An Investigational Scan (18F-rhPSMA-7.3 PET-mpMRI) for Targeted Prostate Biopsy Using TRUS-MR Fusion Technique

Purpose

This phase II trial evaluates an imaging technique called 18F-rhPSMA-7.3 positron emission tomography (PET)-multiparametric (mp) magnetic resonance imaging (MRI) in identifying tumor tissue in men suspected to have prostate cancer. This clinical trial also seeks to determine if the abnormal tissue identified during imaging represents the tumor tissue removed during transrectal ultrasound-magnetic resonance imaging (TRUS-MR) fusion biopsy of the prostate. PET is an established imaging technique that utilizes small amounts of radioactivity attached to very minimal amounts of tracer, in the case of this research, 18F-rhPSMA-7.3. Because some tumors take up 18F-rhPSMA-7.3 it can be seen with PET. MRI uses radio waves and a powerful magnet linked to a computer to create detailed pictures of areas inside the body. These pictures can show the difference between normal and diseased tissue. Standard of care imaging for prostate cancer includes mpMRI, which is the combination of multiple magnetic resonance techniques, including diffusion weighted imaging, dynamic contrast-enhanced imaging, and spectroscopy, to achieve an image that will allow for better identification of tumor size and location, as well as possibly identifying tumor spread and aggressiveness. However, mpMRI may not be as effective in identifying prostate tumors that are clinically significant. A TRUS-MR biopsy involves using both ultrasound and MRI scans to locate abnormal areas in the prostate. An 18F-rhPSMA-7.3 PET-mpMRI may be more effective than mpMRI alone in identifying tumor tissue and may increase the accuracy of TRUS-MRI fusion biopsies in men suspected of having prostate cancer.

Condition

  • Prostate Carcinoma

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male subjects aged > 18 years - Patients with suspected prostate cancer who will have prostate biopsy for confirmation - Ability to lie still for MRI scanning - Patients must be able to provide written informed consent

Exclusion Criteria

  • Documented acute prostatitis, symptomatic or severe benign prostatic hyperplasia (BPH) or urinary tract infections - Patients with contraindications for MRI including implantable pace makers, cochlear implants - Patients with uni- or bilateral hip prosthesis - Subjects with other significant medical conditions that would create unacceptable prostate biopsy risk, compromise retention on study or compromise study related assessments - Prostate biopsy within 4 weeks prior to entry on this study in which inflammation might affect PET-mpMR result - Is determined by the Investigator that the patient is clinically unsuitable for the study - Is incapable of understanding the language in which the information for the patient is given - Participation in a concurrent clinical trial or in another trial within the past 30 days

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Diagnostic
Masking
None (Open Label)
Masking Description
MR interpreters will be blinded to PET findings

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Diagnostic (18F-rhPSMA-7.3 PET, mpMRI, TRUS-MR fusion biopsy) 		Patients receive 18F-rhPSMA-7.3 IV and, 50 minutes later, undergo PET over 30 minutes at the time of SOC mpMRI. Patients may also undergo standard of care TRUS-MR fusion biopsy of targets identified on SOC mpMRI.
  • Drug: Flotufolastat F-18 Gallium
    Given IV
    Other names:
    • (18F)-rhPSMA-7.3
    • 18F-rhPSMA-7.3
    • 18FrhPSMA-7.3
    • F-18-rhPSMA-7.3
    • Fluorine F 18 Radiohybrid PSMA-7.3
    • Fluorine F 18 rhPSMA-7.3
    • Fluorine-18 rhPSMA-7.3
    • Posluma
    • rhPSMA-7.3 (18F)
  • Procedure: Magnetic Resonance Imaging
    Undergo TRUS-MR fusion biopsy
    Other names:
    • Magnetic Resonance
    • Magnetic Resonance Imaging (MRI)
    • Magnetic resonance imaging (procedure)
    • Magnetic Resonance Imaging Scan
    • Medical Imaging, Magnetic Resonance / Nuclear Magnetic Resonance
    • MR
    • MR Imaging
    • MRI
    • MRI Scan
    • MRIs
    • NMR Imaging
    • NMRI
    • Nuclear Magnetic Resonance Imaging
    • sMRI
    • Structural MRI
  • Procedure: Multiparametric Magnetic Resonance Imaging
    Undergo mpMRI
    Other names:
    • MP-MRI
    • mpMRI
    • Multi-parametric MRI
    • Multiparametric MRI
  • Procedure: Positron Emission Tomography
    Undergo PET
    Other names:
    • Medical Imaging, Positron Emission Tomography
    • PET
    • PET Scan
    • Positron emission tomography (procedure)
    • Positron Emission Tomography Scan
    • Positron-Emission Tomography
    • PT
  • Procedure: Transrectal Ultrasonography Guided Biopsy
    Undergo TRUS-MR fusion biopsy
    Other names:
    • TRUS Biopsy
    • TRUS-Guided Biopsy

Recruiting Locations

Emory University Hospital
Atlanta, Georgia 30322
Contact:
Khushali M. Vashi
khushali.vashi@emory.edu

More Details

Status
Recruiting
Sponsor
Emory University

Study Contact

David M. Schuster, MD, FACR
404-712-4859
dschust@emory.edu

Detailed Description

PRIMARY OBJECTIVE: I. To determine if simultaneous flotufolastat F-18 gallium (18F-rhPSMA-7.3) PET-mpMR improves the detection of clinically significant prostate cancer (csPCa) in Prostate Imaging-Reporting and Data System (PI-RADS) ≥ 3 lesions. SECONDARY OBJECTIVE: I. To explore associations between radiomics textural data from the PET acquisition, mpMR imaging, or both with the presence of csPCa. OUTLINE: Patients receive 18F-rhPSMA-7.3 intravenously (IV) and, 50 minutes later, undergo PET over 30 minutes at the time of standard of care (SOC) mpMRI. Patients may also undergo standard of care TRUS-MR fusion biopsy of targets identified on SOC mpMRI.