Hyperpolarized Carbon-13 Alpha-ketoglutarate Metabolic Imaging in IDH Mutant Glioma

Trial ID: NCT05851378

Interventional - Phase 1 - Completed

This study will investigate the use of hyperpolarized (HP) carbon-13 (13C) alpha-ketoglutarate (aKG) (HP 13C-aKG) to characterize tumor burden in participants with isocitrate dehydrogenase (IDH) mutant glioma.

Conditions

• Adult Gliomas, Mixed

Interventions

• Hyperpolarized Carbon 13 Alpha-ketoglutarate (HP C13-aKG)
• Magnetic Resonance Image (MRI)

Eligibility

Inclusion criteria

• 1\. Participants must be \> 18 years old who have evidence of evaluable disease (with contrast enhancing lesion or non-enhancing lesion \> 1 cubic centimetre (cc))
• Cohort 1: Participants with IDH mutant glioma who may or may not have received prior treatment
• Cohort 2: Participants with recurrent IDH mutant glioma before receiving surgical resection,
• All the subjects must have prior MR scans available for review to assess the location and size of residual/recurrent tumor and do not have contraindication for magnetic resonance (MR) examinations. To be included in the study all subjects must also meet the following criteria:
• 1. Participants must have a life expectancy \> 8 weeks.
• 2. Participants must have a Karnofsky performance status of \> 70.
• 3. Participants must have adequate renal function (creatinine \< 1.5 mg/dL). This test must be performed within 60 days prior to the HP 13C Imaging scan.
• 4. Participants must not have any significant medical illnesses that in the investigator's opinion cannot be adequately controlled with appropriate therapy, would compromise the participant's ability to participate in this study or any disease that will obscure toxicity or dangerously impact response to the imaging agent.
• 5. Participants must not have New York Heart Association (NYHA) Grade II or greater congestive heart failure.
• 6. Participants must not have history of myocardial infarction or unstable angina within 12 months prior to study enrollment.
• 7. This study was designed to include women and minorities but was not designed to measure differences of intervention effects. Males and females will be recruited with no preference to gender. Minorities will actively be recruited to participate. No

Exclusion criteria

• 1\. Participants are excluded from participating in this study if they are not able to comply with study procedures.

Sponsor

Robert Bok, MD, PhD, National Cancer Institute (NCI)

Source: ClinicalTrials.gov

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