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Clinical Trials/NCT02678351
NCT02678351
Completed
Phase 2

68Ga-PSMA-11 PET/MRI for Detection of Regional Nodal and Distant Metastases in Patients With Intermediate and High-Risk Prostate Cancer

Andrei Iagaru1 site in 1 country74 target enrollmentApril 18, 2016

Overview

Phase
Phase 2
Intervention
68Ga-PSMA-11
Conditions
Stage II Prostate Adenocarcinoma
Sponsor
Andrei Iagaru
Enrollment
74
Locations
1
Primary Endpoint
68Ga-PSMA-11 PET Detection of Prostate Cancer Metastasized to Lymph Nodes
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This phase 2-3 trial studies the utility of 68-gallium (68Ga)-prostate-specific membrane antigen 11 (PSMA-11) positron emission tomography/magnetic resonance imaging (PET/MRI) to find tumors in patients with prostate cancer who are undergoing resection surgery for prostate cancer that is prognostically expected to spread quickly (intermediate-risk) or is likely to come back or spread (high-risk). Diagnostic procedures, such as PET/MRI, may help find and diagnose prostate cancer, and reveal out how far the disease has spread. Radioactive drugs, such as 68Ga-PSMA-11, may bind to tumor cells that have specific receptors, and may allow doctors to see smaller tumors than the standard of care contrast-enhanced computed tomography (CT) or MRI scan.

Detailed Description

OBJECTIVES: 1. To evaluate 68Ga-PSMA-11 PET/MRI for detection of tumor metastases in patients with intermediate and high-risk prostate cancer scheduled to undergo prostatectomy with lymph node dissection. 2. To assess sensitivity (positive predictive value) and specificity (negative predictive value) of 68Ga-PSMA-11 PET/MRI for the detection of regional nodal metastases compared to pathology at radical prostatectomy. OUTLINE: Participants will receive 68Ga-PSMA-11 intravenously (IV). Patients then undergo PET/MRI after 45 minutes of administration of radiopharmaceutical injection. After completion of study, patients are followed up at 24 to 48 hours.

Registry
clinicaltrials.gov
Start Date
April 18, 2016
End Date
December 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Andrei Iagaru

Associate Professor of Radiology

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

68Ga-PSMA PET/MRI

Patients receive 68Ga-PSMA-11 IV. Patients then undergo PET/MRI after 45 minutes of administration of radiopharmaceutical injection.

Intervention: 68Ga-PSMA-11

68Ga-PSMA PET/MRI

Patients receive 68Ga-PSMA-11 IV. Patients then undergo PET/MRI after 45 minutes of administration of radiopharmaceutical injection.

Intervention: Magnetic resonance imaging (MRI)

68Ga-PSMA PET/MRI

Patients receive 68Ga-PSMA-11 IV. Patients then undergo PET/MRI after 45 minutes of administration of radiopharmaceutical injection.

Intervention: Positron Emission Tomography (PET)

Outcomes

Primary Outcomes

68Ga-PSMA-11 PET Detection of Prostate Cancer Metastasized to Lymph Nodes

Time Frame: 1 Day

68-gallium (68Ga)-prostate-specific membrane antigen (PSMA) positron emission tomography/magnetic resonance imaging (PET/MRI) will be used to detect regional nodal and distant metastases in participants with intermediate and high-risk prostate cancer scheduled to undergo prostatectomy with lymph node dissection. The data will be analyzed by imaging interpretation. Each participant will be interpreted as either positive or negative for the presence of metastatic disease by 68Ga-PSMA PET/MRI, as assessed by imaging interpretation. The outcome will be expressed as the number of participants with metastatic disease, as identified by PET/MRI, a number without dispersion.

Secondary Outcomes

  • Histopathologic Detection of Prostate Cancer Metastasized to Lymph Nodes(1 Day)
  • Sensitivity of 68Ga-PSMA-11 PET/MRI(1 Day)
  • Specificity of 68Ga-PSMA-11 PET/MRI(1 Day)

Study Sites (1)

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