La Trobe

[18f]-fluoroethyl-L-tyrosine (FET) in glioblastoma (FIG) TROG 18.06 study: Protocol for a prospective, multicentre PET/CT trial

Download (1.65 MB)
journal contribution
posted on 2023-11-10, 01:10 authored by ES Koh, Hui GanHui Gan, Clare SenkoClare Senko, RJ Francis, M Ebert, Sze LeeSze Lee, E Lau, M Khasraw, AK Nowak, DL Bailey, BA Moffat, G Fitt, RJ Hicks, R Coffey, R Verhaak, KM Walsh, EH Barnes, R De Abreu Lourenco, M Rosenthal, L Adda, F Foroudi, A Lasocki, A Moore, PA Thomas, P Roach, M Back, R Leonard, Andrew ScottAndrew Scott

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-[ 18 F]-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

Funding

This work is supported by the Medical Research Future Fund (MRFF) Lifting Clinical Trials and Registries Capacity scheme ((MRF1152501), from the Australian Brain Cancer Mission Innovative Clinical Trials Scheme (MRF9500003) and a Cure Brain Cancer Foundation Innovation Grant (award/grant number N/A). RC acknowledges the support of funding from the National Cancer Institute (R35CA197579 and UH3CA241685). Support is also received from commercial partners Cyclotek for the provision of FET and also Telix Pharmaceuticals.

History

Publication Date

2023-08-04

Journal

BMJ Open

Volume

13

Issue

8

Article Number

bmjopen-2022-071327

Pagination

11p.

Publisher

BMJ Publishing Group

ISSN

2044-6055

Rights Statement

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially,and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.