FDG and FDOPA PET Demonstration of Functional Brain Abnormalities

Glioblastoma Clinical Trial

Official title:

FDG and FDOPA PET Demonstration of Functional Brain Abnormalities

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04315584
• Other study ID #: HSR190096
• Status: Recruiting
• Phase: Early Phase 1
• Start date: March 15, 2020
• Est. completion date: June 20, 2024

Study information

• Verified date: March 2020
• Source: University of Virginia
• Contact: Bijoy Kundu, PhD
• Phone: (434) 924-0284
• Email: bkk5a[@]virginia.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this pilot study will be to conduct a clinical trial using a time-of-flight PET scanner and MRI scanner to test an improved method for differentiating tumor recurrence from radiation necrosis in glioblastoma patients. We will attempt to do so by performing a static and dynamic FDG-PET scan, a static and dynamic FDOPA-PET scan, and a multiparametric MRI scan - then comparing the results with surgical pathology and static FDG-PET scans. We hypothesize that the new quantitative kinetic analytical methods using FDOPA in combination with FDG will provide crucial functional information to distinguish recurrent tumors from treatment-induced radiation changes in patients with treated brain neoplasms. This is important for improving patient outcomes by allowing treating physicians to more accurately tailor treatments. Furthermore, dynamic FDG and FDOPA PET will be combined with high resolution anatomic and physiologic MRI in order to develop a multimodal multiparametric approach for differentiating tumor recurrence from treatment effect.

Description:

PRIMARY OBJECTIVES:

I. The primary objective will be to evaluate the diagnostic accuracy of Dynamic PET imaging in differentiating tumor recurrence from treatment effect (radiation necrosis or pseudoprogression) in patients previously treated with chemo-radiation therapy for primary high grade gliomas. This will be accomplished by examining the concordance between the Dynamic PET imaging prediction and the criterion standard, which will be based on either surgical pathology or an integrated clinical/MRI determination within a 3-6 month interval after Dynamic PET imaging.

SECONDARY OBJECTIVES:

I. The diagnostic accuracy of Static PET imaging, advanced MRI, and advanced MRI + Dynamic PET imaging in differentiating tumor recurrence from radiation-induced necrosis in high grade glioma patients will be examined in the same exact way as just outlined for Dynamic PET imaging.

OUTLINE:

Subjects receive 18FDG (first scan) and (18)F-FDOPA (2-14 days from the first scan) intravenously (IV) slowly over a period of 15-20 seconds and then undergo dynamic PET scans over a period of 60-90 minutes. CT scans on the subjects are performed before the dynamic PET scans for 5 minutes. Subjects also undergo MRI brain examinations just prior to the FDOPA scan over a period of 1 hour, which includes T1 weighed, T1 weighted contrast enhanced, T2 weighted, Diffusion tensor imaging, MR spectroscopy, and Dynamic susceptibility contrast perfusion weighted (DSC-PWI) imaging.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 5
• Est. completion date: June 20, 2024
• Est. primary completion date: December 20, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age > 18

• Known or suspected recurrent malignant brain tumors

• Radiographic worsening reported on MRI shortly (within 3 months) after completion of radiation and temozolomide therapy

• Able to lie flat and/or still for a minimum of 60 minutes

• Willingness and ability to comply with scheduled visits and study procedures

• Patients who have a clinical indication for a PET-CT

• If female, patient must be postmenopausal or surgically sterile

Exclusion Criteria:

• Conditions that preclude a clinical brain FDG PET study, including: Consumption of liquids with sugar and/or caffeine prior to the study, Blood glucose levels over 150 mg/mL, Eating or drinking calories of any type within 4 hours of radiotracer injection, Hyperinsulinemia, Patients who for any reason cannot tolerate lying supine for 60 minutes

• Conditions that preclude a FDOPA PET study, including: Consuming a diet that is NOT low in protein after the previous evening meal

• Tumor located in the striatum

• Changes in medication (new prescriptions or change in dosages) between visits 1 and 2

• Pregnant, nursing, or lactating

• Women of childbearing potential (premenopausal female capable of becoming pregnant), which also includes:

women on oral, injectable, or mechanical contraceptives, women who are single, women whose male partners have been vasectomized or whose male partners have received or are utilizing mechanical contraceptive devices

• Weight > 450 lbs

• Known allergic reactions to 3,4-dihydroxy-6-[18F]fluoro-L-phenylalanine (18F-FDOPA) and Fluorine-18 fluorodeoxyglucose (18F-FDG)

• Confirmation that study eligibility criteria have not been met between visits 1 and 2

Related Conditions & MeSH terms

• Glioblastoma

Intervention

Procedure:
• Positron Emission Tomography
Undergo PET/CT Scans
• Computed Tomography
Undergo PET/CT Scans
• Multiparametric Magnetic Resonance Imaging Scan
Undergo a multiparametric MRI scan

Radiation:
• Fludeoxyglucose F-18
IV (intravenous) administration of radiotracer
• fluorine F 18 fluorodopa
IV (intravenous) administration of radiotracer

Locations

Country	Name	City	State
United States	University of Virginia	Charlottesville	Virginia

Sponsors (1)

Lead Sponsor	Collaborator
University of Virginia

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quantitative parametric maps indicating differences in rates of glucose and amino acid uptake (Ki) obtained from dynamic FDG and FDOPA scans respectively.	Will be derived from PET/CT scan imaging.	Up to 6 months
Primary	Quantitative parametric maps indicating differences in details (d) components of the wavelet transform analysis, d6 and d8, based on established tumor feature criterions.	Will be derived from MRI brain scan imaging.	Up to 6 months
Primary	Semi-quantitative standardize uptake value (SUV) parametric maps based on static PET scans (last 20 minutes of the dynamic PET scans).	Will be derived from PET/CT scan imaging.	Up to 6 months
Primary	MRI brain metrics	Including anatomic assessment based on T1, T2, and contrast enhanced T1 weighted imaging, MR spectroscopy data (choline, creatinine, and N-acetyl acetate peak integrals and ratios), MR perfusion data (relative cerebral blood volume), and diffusion tensor imaging data (apparent diffusion coefficient, fractional anisotropy)	Up to 6 months
Primary	Surgical pathology or 3-6 month interval multidisciplinary clinical evaluation.	To be compared with the imaging analyses for comparing ability to differentiate tumor recurrence from radiation necrosis.	Up to 6 months