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Evaluation of Brain Metastases Treated With Stereotactic Radiotherapy Using Dynamic [18F]FDG PET

Not Applicable
Not yet recruiting
Conditions
Brain Metastases
Interventions
Diagnostic Test: dynamic [18-FDG PET] scan post stereotactic radiation for brain metastases
Registration Number
NCT06511323
Lead Sponsor
Lawson Health Research Institute
Brief Summary

The purpose of this study is to evaluate the clinical usefulness of dynamic \[18F\]FDG PET imaging in assessing brain metastasis post stereotactic radiotherapy to separate true progression from the treatment-related changes.

Detailed Description

After being informed about the study and potential risk, all participants giving written informed consent will be screened to determine if participant being referred fits eligibility criteria for the study, under of the supervision of the radiation oncologist. If a participant agrees to participate in this study, they will receive three additional imaging sessions (the dynamic PET scan). The first session will occur prior to starting treatment; the second session will occur at about 10 weeks post treatment; the third session will occur at first concern of progression at treated lesions or 12 months post-treatment, whichever comes earlier. These scans will be scheduled in addition to the participant's regular follow-up scans and appointments.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
70
Inclusion Criteria
  • Age 18 or older.
  • Willing and able to provide consent.
  • ECOG 0-2.
  • Life expectancy ≥12 months.
  • Creatinine clearance ≥30 ml/min within 28 days prior to registration.
  • At the discretion of the treating oncologist, it is believed that at least 1 lesion (or resection cavity) is best managed with SRS/SFR
Exclusion Criteria
  • Pregnant or nursing women.
  • Men or women of childbearing potential who are unwilling to employ adequate contraception.
  • Inability to complete a brain MRI.
  • Known allergy to gadolinium.
  • Inability to complete a PET scan.
  • Uncontrolled diabetes mellitus.
  • Primary germ cell tumour, primary CNS tumour, or lymphoma
  • SRS/FSRT is no longer indicated for any BMs
  • Must be able to read and write English

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Observationaldynamic [18-FDG PET] scan post stereotactic radiation for brain metastasesThis is a prospective, single-arm, pilot diagnostic study to evaluate the diagnostic accuracy of using dynamic \[18F\]FDG PET in 70 patients with brain metastases managed with stereotactic radiosurgery(SRS)/fractionated stereotactic radiotherapy (FSRT). The study will include imaging assessments at baseline, at 10 weeks after treatment, and at first concern for progression or 12 months post-treatment, whichever comes earlier.
Primary Outcome Measures
NameTimeMethod
Diagnostic accuracy of dynamic PET12-month follow-up.

Diagnostic accuracy will be calculated and compared based on the index lesion.

Secondary Outcome Measures
NameTimeMethod
Cost-effectiveness analysis24-month follow-up

A decision analysis model coupled with Markov model will be constructed to estimate the incremental cost-effectiveness ratio (ICER) of performing dynamic PET in this setting from the Canadian health-care system perspective.

Clinical outcomes24-month follow-up

Factors impact on these outcomes will be explored.

Diagnostic imaging outcomes24-month follow-up

Other ancillary clinical data will be explored.

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