SUV on PSMA PET/CT in Non-Prostate Tumors

Sponsor
Sir Mortimer B. Davis - Jewish General Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT03841760
Collaborator
(none)
150
1
1
70.2
2.1

Study Details

Study Description

Brief Summary

The objective of this pilot study is to evaluate if 18F-DCFPyL PET/CT or 68Ga-PSMA-11 PET/CT can be used for detection and staging of PSMA-expressing non-prostate tumor.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: PSMA PET/CT
Phase 2

Detailed Description

Prostate specific membrane antigen (PSMA) is a unique membrane bound glycoprotein, which is over-expressed many fold on prostate cancer cells and other types of cancer. Since PSMA is a new target for molecular therapy, PSMA PET/CT allows assessment for therapy in addition to characterization of tumors and staging. Given the success of PSMA PET/CT for prostate cancer and the increasing number of case reports on PSMA uptake in non-prostate cancer, the aim of this project is to fill this literature gap by documenting the avidity of tumors (by means of SUVmax) based on their PSMA immunostaining (by the pathologist) or based on literature report (peer-reviewed article confirming PSMA expression in a tumor type).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
SUV on PSMA PET/CT in Non-Prostate Tumors
Actual Study Start Date :
Jul 25, 2019
Anticipated Primary Completion Date :
Jun 1, 2025
Anticipated Study Completion Date :
Jun 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: PSMA PET/CT

One (1) PSMA PET/CT scan with with either PSMA-11 or DCFPyL

Diagnostic Test: PSMA PET/CT
For 18F-DCFPyL PET/CT: Approximately 9 mCi (333MBq) of 18F-DCFPyL is injected intravenously. Approximately 60-90 minutes following 18F-DCFPyL injection, CT and PET images are consecutively acquired from the base of the skull to the toes. For 68Ga-PSMA-11 PET/CT: Approximately 2.5 MBq/kg (0.068 mCi/kg) of 68Ga-PSMA, up to a maximum of 300 MBq (8 mCi), is injected intravenously. Approximately 60 minutes following 68Ga-PSMA injection, CT and PET images are consecutively acquired from the base of the skull to toes.
Other Names:
  • PSMA PET
  • Outcome Measures

    Primary Outcome Measures

    1. Confirm PSMA PET uptake in tumors studied [Immediate]

      1. To confirm 18F-DCFPyL PET/CT or 68Ga-PSMA-11 uptake in the known tumor or other lesions found on PSMA PET/CT. The threshold for a positive lesion is a semi-quantitative measurement of activity: SUVmax > 4 in lesions larger than 1.5 cm (so as to offset PET partial volume effect or "camera limitations"). IF SUVmax > 4, the tumor is positive for PSMA PET/CT; If not, the tumor is negative for PSMA PET/CT.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 120 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age 18 years or older, able to understand and provide written informed consent

    • The patient has a tumor known or suspected to have PSMA expression, as reported in the literature or by positive histopathological staining for PSMA.

    • The known or suspected tumor must fall into one of the following categories: carcinoma, sarcoma, or hematologic cancer.

    • ECOG performance status 0 - 3, inclusive

    • Under referring physician's care

    • Able to tolerate the physical/logistical requirements of a PET/CT scan including lying supine for up to 40 minutes with the arms above the head and tolerating intravenous cannulation

    Exclusion Criteria:
    • Patients with neoplasm known in literature to not have PSMA expression, unless patient specific tissue sampling shows PSMA staining on histopathology.

    • Medically unstable patients (e.g. acute cardiac or respiratory distress or hypotensive, etc.)

    • Patients who exceed the safe weight limit of the PET/CT bed (200 kg) or who cannot fit through the PET/CT bore (70 cm diameter)

    • Patients with unmanageable claustrophobia

    • Pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Jewish General Hospital Montreal Quebec Canada H3T1E2

    Sponsors and Collaborators

    • Sir Mortimer B. Davis - Jewish General Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Stephan Probst, MD, Chief of Nuclear Medicine, Sir Mortimer B. Davis - Jewish General Hospital
    ClinicalTrials.gov Identifier:
    NCT03841760
    Other Study ID Numbers:
    • 2019-1531
    First Posted:
    Feb 15, 2019
    Last Update Posted:
    Dec 13, 2021
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Dec 13, 2021