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Mp-3TMRI and 68Ga-PSMA PET/CT Guided Prostate Biopsy and Tumor Node Metastasis (TNM) Staging. (BIOPSTAGE)

Primary Purpose

68Ga-PSMA PET/CT Guided Prostate Biopsy, Mp-3TMRI Guided Prostate Biopsy, Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
pelvic MRI
68Ga-PSMA PET/CT
Sponsored by
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for 68Ga-PSMA PET/CT Guided Prostate Biopsy focused on measuring Diagnosis Prostate Cancer, TNM staging, 68Ga-PSMA PET/CT guided prostate biopsy, mp-3TMRI guided prostate biopsy, pre-surgical staging, clinically-suspected prostate cancer

Eligibility Criteria

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

Inclusion Criteria:

Cohort 1 - Biopsy guidance in clinically-suspected PCa

1. Men aged 45 to 75 years old with clinically-suspected PCa candidated for either initial or repeat TRUS-guided prostate biopsy, meeting any of the following criteria:

a) Abnormal PSA metrics, defined as follows:

A rising and/or persistently elevated serum PSA (i.e PSA > 2.5ng/ml for men in the age group comprising 60 to 75 years old; PSA > 3.0ng/ml for men in the age group comprising 45 to 60 years old) and at least one of the following PSA-based metrics:

i. Percent free PSA (%fPSA) < 25% with PSA range 4-10ng/ml (NCCN); ii. PSA velocity (PSAvel) >0.35 ng/mL/y; iii. PSA density (PSAden) > 0.25ng/mL/cc iv. PSA > 10ng/ml, 50% risk of PCa (EAU) b) Suspicious digital rectal examination (DRE), 5-30% risk of PCa; c) Prostate Cancer Gene 3 (PCA3) > 35; d) Suspicious findings on first-round biopsy: i. A few Atypical Glands immediately adjacent to HG-PIN, 50% risk of PCa; ii. Atypical Small Acinar Proliferation, 40% of PCa; iii. Multifocal High-Grade Prostatic intraepithelial neoplasia (HG-PIN), 30% ; iv. Intraductal carcinoma as solitary finding, 90% of PCa;

Cohort 2 - Biopsy guidance on Active Surveillance

Men consenting to enter the PRIAS MRI side-study as per currently inclusion criteria in Version Number 1.0 dated August 20, 2013. These are:

  1. Histologically-proven adenocarcinoma of the prostate;
  2. Age ≥ 18
  3. Men should be fit for curative treatment;
  4. Clinical stage T1c or T2;
  5. Gleason score 3+3=6;
  6. One or two biopsy cores invaded with prostate cancer:

    1. If an MRI, including targeted biopsies on positive lesions, is done at inclusion, there is no limit in the number of positive cores (that is, more than two, and no limit in the % of cancer present in the cores);
    2. If saturation biopsies (either trans-perineal or trans-rectal) are done 15% of the cores can be positive with a maximum of 4 (i.e. 26 cores 4 cores can be positive) (all other inclusion criteria still apply);
  7. PSA density (PSA D) less than 0.2;
  8. PSA-level at diagnosis ≤ 10 ng/mL;

Cohort 3a - Pre-surgical TNM staging in high-risk prostate cancer

  1. Male, aged 18 years or older;
  2. Cyto / histological confirmation of PCa (i.e. TRUS-guided biopsies; TURP);
  3. Any of the PCa high risk features for Organ-Confined Disease (OCD):

    • Clinical T stage ≥ T2c;
    • Gleason Score ≥ 8;
    • Serum PSA > 20 ng/mL;
  4. Any of the PCa high-risk features for Locally-Advanced Disease (LAD):

    • Clinical T stage ≥ T3b-T4 OR any T and clinical N1 disease;
    • Gleason Score ≥ 8;
    • Serum PSA > 20 ng/mL;
  5. Routine clinical staging (CTscan ± Bone scan) performed within 12 weeks enrolment returning negative or equivocal results for distant metastatic disease;

Cohort 3b - pelvic TNM staging of prostate cancer prior to nerve-sparing radical prostatectomy

  1. Male, aged 18 years or older;
  2. Cyto / histological confirmation of PCa (i.e. TRUS-guided biopsies; TURP);
  3. All of the following PCa-related features must be met for nerve-sparing (either mono- or bi-lateral):

    • Clinical T stage ≤ T2b;
    • Gleason Score ≤ 7 (3+4) and maximum one biopsy with Gleason > 6 at the ipsilateral side;
    • Serum PSA < 10 ng/mL;

Exclusion Criteria:

The participant may not enter the study if ANY of the following apply:

  1. Hormone androgen deprivation therapy of any type within 6 months prior to enrollment.
  2. Prior pelvic radiotherapy;
  3. Sickle cell disease;
  4. Insufficient renal function (eGFR < 30 mL/min/1.73 m2);
  5. Hip prosthesis, vascular grafting or other conditions affecting imaging;
  6. Contraindication to MRI, including but not restricted to: pacemaker or other electronic im-plants, known metal in the orbit, MR incompatible surgical or cerebral aneurysm clips, shrapnel, tattoos, non-removable body piercings (relative contraindications);
  7. History of allergic reactions attributed to compounds of similar chemical or biologic com-position to 68Ga-PSMA or Gadolinium-based contrast agents used in the study.

Sites / Locations

  • AUSL della RomagnaRecruiting
  • Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Other

Other

Other

Arm Label

Cohort 1

Cohort 2

Cohort 3a

Cohort 3b

Arm Description

Men with suspected clinically-significant PCa (CS-PCa) who are candidates for prostate biopsy or after first-round negative transrectal ultrasonography (TRUS) biopsy

Men framed in Active Surveillance (PRIAS study), scheduled for PRIAS repeat biopsy.

Men with high-risk PCa (HR-PCa) prior to radical surgery.

Men diagnosed with CS-PCa prior to nerve-sparing prostate surgery (NSS).

Outcomes

Primary Outcome Measures

sensitivity of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
sensitivity of both 68Ga-PSMA PET/CT and mp-3TMRI imaging will be calculated as the ratio between the number of positive cases at 68Ga-PSMA PET/CT or mp-3TMRI and number of patients who underwent to these exams
specificity of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
specificity will be calculated considering negative cases at 68Ga-PSMA PET/CT or mp-3TMRI and number of patients who underwent to these exams
Positive predictive value of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
Positive predictive value will be calculated considering the ratio between positive patient at 68Ga-PSMA PET/CT/mp-3TMRI confirmed as positive throughout biopsy and overall positive patient at 68Ga-PSMA PET/CT/mp-3TMRI
negative predictive value of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
negative predictive value will be calculated considering the ratio between negative patient at 68Ga-PSMA PET/CT/mp-3TMRI confirmed as negative throughout biopsy and overall negative patient at 68Ga-PSMA PET/CT/mp-3TMRI

Secondary Outcome Measures

Incidence of adverse events
The number and percentage of treated patients undergoing grade 1 to 4 adverse events will be tabulated for each cohort and diagnostic procedure, using the National Cancer Institute's Common Terminology Criteria for Adverse Events (CTCAE) Version 4.03 should be used to assess and grade AE severity.

Full Information

First Posted
March 8, 2018
Last Updated
May 31, 2023
Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
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1. Study Identification

Unique Protocol Identification Number
NCT03465579
Brief Title
Mp-3TMRI and 68Ga-PSMA PET/CT Guided Prostate Biopsy and Tumor Node Metastasis (TNM) Staging.
Acronym
BIOPSTAGE
Official Title
Multi-cohort Investigational Study to Evaluate the Impact of Pelvic Mp-3TMRI and Whole-body 68Ga-PSMA PET/CT for Diagnosis of Clinically-significant Prostate Cancer and Pre-surgical Staging.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 23, 2018 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori

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
BIOPSTAGE is a prospective, non-randomized, diagnostic, multi-cohort investigational study to evaluate the impact of pelvic Multi-parametric 3-Tesla magnetic resonance imaging (mp-3TMRI) and whole-body 68Ga-PSMA PET/CT for diagnosis of clinically-significant prostate cancer and pre-surgical staging.
Detailed Description
The aim of this study is to characterize the diagnostic accuracy of both multi-parametric pelvic Magnetic Resonance Imaging (MRI) (T2-weighted, Diffusion Weighted Imaging (DWI), Dynamic Contrast Enhancement (DCE) and 68Ga-chelated Prostate Specific Membrane Antigen ligand (68Ga-PSMA) Positron Emission Tomography/Computed Tomography (PET /CT) in three cohorts of patients: COHORT 1 Guiding prostate biopsies in men with clinical suspicion and/or unconfirmed clinically-significant prostate cancer (CS-PCa) on initial prostate biopsy; COHORT 2 Targeting repeat prostate biopsy in patients on Active Surveillance (PRIAS Study), scheduled for PRIAS repeat biopsy; COHORT 3 Providing pelvic / whole-body pre-surgical staging in: 3a: men with high-risk PCa (HR-PCa); 3b: men candidates for nerve sparing surgery (NSS);

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
68Ga-PSMA PET/CT Guided Prostate Biopsy, Mp-3TMRI Guided Prostate Biopsy, Prostate Cancer, TNM Staging, Diagnosis
Keywords
Diagnosis Prostate Cancer, TNM staging, 68Ga-PSMA PET/CT guided prostate biopsy, mp-3TMRI guided prostate biopsy, pre-surgical staging, clinically-suspected prostate cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
306 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cohort 1
Arm Type
Other
Arm Description
Men with suspected clinically-significant PCa (CS-PCa) who are candidates for prostate biopsy or after first-round negative transrectal ultrasonography (TRUS) biopsy
Arm Title
Cohort 2
Arm Type
Other
Arm Description
Men framed in Active Surveillance (PRIAS study), scheduled for PRIAS repeat biopsy.
Arm Title
Cohort 3a
Arm Type
Other
Arm Description
Men with high-risk PCa (HR-PCa) prior to radical surgery.
Arm Title
Cohort 3b
Arm Type
Other
Arm Description
Men diagnosed with CS-PCa prior to nerve-sparing prostate surgery (NSS).
Intervention Type
Diagnostic Test
Intervention Name(s)
pelvic MRI
Intervention Description
multi-parametric pelvic MRI
Intervention Type
Diagnostic Test
Intervention Name(s)
68Ga-PSMA PET/CT
Intervention Description
68Ga-PSMA PET/CT
Primary Outcome Measure Information:
Title
sensitivity of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
Description
sensitivity of both 68Ga-PSMA PET/CT and mp-3TMRI imaging will be calculated as the ratio between the number of positive cases at 68Ga-PSMA PET/CT or mp-3TMRI and number of patients who underwent to these exams
Time Frame
up to 36 months
Title
specificity of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
Description
specificity will be calculated considering negative cases at 68Ga-PSMA PET/CT or mp-3TMRI and number of patients who underwent to these exams
Time Frame
up to 36 months
Title
Positive predictive value of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
Description
Positive predictive value will be calculated considering the ratio between positive patient at 68Ga-PSMA PET/CT/mp-3TMRI confirmed as positive throughout biopsy and overall positive patient at 68Ga-PSMA PET/CT/mp-3TMRI
Time Frame
up to 36 months
Title
negative predictive value of both 68Ga-PSMA PET/CT and mp-3TMRI imaging
Description
negative predictive value will be calculated considering the ratio between negative patient at 68Ga-PSMA PET/CT/mp-3TMRI confirmed as negative throughout biopsy and overall negative patient at 68Ga-PSMA PET/CT/mp-3TMRI
Time Frame
up to 36 months
Secondary Outcome Measure Information:
Title
Incidence of adverse events
Description
The number and percentage of treated patients undergoing grade 1 to 4 adverse events will be tabulated for each cohort and diagnostic procedure, using the National Cancer Institute's Common Terminology Criteria for Adverse Events (CTCAE) Version 4.03 should be used to assess and grade AE severity.
Time Frame
up to 30 days following study procedures

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cohort 1 - Biopsy guidance in clinically-suspected PCa 1. Men aged 45 to 75 years old with clinically-suspected PCa candidated for either initial or repeat TRUS-guided prostate biopsy, meeting any of the following criteria: a) Abnormal PSA metrics, defined as follows: A rising and/or persistently elevated serum PSA (i.e PSA > 2.5ng/ml for men in the age group comprising 60 to 75 years old; PSA > 3.0ng/ml for men in the age group comprising 45 to 60 years old) and at least one of the following PSA-based metrics: i. Percent free PSA (%fPSA) < 25% with PSA range 4-10ng/ml (NCCN); ii. PSA velocity (PSAvel) >0.35 ng/mL/y; iii. PSA density (PSAden) > 0.25ng/mL/cc iv. PSA > 10ng/ml, 50% risk of PCa (EAU) b) Suspicious digital rectal examination (DRE), 5-30% risk of PCa; c) Prostate Cancer Gene 3 (PCA3) > 35; d) Suspicious findings on first-round biopsy: i. A few Atypical Glands immediately adjacent to HG-PIN, 50% risk of PCa; ii. Atypical Small Acinar Proliferation, 40% of PCa; iii. Multifocal High-Grade Prostatic intraepithelial neoplasia (HG-PIN), 30% ; iv. Intraductal carcinoma as solitary finding, 90% of PCa; Cohort 2 - Biopsy guidance on Active Surveillance Men consenting to enter the PRIAS MRI side-study as per currently inclusion criteria in Version Number 1.0 dated August 20, 2013. These are: Histologically-proven adenocarcinoma of the prostate; Age ≥ 18 Men should be fit for curative treatment; Clinical stage T1c or T2; Gleason score 3+3=6; One or two biopsy cores invaded with prostate cancer: If an MRI, including targeted biopsies on positive lesions, is done at inclusion, there is no limit in the number of positive cores (that is, more than two, and no limit in the % of cancer present in the cores); If saturation biopsies (either trans-perineal or trans-rectal) are done 15% of the cores can be positive with a maximum of 4 (i.e. 26 cores 4 cores can be positive) (all other inclusion criteria still apply); PSA density (PSA D) less than 0.2; PSA-level at diagnosis ≤ 10 ng/mL; Cohort 3a - Pre-surgical TNM staging in high-risk prostate cancer Male, aged 18 years or older; Cyto / histological confirmation of PCa (i.e. TRUS-guided biopsies; TURP); Any of the PCa high risk features for Organ-Confined Disease (OCD): Clinical T stage ≥ T2c; Gleason Score ≥ 8; Serum PSA > 20 ng/mL; Any of the PCa high-risk features for Locally-Advanced Disease (LAD): Clinical T stage ≥ T3b-T4 OR any T and clinical N1 disease; Gleason Score ≥ 8; Serum PSA > 20 ng/mL; Routine clinical staging (CTscan ± Bone scan) performed within 12 weeks enrolment returning negative or equivocal results for distant metastatic disease; Cohort 3b - pelvic TNM staging of prostate cancer prior to nerve-sparing radical prostatectomy Male, aged 18 years or older; Cyto / histological confirmation of PCa (i.e. TRUS-guided biopsies; TURP); All of the following PCa-related features must be met for nerve-sparing (either mono- or bi-lateral): Clinical T stage ≤ T2b; Gleason Score ≤ 7 (3+4) and maximum one biopsy with Gleason > 6 at the ipsilateral side; Serum PSA < 10 ng/mL; Exclusion Criteria: The participant may not enter the study if ANY of the following apply: Hormone androgen deprivation therapy of any type within 6 months prior to enrollment. Prior pelvic radiotherapy; Sickle cell disease; Insufficient renal function (eGFR < 30 mL/min/1.73 m2); Hip prosthesis, vascular grafting or other conditions affecting imaging; Contraindication to MRI, including but not restricted to: pacemaker or other electronic im-plants, known metal in the orbit, MR incompatible surgical or cerebral aneurysm clips, shrapnel, tattoos, non-removable body piercings (relative contraindications); History of allergic reactions attributed to compounds of similar chemical or biologic com-position to 68Ga-PSMA or Gadolinium-based contrast agents used in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Oriana Nanni
Phone
+390543739266
Email
oriana.nanni@irst.emr.it
First Name & Middle Initial & Last Name or Official Title & Degree
Federica Matteucci, MD
Phone
+390543739100
Email
federica.matteucci@irst.emr.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Federica Matteucci
Organizational Affiliation
IRST IRCCS
Official's Role
Study Chair
Facility Information:
Facility Name
AUSL della Romagna
City
Forlì
State/Province
FC
ZIP/Postal Code
47121
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roberta Gunelli
Facility Name
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST)
City
Meldola
State/Province
FC
ZIP/Postal Code
47014
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Federica Matteucci, MD
Phone
+390543739100
Email
federica.matteucci@irst.emr.it

12. IPD Sharing Statement

Learn more about this trial

Mp-3TMRI and 68Ga-PSMA PET/CT Guided Prostate Biopsy and Tumor Node Metastasis (TNM) Staging.

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