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PET and MRI Imaging of Brain Tumors Using [18F]PARPi

Early Phase 1
Active, not recruiting
Conditions
Brain Cancer
Brain Tumor
Interventions
Diagnostic Test: PET/MR with [18F]PARPi
Drug: [18F]PARPi
Registration Number
NCT04173104
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

This study is to collect data about how 18FPARPi can be used together with PET/positron emission tomography and MRI/magnetic resonance imaging scans to take pictures of brain cancer

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
5
Inclusion Criteria
  • Patients with new or suspected recurrent brain tumors (including suspected recurrent brain tumors showing growth from any preceding scan)
  • Age >/= 18 years
  • Minimum at least one brain lesion size >/= 1.5cm diameter
  • Scheduled to undergo treatment at MSK
  • Willingness to sign informed consent
  • Able to receive intravenous gadolinium contrast per MSK Department of Radiology guidelines
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Exclusion Criteria
  • Any contraindication to 3T MRI (PET/MR scanner is 4.0 Tesla)
  • Pregnancy or breast-feeding women
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Participants with Brain CancerPET/MR with [18F]PARPiParticipants with new or suspected recurrent brain tumors
Participants with Brain Cancer[18F]PARPiParticipants with new or suspected recurrent brain tumors
Primary Outcome Measures
NameTimeMethod
SUVmax measurementsUp to 24 weeks

\[18F\]PARPi updtake in lesions will be quantified by standard SUVmax measurements from PET/MR scans

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

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