About this trial
This trial is a single arm study for patients receiving bevacizumab for IDH-wildtype glioblastoma. Patients receiving bevacizumab (an anti-VEGF therapy) will receive PSMA scans to investigate the role of PSMA expression in glioblastoma and its relationship to VEGF expression.
Eligibility criteria
Qualifiers
> 18 year of age
ECOG 0-2
Able to provide informed consent for the study
Minimum of 1 month from completion of radiotherapy with clinical or radiography evidence suggesting residual tumour
Disqualifiers
No major organ impairment that would likely lead to unacceptable toxicities- eg significant cardiac, hepatic, renal or haematologic dysfunction (based on clinician assessment)
Any contraindication to bevacizumab, MRI gadolinium contrast or 68Ga-PSMA-617 radioisotope
Any implant, foreign body, 3T MRI incompatible device or other contraindication to MRI imaging
Does not fulfill PBS requirements for bevacizumab
Trial design
Treatments tested in this trial
- PSMA PET/CT scan
Treatment groups
Locations
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