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FET-PET/MRI Based Treatment Planning for Glioblastoma Multiforme in Post-Surgical Patients (FET-TREAT)

FET-PET/MRI Based Treatment Planning for Glioblastoma Multiforme in Post-Surgical Patients (FET-TREAT)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06451042
Acronym
FET-TREAT
Enrollment
11
Registered
2024-06-10
Start date
2024-07-01
Completion date
2025-12-08
Last updated
2025-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastoma Multiforme

Keywords

FET-PET, Glioblastoma, GBM, 0-(2-18F-Fluoroethyl)-L-Tyrosine (FET), Glioma

Brief summary

Glioblastoma multiforme (GBM) represent the most common primary brain malignancy and prognosis remains poor. The most common subtype is glioblastoma which has a 5-year survival rate of approximately 5%. Despite advances in MRI techniques, accurately determining total extent of tumor remains a challenge. The result is incomplete treatment resulting in reduced survival or overtreatment resulting in avoidable treatment related morbidity. A more accurate means of assessing tumor extent is needed to guide management to improve patient survival and quality of life.

Interventions

DIAGNOSTIC_TESTFET-PET/MRI

Radiation planning target volume (PTV) when planned with FET-PET/MRI to PTV when planned with conventional (Standard of Care) MRI only. 0-(2-18F-Fluoroethyl)-L-Tyrosine (FET) 180-200 megabecquerel (MBq) administered intravenously prior to PET/MRI imaging.

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Each participant must meet all of the following inclusion criteria to participate in this study: * ≥ 18 years of age * Diagnosis of glioblastoma multiforme * Post-maximally safe surgical resection * No prior radiation or systemic treatment for high grade glioma * Able to tolerate PET/MRI scan with intravenous contrast * Willing to provide informed consent

Exclusion criteria

All participants meeting any of the following

Design outcomes

Primary

MeasureTime frameDescription
Difference in radiation treatment volume as determined by FET-PET/MRI compared to standard of care MRI.12 monthsVolume difference measured in cubic centimetres

Other

MeasureTime frameDescription
Difference in pre- and post-treatment metabolic tumor volume as determined by FET-PET.12 monthsVolume difference measured in cubic centimetres
Overall and recurrence-free survival post radiation treatment.12 monthsMeasured in months
Quality of life changes pre and post radiation treatment.12 monthsUnits on a scale - Linear Analog Self-Assessment, score minimum = 0, score maximum = 10, higher is better

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026