Utility of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging
Primary Purpose
Prostate Cancer
Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Hyperpolarized 13C-Pyruvate
Sponsored by
About this trial
This is an interventional treatment trial for Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- Age greater than 40 and less than 80 years
Clinical suspicion or history of prostate cancer reflected by one of the following:
- PSA > 4ng/ml
- Abnormal DRE exam
- Known tissue diagnosis of prostate cancer from prior workup
- Patient planning to undergo either a MRI targeted biopsy or radical prostatectomy for prostate cancer workup or treatment
Exclusion Criteria:
- Inability to undergo MRI scan
- Inability to receive IV contrast as per institutional protocol.
Sites / Locations
- University of Maryland Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Single-arm study in patients who are suspected or known to have prostate cancer
Arm Description
Perform metabolic magnetic resonance imaging on men suspected to have a prostate cancer to understand if metabolic MRI can be safely performed on this population
Outcomes
Primary Outcome Measures
CTCAE v4.0 higher than grade 2
Quantify the number of participants who get this scan and have treatment-related adverse events as assessed by CTCAE v4.0 higher than grade 2. Determine the number of participants who successfully complete a scan which meets a minimum quality standard as measured by signal to noise ratio on the scan.
hyperpolarized metabolic MRI in the diagnosis of prostate cancer.
Secondary Outcome Measures
Accuracy of metabolic MRI to diagnose prostate cancer
To study the accuracy of hyperpolarized metabolic MRI to diagnose prostate cancer. Compare the prediction of cancer from the MRI scan compared to actual diagnosis of cancer by any subsequent workup or procedure the participant undergoes. Prediction of cancer from MRI scan will be performed by assigning a standardized score (PIRADS v2.0). Actual diagnosis of cancer will be based on tissue pathology (with cancer grade characterized using the prostate cancer ISUP Grade Group system) from any procedure the patient undergoes.
Utility of metabolic MRI over standard MRI imaging in the diagnosis of prostate cancer
To examine the added utility of metabolic MRI over standard MRI imaging. Quantify the number of participants in which the MRI provided extra information that otherwise was not available during the course of the patient's workup.
Correlative metabolic analysis of tissue metabolite concentrations versus cancer diagnosis
To perform correlative metabolic analysis related to cancer diagnosis. Using the research tissue when it is available. Analyze tumor samples when available from participants and characterize the metabolite concentration (microgram/mg of tissue) within the tumor to determine how the concentration value compares to two outcomes of interest: 1: the numerical suspicion score (PIRADS v2.0 system) from the imaging from the patient and 2: The presence of cancer and grade of cancer (ISUP Grade Group system), when present, from pathology analysis performed on the tissue from the patient available. Analyze tumor samples when available from participants and characterize the metabolite concentration within the tumor to determine how this compares to the information from the imaging from the patient and pathology analysis performed on the tissue
Full Information
NCT ID
NCT04698564
First Posted
October 1, 2020
Last Updated
October 19, 2023
Sponsor
University of Maryland, Baltimore
1. Study Identification
Unique Protocol Identification Number
NCT04698564
Brief Title
Utility of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging
Official Title
Utility of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging in the Diagnosis and Risk-Stratification of Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
February 1, 2025 (Anticipated)
Study Completion Date
February 1, 2027 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Maryland, Baltimore
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a two-tiered pilot study in which there will be no randomization and no placebo treatment. This study will be to perform metabolic magnetic resonance imaging on men suspected to have a prostate cancer to understand if metabolic MRI can be safely performed on this population
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Single-arm study in patients who are suspected or known to have prostate cancer
Arm Type
Experimental
Arm Description
Perform metabolic magnetic resonance imaging on men suspected to have a prostate cancer to understand if metabolic MRI can be safely performed on this population
Intervention Type
Drug
Intervention Name(s)
Hyperpolarized 13C-Pyruvate
Intervention Description
Hyperpolarized Pyruvate (13C) Injection, containing spin-polarized ("hyperpolarized") [ 13C]pyruvate, is being studied as a diagnostic agent in combination with 13C spectroscopic MR imaging. The aim is to visualize [13C]pyruvate and its metabolites and thereby distinguish between anatomical areas with normal vs. abnormal metabolism, which should be useful in diagnosing and characterizing, for example, malignancy.
Hyperpolarized Pyruvate (13C) Injection and [13C]pyruvate are general terms used throughout this brochure, that refer to all 13C labeling patterns, such as [1- 13C]pyruvate, [2- 13C]pyruvate and [1,2- 13C]pyruvate. From biological and safety standpoints, pyruvate with each of the labeling patterns behaves identically in the human body [Koletzko et al., 1997].
Primary Outcome Measure Information:
Title
CTCAE v4.0 higher than grade 2
Description
Quantify the number of participants who get this scan and have treatment-related adverse events as assessed by CTCAE v4.0 higher than grade 2. Determine the number of participants who successfully complete a scan which meets a minimum quality standard as measured by signal to noise ratio on the scan.
hyperpolarized metabolic MRI in the diagnosis of prostate cancer.
Time Frame
Within three years post treatment
Secondary Outcome Measure Information:
Title
Accuracy of metabolic MRI to diagnose prostate cancer
Description
To study the accuracy of hyperpolarized metabolic MRI to diagnose prostate cancer. Compare the prediction of cancer from the MRI scan compared to actual diagnosis of cancer by any subsequent workup or procedure the participant undergoes. Prediction of cancer from MRI scan will be performed by assigning a standardized score (PIRADS v2.0). Actual diagnosis of cancer will be based on tissue pathology (with cancer grade characterized using the prostate cancer ISUP Grade Group system) from any procedure the patient undergoes.
Time Frame
Within three years post treatment
Title
Utility of metabolic MRI over standard MRI imaging in the diagnosis of prostate cancer
Description
To examine the added utility of metabolic MRI over standard MRI imaging. Quantify the number of participants in which the MRI provided extra information that otherwise was not available during the course of the patient's workup.
Time Frame
Within three years post treatment
Title
Correlative metabolic analysis of tissue metabolite concentrations versus cancer diagnosis
Description
To perform correlative metabolic analysis related to cancer diagnosis. Using the research tissue when it is available. Analyze tumor samples when available from participants and characterize the metabolite concentration (microgram/mg of tissue) within the tumor to determine how the concentration value compares to two outcomes of interest: 1: the numerical suspicion score (PIRADS v2.0 system) from the imaging from the patient and 2: The presence of cancer and grade of cancer (ISUP Grade Group system), when present, from pathology analysis performed on the tissue from the patient available. Analyze tumor samples when available from participants and characterize the metabolite concentration within the tumor to determine how this compares to the information from the imaging from the patient and pathology analysis performed on the tissue
Time Frame
Within three years post treatment
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than 40 and less than 80 years
Clinical suspicion or history of prostate cancer reflected by one of the following:
PSA > 4ng/ml
Abnormal DRE exam
Known tissue diagnosis of prostate cancer from prior workup
Patient planning to undergo either a MRI targeted biopsy or radical prostatectomy for prostate cancer workup or treatment
Exclusion Criteria:
Inability to undergo MRI scan
Inability to receive IV contrast as per institutional protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Minhaj Siddiqui, MD
Phone
617-939-4823
Email
msiddiqui@som.umaryland.edu
Facility Information:
Facility Name
University of Maryland Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohummad Siddiqui, MD
12. IPD Sharing Statement
Learn more about this trial
Utility of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging
We'll reach out to this number within 24 hrs