Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33476
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dc.contributor.authorKoh, Eng-Siew-
dc.contributor.authorGan, Hui K-
dc.contributor.authorSenko, Clare-
dc.contributor.authorFrancis, Roslyn J-
dc.contributor.authorEbert, Martin-
dc.contributor.authorLee, Sze Ting-
dc.contributor.authorLau, Eddie-
dc.contributor.authorKhasraw, Mustafa-
dc.contributor.authorNowak, Anna K-
dc.contributor.authorBailey, Dale L-
dc.contributor.authorMoffat, Bradford A-
dc.contributor.authorFitt, Gregory J-
dc.contributor.authorHicks, Rodney J-
dc.contributor.authorCoffey, Robert-
dc.contributor.authorVerhaak, Roel-
dc.contributor.authorWalsh, Kyle M-
dc.contributor.authorBarnes, Elizabeth H-
dc.contributor.authorDe Abreu Lourenco, Richard-
dc.contributor.authorRosenthal, Mark-
dc.contributor.authorAdda, Lucas-
dc.contributor.authorForoudi, Farshad-
dc.contributor.authorLasocki, Arian-
dc.contributor.authorMoore, Alisha-
dc.contributor.authorThomas, Paul A-
dc.contributor.authorRoach, Paul-
dc.contributor.authorBack, Michael-
dc.contributor.authorLeonard, Robyn-
dc.contributor.authorScott, Andrew M-
dc.date2023-
dc.date.accessioned2023-08-09T04:43:10Z-
dc.date.available2023-08-09T04:43:10Z-
dc.date.issued2023-08-04-
dc.identifier.citationBMJ Open 2023-08-04; 13(8)en_US
dc.identifier.issn2044-6055-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33476-
dc.description.abstractGlioblastoma 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.en_US
dc.language.isoeng-
dc.subjectFETen_US
dc.subjectGlioblastomaen_US
dc.subjectchemoradiationen_US
dc.subjectprognostic markeren_US
dc.subjectpseudoprogressionen_US
dc.title[18F]-fluoroethyl-L-tyrosine (FET) in glioblastoma (FIG) TROG 18.06 study: protocol for a prospective, multicentre PET/CT trial.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBMJ Openen_US
dc.identifier.affiliationRadiation Oncology, Liverpool Hospital, Liverpool, New South Wales, Australia.;South West Sydney Clinical School, University of New South Wales, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationMedical Oncologyen_US
dc.identifier.affiliationSchool 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.en_US
dc.identifier.affiliationDepartment of Nuclear Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.;Medical School, The University of Western Australia, Crawley, Western Australia, Australia.en_US
dc.identifier.affiliationDepartment 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.en_US
dc.identifier.affiliationSchool 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.en_US
dc.identifier.affiliationMolecular Imaging and Therapyen_US
dc.identifier.affiliationDepartment of Neurosurgery and Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, North Carolina, USA.en_US
dc.identifier.affiliationMedical School, The University of Western Australia, Crawley, Western Australia, Australia.;Department of Medical Oncology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.en_US
dc.identifier.affiliationFaculty 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.en_US
dc.identifier.affiliationMelbourne Brain Centre Imaging Unit, Department of Radiology, University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationRadiologyen_US
dc.identifier.affiliationDepartment of Radiology, University of Melbourne, Melbourne, Victoria, Australia.;Centre for Cancer Imaging, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationEpithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, USA.en_US
dc.identifier.affiliationDepartment of Neurosurgery, Yale School of Medicine, New Haven, Connecticut, USA.;Department of Neurosurgery, Amsterdam University Medical Center, Amsterdam, The Netherlands.en_US
dc.identifier.affiliationDepartment of Neurosurgery and Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, North Carolina, USA.en_US
dc.identifier.affiliationNHMRC Clinical Trials Centre, The University of Sydney, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationCentre for Health Economics Research and Evaluation, University of Technology Sydney, Broadway, New South Wales, Australia.en_US
dc.identifier.affiliationSchool of Medicine, University of Melbourne, Melbourne, Victoria, Australia.;Department of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationThe 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.en_US
dc.identifier.affiliationSchool of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.;Department of Radiation Oncology, Austin Health, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationDepartment of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.;Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationTrans Tasman Radiation Oncology Group (TROG), Newcastle, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment of Nuclear Medicine, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.;Faculty of Medicine, The University of Queensland, Saint Lucia, Queensland, Australia.en_US
dc.identifier.affiliationDepartment of Nuclear Medicine, Royal North Shore Hospital, St Leonards, New South Wales, Australia.;The University of Sydney, Camperdown, New South Wales, Australia.en_US
dc.identifier.affiliationDepartment 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.en_US
dc.identifier.affiliationNHMRC Clinical Trials Centre, The University of Sydney, Sydney, New South Wales, Australia.en_US
dc.identifier.affiliationSchool 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.en_US
dc.identifier.doi10.1136/bmjopen-2022-071327en_US
dc.type.contentTexten_US
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dc.identifier.pubmedid37541751-
dc.description.volume13-
dc.description.issue8-
dc.description.startpagee071327-
dc.subject.meshtermssecondaryGlioblastoma/diagnostic imaging-
dc.subject.meshtermssecondaryGlioblastoma/therapy-
dc.subject.meshtermssecondaryGlioblastoma/pathology-
dc.subject.meshtermssecondaryBrain Neoplasms/diagnostic imaging-
dc.subject.meshtermssecondaryBrain Neoplasms/therapy-
dc.subject.meshtermssecondaryBrain Neoplasms/pathology-
dc.subject.meshtermssecondaryNeoplasm Recurrence, Local/diagnostic imaging-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptMedical Oncology-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptRadiology-
crisitem.author.deptRadiology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
crisitem.author.deptRadiation Oncology-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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