Australia, Australia.
Department of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.;School of Physics, Mathematics and Computing, University of Western Australia, Crawley, Western Australia, Australia.
School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.;Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia.;School of Medicine, University of Melbourne, Melbourne, Victoria, Australia.;Department of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australia.
Molecular Imaging and Therapy
Department of Neurosurgery and Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, North Carolina, USA.
Medical School, The University of Western Australia, Crawley, Western Australia, Australia.;Department of Medical Oncology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
Faculty of Medicine & Health, University of Sydney, Camperdown, New South Wales, Australia.;Department of Nuclear Medicine, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
Melbourne Brain Centre Imaging Unit, Department of Radiology, University of Melbourne, Melbourne, Victoria, Australia.
Radiology
Department of Radiology, University of Melbourne, Melbourne, Victoria, Australia.;Centre for Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.
Epithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Department of Neurosurgery, Yale School of Medicine, New Haven, Connecticut, USA.;Department of Neurosurgery, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Department of Neurosurgery and Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, North Carolina, USA.
NHMRC Clinical Trials Centre, The University of Sydney, Sydney, New South Wales, Australia.
Centre for Health Economics Research and Evaluation, University of Technology Sydney, Broadway, New South Wales, Australia.
School of Medicine, University of Melbourne, Melbourne, Victoria, Australia.;Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
The Cooperative Trials Group for Neuro-Oncology (COGNO) Consumer Advisor Panel, National Health and Medical Research Council (NHMRC) Clinical Trials Centre (CTC), University of Sydney, Sydney, New South Wales, Australia.
School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.;Department of Radiation Oncology, Austin Health, Melbourne, Victoria, Australia.
Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.;Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.
Trans Tasman Radiation Oncology Group (TROG), Newcastle, New South Wales, Australia.
Department of Nuclear Medicine, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.;Faculty of Medicine, The University of Queensland, Saint Lucia, Queensland, Australia.
Department of Nuclear Medicine, Royal North Shore Hospital, St Leonards, New South Wales, Australia.;The University of Sydney, Camperdown, New South Wales, Australia.
Department of Radiation Oncology, Royal North Shore Hospital, St Leonards, New South Wales, Australia.;Faculty of Medicine & Health, University of Sydney, Sydney, New South Wales, Australia.
NHMRC Clinical Trials Centre, The University of Sydney, Sydney, New South Wales, Australia.
School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.;Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia.;School of Medicine, University of Melbourne, Melbourne, Victoria, Australia.;Department of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australia.
Issue Date: 4-Aug-2023
Date: 2023
Publication information: BMJ Open 2023-08-04; 13(8)
Abstract: Glioblastoma is the most common aggressive primary central nervous system cancer in adults characterised by uniformly poor survival. Despite maximal safe resection and postoperative radiotherapy with concurrent and adjuvant temozolomide-based chemotherapy, tumours inevitably recur. Imaging with O-(2-[18F]-fluoroethyl)-L-tyrosine (FET) positron emission tomography (PET) has the potential to impact adjuvant radiotherapy (RT) planning, distinguish between treatment-induced pseudoprogression versus tumour progression as well as prognostication. The FET-PET in Glioblastoma (FIG) study is a prospective, multicentre, non-randomised, phase II study across 10 Australian sites and will enrol up to 210 adults aged ≥18 years with newly diagnosed glioblastoma. FET-PET will be performed at up to three time points: (1) following initial surgery and prior to commencement of chemoradiation (FET-PET1); (2) 4 weeks following concurrent chemoradiation (FET-PET2); and (3) within 14 days of suspected clinical and/or radiological progression on MRI (performed at the time of clinical suspicion of tumour recurrence) (FET-PET3). The co-primary outcomes are: (1) to investigate how FET-PET versus standard MRI impacts RT volume delineation and (2) to determine the accuracy and management impact of FET-PET in distinguishing pseudoprogression from true tumour progression. The secondary outcomes are: (1) to investigate the relationships between FET-PET parameters (including dynamic uptake, tumour to background ratio, metabolic tumour volume) and progression-free survival and overall survival; (2) to assess the change in blood and tissue biomarkers determined by serum assay when comparing FET-PET data acquired prior to chemoradiation with other prognostic markers, looking at the relationships of FET-PET versus MRI-determined site/s of progressive disease post chemotherapy treatment with MRI and FET-PET imaging; and (3) to estimate the health economic impact of incorporating FET-PET into glioblastoma management and in the assessment of post-treatment pseudoprogression or recurrence/true progression. Exploratory outcomes include the correlation of multimodal imaging, blood and tumour biomarker analyses with patterns of failure and survival. The study protocol V.2.0 dated 20 November 2020 has been approved by a lead Human Research Ethics Committee (Austin Health, Victoria). Other clinical sites will provide oversight through local governance processes, including obtaining informed consent from suitable participants. The study will be conducted in accordance with the principles of the Declaration of Helsinki and Good Clinical Practice. Results of the FIG study (TROG 18.06) will be disseminated via relevant scientific and consumer forums and peer-reviewed publications. ANZCTR ACTRN12619001735145.
URI: https://ahro.austin.org.au/austinjspui/handle/1/33476
DOI: 10.1136/bmjopen-2022-071327
ORCID: 0000-0002-1664-2513
0000-0001-7319-8546
0000-0002-5232-4491
0000-0002-6256-1351
0000-0002-6875-0719
0000-0001-8641-456X
0000-0002-1261-7775
0000-0003-3249-9849
0000-0002-9317-9526
0000-0001-9154-7957
0000-0002-0278-4801
0000-0002-1512-9654
0000-0002-0758-0824
0000-0002-2180-3844
0000-0003-2773-0436
0000-0002-5879-9981
0000-0001-7435-5128
0000-0002-5978-8774
0000-0003-1152-6764
0000-0002-8562-364X
0000-0001-8387-0965
0000-0001-8176-3015
0000-0002-3981-9289
0000-0002-2420-0950
0000-0003-2504-0474
0000-0003-2363-8333
0000-0003-4454-7617
0000-0002-6656-295X
Journal: BMJ Open
Start page: e071327
PubMed URL: 37541751
ISSN: 2044-6055
Type: Journal Article
Subjects: FET
Glioblastoma
chemoradiation
prognostic marker
pseudoprogression
Glioblastoma/diagnostic imaging
Glioblastoma/therapy
Glioblastoma/pathology
Brain Neoplasms/diagnostic imaging
Brain Neoplasms/therapy
Brain Neoplasms/pathology
Neoplasm Recurrence, Local/diagnostic imaging
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