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Unfavorable MRI But Favorable 68Ga-PSMA PET/MRI for Primary Prostate Cancer Detection

Primary Purpose

Prostate Neoplasm

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
multiparametric MRI and 68Ga-PSMA PET/MRI
Prostate biopsy
Sponsored by
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Neoplasm

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Men more than 18 years old with clinical suspicion of prostate cancer;
  2. Serum prostate-specific antigen (PSA) > 4 ng/ml within the previous 3 months;
  3. PI-RADS score no more than 3 or normal mpMRI of prostate;
  4. Suspicious lesion(s) within prostate on 68Ga-PSMA PET/MRI;
  5. no evidence of PSA increase by noncancerous factors, such as catheterization, bladder stones, or urinary tract infection including bacterial prostatitis;
  6. Able to provide written informed consent.

Exclusion Criteria:

  1. Prior prostate biopsy or prostate surgery;
  2. Prior treatment for prostate cancer;
  3. Contraindication to MRI or PET (e.g. claustrophobia, pacemaker, estimated glomerular filtration rate ≤ 50mls/min);
  4. Contraindication to prostate biopsy.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Prostate biopsy with 68Ga-PSMA PET/MRI

    Arm Description

    Both targeted biopsy and 12-core systematic biopsy with positive 68Ga-PSMA PET/MRI

    Outcomes

    Primary Outcome Measures

    Detection rate of prostate cancer
    Detection rate of prostate cancer

    Secondary Outcome Measures

    Detection rates of clinically significant PCa and clinically insignificant prostate cancer
    Detection rates of clinically significant PCa and clinically insignificant prostate cancer
    Gleason grade group distribution (score from 1 to 5, the bigger the score, the worse the prognosis) and aggressive architecture (such as cribriform) on final pathology
    Gleason grade group distribution (score from 1 to 5, the bigger the score, the worse the prognosis) and aggressive architecture (such as cribriform) on final pathology
    Optimal cut-off uptake value on PET/MRI for prostate cancer detection
    Optimal cut-off uptake value on PET/MRI for prostate cancer detection

    Full Information

    First Posted
    October 10, 2019
    Last Updated
    October 10, 2019
    Sponsor
    The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04124107
    Brief Title
    Unfavorable MRI But Favorable 68Ga-PSMA PET/MRI for Primary Prostate Cancer Detection
    Official Title
    Diagnostic Performance of 68Ga-PSMA PET/MRI in Suspicious Biopsy-naive Prostate Cancer Patients With Favorable Lesion on PET But Unfavorable on MRI for Primary Prostate Cancer Detection: a Pilot Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 2019 (Anticipated)
    Primary Completion Date
    November 2020 (Anticipated)
    Study Completion Date
    December 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This perspective cohort study aims to assess the detection rate of prostate cancer through prostate biopsy within suspicious patients harboring unfavorable multiparametric MRI but favorable 68Ga-PSMA PET/MRI who have had no prior prostate biopsy.
    Detailed Description
    Multiparametric MRI (MpMRI) is currently regarded as the best imaging method to noninvasively identify and characterize prostate cancer (PCa) with the Prostate Imaging Reporting and Data System (PI-RADS) v2. However, there are diagnostic difficulties for suspicious patients with PI-RADS score 3 and not all PCa are equivalently visible on mpMRI. For such patients, other alternative imaging techniques are required to properly characterize and detect PCa. It has been widely reported that 68Ga-PSMA PET imaging offers excellent performance in detecting primary PCa and is able to noninvasively characterize the aggressiveness of PCa. Recently, integrated PET/MRI, which combines the strengths of both modalities, has been shown to have great potential for influencing clinical practice by providing a more certain map of localized PCa to aid targeted biopsies and therapy. This perspective cohort study aims to assess the detection rate of PCa through prostate biopsy within suspicious patients harboring unfavorable mpMRI but favorable 68Ga-PSMA PET/MRI who have had no prior prostate biopsy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Prostate Neoplasm

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    50 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Prostate biopsy with 68Ga-PSMA PET/MRI
    Arm Type
    Experimental
    Arm Description
    Both targeted biopsy and 12-core systematic biopsy with positive 68Ga-PSMA PET/MRI
    Intervention Type
    Device
    Intervention Name(s)
    multiparametric MRI and 68Ga-PSMA PET/MRI
    Intervention Description
    All participants will undergo multiparametric MRI examination. If mpMRI is unfavorable for prostate cancer, participants will undergo 68Ga-PSMA PET/MRI examination
    Intervention Type
    Procedure
    Intervention Name(s)
    Prostate biopsy
    Intervention Description
    Participants with unfavorable mpMRI but favorable 68Ga-PSMA PET/MRI will undergo both 68Ga-PSMA PET/MRI-ultrasound-fusion targeted biopsy and transperineal ultrasound guided 12-core systematic biopsy
    Primary Outcome Measure Information:
    Title
    Detection rate of prostate cancer
    Description
    Detection rate of prostate cancer
    Time Frame
    30 days post biopsy
    Secondary Outcome Measure Information:
    Title
    Detection rates of clinically significant PCa and clinically insignificant prostate cancer
    Description
    Detection rates of clinically significant PCa and clinically insignificant prostate cancer
    Time Frame
    30 days post biopsy
    Title
    Gleason grade group distribution (score from 1 to 5, the bigger the score, the worse the prognosis) and aggressive architecture (such as cribriform) on final pathology
    Description
    Gleason grade group distribution (score from 1 to 5, the bigger the score, the worse the prognosis) and aggressive architecture (such as cribriform) on final pathology
    Time Frame
    90 days post biopsy
    Title
    Optimal cut-off uptake value on PET/MRI for prostate cancer detection
    Description
    Optimal cut-off uptake value on PET/MRI for prostate cancer detection
    Time Frame
    30 days post-biopsy

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Men more than 18 years old with clinical suspicion of prostate cancer; Serum prostate-specific antigen (PSA) > 4 ng/ml within the previous 3 months; PI-RADS score no more than 3 or normal mpMRI of prostate; Suspicious lesion(s) within prostate on 68Ga-PSMA PET/MRI; no evidence of PSA increase by noncancerous factors, such as catheterization, bladder stones, or urinary tract infection including bacterial prostatitis; Able to provide written informed consent. Exclusion Criteria: Prior prostate biopsy or prostate surgery; Prior treatment for prostate cancer; Contraindication to MRI or PET (e.g. claustrophobia, pacemaker, estimated glomerular filtration rate ≤ 50mls/min); Contraindication to prostate biopsy.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Hongqian Guo, PhD
    Phone
    8613605171690
    Ext
    8613605171690
    Email
    dr.ghq@nju.edu.cn
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jie Gao, Bachelor
    Phone
    8613951784909
    Ext
    8613605171690
    Email
    medgaojie@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Hongqian Guo, PhD
    Organizational Affiliation
    The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
    Official's Role
    Study Chair

    12. IPD Sharing Statement

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    Unfavorable MRI But Favorable 68Ga-PSMA PET/MRI for Primary Prostate Cancer Detection

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