Imaging Properties of PET Radiotracer [18F]3F-PHPG in Patients With Neuroendocrine Tumors
Study Details
Study Description
Brief Summary
The goal of this exploratory study is to test whether [18F]3F-PHPG can be used reliably to map the locations of tumors in patients with neuroendocrine tumors. If so, the results of this study will be used to support further development of [18F]3F-PHPG as a clinical tool for neuroendocrine tumor localization and staging.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Early Phase 1 |
Detailed Description
Subjects enrolled in this study will be recruited from the population of adult patients with neuroendocrine tumors, including pheochromocytoma and paraganglioma, being treated at the University of Michigan Hospital.
The primary objective of the study is to obtain basic information on the biodistribution and pharmacokinetics of [18F]3F-PHPG in cancer patients with neuroendocrine tumors.
The secondary objective of the study is to compare the diagnostic performance of [18F]3F-PHPG in cancer patients with neuroendocrine tumors with the FDA approved radiopharmaceuticals [123I]metaiodobenzylguanidine ([123I]MIBG) and [68Ga]DOTA-TATE in the same patients. A group of approximately 12 of the subjects scanned with [18F]3F-PHPG will be recruited to undergo a whole-body [123I]MIBG scan using planar scintigraphy with a gamma camera, following the standard clinical protocol used at the University of Michigan. In addition, a single SPECT/CT scan of the primary neuroendocrine tumor will be acquired after the whole-body scan to provide a tomographic image for comparison with the positron emission tomography (PET) image acquired using [18F]3F-PHPG. Several subjects enrolled on this study will undergo [68Ga]DOTA-TATE scans off-study, as part of routine clinical management. Existing [68Ga]DOTA-TATE scans will be obtained from consenting subjects' medical records.
This is an exploratory study and thus all statistical data analyses will be exploratory in nature.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: PET/CT scan with radiotracer [18F]3F-PHPG Novel radiotracer [18F]3F-PHPG prior to whole-body PET/CT scan. |
Drug: 3-[18F]Fluoro-para-hydroxyphenethylguanidine
Single IV injection of 12.0 mCi (+/- 10%) [18F]3F-PHPG
Other Names:
Diagnostic Test: Positron emission tomography/computed tomography scan
Whole-body PET/CT scan performed at two time-points: 1.5 hours and 3 hours after IV injection of [18F]3F-PHPG
Other Names:
|
| Active Comparator: Planar scintigraphy/SPECT scans with radiotracer [123I]MIBG FDA approved radiotracer [123I]MIBG prior to whole-body planar scintigraphy and SPECT/CT scan (standard clinical imaging procedures). |
Drug: 3-[18F]Fluoro-para-hydroxyphenethylguanidine
Single IV injection of 12.0 mCi (+/- 10%) [18F]3F-PHPG
Other Names:
Drug: [123I] metaiodobenzylguanidine
Single IV injection of 10.0 mCi [123I]MIBG
Other Names:
Diagnostic Test: Positron emission tomography/computed tomography scan
Whole-body PET/CT scan performed at two time-points: 1.5 hours and 3 hours after IV injection of [18F]3F-PHPG
Other Names:
Diagnostic Test: Planar scintigraphy scan
Whole-body scan using planar scintigraphy with a gamma camera performed the day after IV injection of [123I]MIBG
Diagnostic Test: Single photon emission computed tomography/computed tomography scan
SPECT/CT scan of the primary neuroendocrine tumor performed the day after IV injection of [123I]MIBG
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Image quality assessed by standardized uptake values [Up to 180 minutes]
The maximum standardized uptake value (SUVmax) of [18F]3F-PHPG in neoplastic lesions will be quantified from the PET images using region-of-interest (ROI) analysis.
- Biodistribution of [18F]3F-PHPG [90 minutes and 180 minutes after administration of tracer]
Changes in the measured tissue concentrations (kBq/cc) of [18F]3F-PHPG in neoplastic lesions and abdominal organs from the two acquired PET images (acquired at 90 min and 180 min after tracer injection).
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Current neuroendocrine tumor diagnosis
-
Able to lie flat for 60 minutes
-
Provision of informed consent
Exclusion Criteria:
-
Pregnancy or lactation
-
Claustrophobia
-
Inability to lie flat for 60 minutes
-
Currently taking medications that may alter PET scans of neuroendocrine tumors with these tracers, including any of the following:
-
Tricyclic antidepressants, which inhibit the norepinephrine transporter: desipramine, amitriptyline, imipramine
-
Cold medications containing the sympathomimetic amines: phenylephrine, phenylpropanolamine, pseudoephedrine
-
Nasal decongestants (some use phenylephrine as the active agent)
-
Cocaine (which inhibits the norepinephrine transporter)
-
Tetrabenazine (Xenazine), which inhibits the VMAT2 transporter
-
Monoamine oxidase inhibitors (MAOI)
-
Some antihypertensive drugs: reserpine, labetalol, α-methyldopa, clonidine
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Michigan Rogel Cancer Center | Ann Arbor | Michigan | United States | 48109 |
Sponsors and Collaborators
- University of Michigan Rogel Cancer Center
Investigators
- Principal Investigator: David Raffel, Ph.D., University of Michigan Rogel Cancer Center
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- UMCC 2019.174
- HUM00167104
- UM-FHPG-03