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[18F]-fluoroethyl-L-tyrosine (FET) in glioblastoma (FIG) TROG 18.06 study: protocol for a prospective, multicentre PET/CT trial.
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, Greg; 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.
Afiliação
  • Koh ES; Radiation Oncology, Liverpool Hospital, Liverpool, New South Wales, Australia EngSiew.Koh@health.nsw.gov.au.
  • Gan HK; South West Sydney Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
  • Senko C; Austin Health, Department of Medical Oncology, Melbourne, Victoria, Australia.
  • Francis RJ; School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.
  • Ebert M; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia.
  • Lee ST; School of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Lau E; School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.
  • Khasraw M; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia.
  • Nowak AK; Department of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australia.
  • Bailey DL; Department of Nuclear Medicine, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Moffat BA; Medical School, The University of Western Australia, Crawley, Western Australia, Australia.
  • Fitt G; Department of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.
  • Hicks RJ; School of Physics, Mathematics and Computing, University of Western Australia, Crawley, Western Australia, Australia.
  • Coffey R; School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.
  • Verhaak R; Tumour Targeting Program, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia.
  • Walsh KM; School of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Barnes EH; Department of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australia.
  • De Abreu Lourenco R; Department of Molecular Imaging and Therapy, Austin Health, Heidelberg, Victoria, Australia.
  • Rosenthal M; Department of Radiology, University of Melbourne, Melbourne, Victoria, Australia.
  • Adda L; Department of Radiology, Austin Health, Heidelberg, Victoria, Australia.
  • Foroudi F; Department of Neurosurgery and Preston Robert Tisch Brain Tumor Center, Duke University School of Medicine, Durham, North Carolina, USA.
  • Lasocki A; Medical School, The University of Western Australia, Crawley, Western Australia, Australia.
  • Moore A; Department of Medical Oncology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Thomas PA; Faculty of Medicine & Health, University of Sydney, Camperdown, New South Wales, Australia.
  • Roach P; Department of Nuclear Medicine, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
  • Back M; Melbourne Brain Centre Imaging Unit, Department of Radiology, University of Melbourne, Melbourne, Victoria, Australia.
  • Leonard R; Department of Radiology, University of Melbourne, Melbourne, Victoria, Australia.
  • Scott AM; Department of Radiology, Austin Health, Heidelberg, Victoria, Australia.
BMJ Open ; 13(8): e071327, 2023 08 04.
Article em En | MEDLINE | ID: mdl-37541751
INTRODUCTION: 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. METHODS AND ANALYSIS: 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. ETHICS AND DISSEMINATION: 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. TRIAL REGISTRATION NUMBER: ANZCTR ACTRN12619001735145.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma / Ficus Tipo de estudo: Clinical_trials / Guideline / Observational_studies Limite: Adolescent / Adult / Humans País/Região como assunto: Oceania Idioma: En Revista: BMJ Open Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma / Ficus Tipo de estudo: Clinical_trials / Guideline / Observational_studies Limite: Adolescent / Adult / Humans País/Região como assunto: Oceania Idioma: En Revista: BMJ Open Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Austrália