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Combined PSMA PET/MRI for Detection of Lymph Node Metastases in High-risk Prostate Cancer Patients

Primary Purpose

Prostatic Neoplasms, Neoplasm Metastasis

Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
PSMA-PET
PSMA-PET/MRI
PSMA-PET/CT
Sponsored by
Norwegian University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostatic Neoplasms focused on measuring Diagnostic imaging, Positron-emission tomography, Magnetic Resonance Imaging, Prostate-specific antigen, Lymph Nodes, PSMA, PET, Molecular imaging

Eligibility Criteria

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Inclusion criteria (surgery cohort):

  • High risk localized/locally advanced prostate cancer patients who are candidates for radical prostatectomy plus bilateral extended PLND; ISUP Gleason grade group ≥ 4

Inclusion criteria (radiotherapy cohort):

  • High-risk localized/locally advanced prostate cancer patients scheduled for radiation treatment of the prostate and pelvic lymph nodes; ISUP Gleason grade group ≥ 4

Exclusion criteria (surgery and radiotherapy cohort):

  • Prior history of any other cancer the last 5 years excluding basal cell carcinoma
  • Proven metastases in bones or other distant metastases
  • General contra-indications for MRI (pacemaker, aneurysm clips, any form of metal in the body, severe claustrophobia)
  • Serious concomitant systemic disorders that in the opinion of the investigator would compromise the patient's ability to complete the study or interfere with the evaluation of the efficacy and safety of the study objectives
  • Metal implants in the pelvic region which will deteriorate PET/MR/CT image quality.

Sites / Locations

  • Haukeland University HospitalRecruiting
  • University Hosptial of North NorwayRecruiting
  • St Olavs Hospital, Trondheim University HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

PSMA-PET/MRI and PET/CT for detection of lymph node metastases.

Arm Description

Each patients will undergo an MRI-, PET/MRI- and PET/CT-examination (on the same day) prior to treatment. Patients in the radiotherapy cohort will additionally undergo an MRI examination after hormonal treatment, before radiotherapy.

Outcomes

Primary Outcome Measures

Diagnostic accuracy of PSMA PET and combined PSMA PET/MRI
To compare the diagnostic accuracy of PSMA PET and combined PSMA PET/MRI to that of the current standard multiparametric MRI, using histopathology as the gold standard.

Secondary Outcome Measures

Sensitivity and specificity of PSMA PET/MRI
To evaluate the sensitivity and specificity of PSMA PET/MRI to detect positive lymph nodes in high-risk prostate cancer patients in a prospective, multicenter study.
Performance of PSMA PET/MRI versus PET/CT
Compare the performance of PET/MRI to PET/CT for detection of lymph node metastases

Full Information

First Posted
March 5, 2021
Last Updated
August 14, 2023
Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital, Haukeland University Hospital, University Hospital of North Norway
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1. Study Identification

Unique Protocol Identification Number
NCT04790968
Brief Title
Combined PSMA PET/MRI for Detection of Lymph Node Metastases in High-risk Prostate Cancer Patients
Official Title
Combined PSMA PET/MRI for Detection of Lymph Node Metastases in High-risk Prostate Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 28, 2021 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital, Haukeland University Hospital, University Hospital of North Norway

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
For high-risk prostate cancer patients, detection of lymph node metastases is crucial to ensure optimal treatment. Standard treatment for these patients is radiotherapy or surgery. The surgery involves resection of the prostate and the pelvic lymph nodes. Currently, the most reliable method to confirm lymph node metastases is by histologic examination of the resected lymph nodes. Ideally, one should be able to detect lymph node metastases prior to treatment. Then, the treatment could be better adjusted to each patient. Imaging methods such as prostate specific membrane antigen positron emission tomography (PSMA-PET) can possibly aid the detection of lymph node metastases. In this study, the investigators want to test whether PSMA-PET or a combination of PSMA-PET and MRI (magnetic resonance imaging) can improve staging of lymph nodes before treatment.
Detailed Description
High-risk prostate cancer patients have a high probability for lymph node metastases in the pelvic region. The lymph node status is an important prognostic factor in determining the risk of later relapses and a factor in treatment planning. Lymph node metastases outside the pelvis usually signify systemic treatment not amendable for curative treatment. High-risk prostate cancer patients are treated by radiotherapy or surgical resection of the prostate and the pelvic lymph nodes. Currently, the most reliable method for confirming lymph node metastases is by bilateral pelvic lymph node dissection during surgical treatment, and subsequent histologic examination. However, todays state-of-the art methods for the detection of lymph node metastases prior to treatment are clearly inadequate. Detection of lymph node metastases is crucial for determining whether the patient (i) is a candidate for localized treatment and, if so, (ii) optimizing the extent of the lymph node dissection / radiation field for localized treatment. Non-standard imaging methods such as prostate specific membrane antigen (PSMA)-PET-imaging have been shown to be able to aid in the detection of lymph node metastases. The purpose of this study is to test whether PSMA-PET or a combination of PSMA-PET and MRI can improve the sensitivity and specificity for pre-treatment lymph node staging in order to reduce both over- and undertreatment of high-risk prostate cancer patients. In this multi-centre study, at least 80 patients with high-grade prostate cancer (according to NCNN Guidelines, v 2.2022) will be examined with PSMA PET/MRI and PET/CT. Study recruitment will continue until 60 patients have received radial prostatectomy with extended pelvic lymph node dissection (ePLND) (surgery cohort) and 20 patients have been treated with radiotherapy to the prostate and pelvic lymph nodes (radiotherapy cohort). After the PET examinations, all patients will receive standard treatment and follow-up, which is determined by national guidelines and the patient's treating urologist and/or oncologist. Imaging data will be analyzed by radiologists and nuclear medicine physicians in collaboration. The imaging findings in the surgery cohort will be compared to the histology outcome after ePLND to assess the sensitivity and specificity for detection of lymph node involvement with PSMA PET/MRI. The data from the radiotherapy cohort will be used to assess the feasibility of PSMA PET/MRI-based radiotherapy planning. Advanced image processing and analysis methodology including the use of artificial intelligence will also be applied.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostatic Neoplasms, Neoplasm Metastasis
Keywords
Diagnostic imaging, Positron-emission tomography, Magnetic Resonance Imaging, Prostate-specific antigen, Lymph Nodes, PSMA, PET, Molecular imaging

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
PSMA-PET/MRI and PET/CT for detection of lymph node metastases.
Arm Type
Experimental
Arm Description
Each patients will undergo an MRI-, PET/MRI- and PET/CT-examination (on the same day) prior to treatment. Patients in the radiotherapy cohort will additionally undergo an MRI examination after hormonal treatment, before radiotherapy.
Intervention Type
Diagnostic Test
Intervention Name(s)
PSMA-PET
Intervention Description
Prostate specific membrane antigen positron emission tomography
Intervention Type
Diagnostic Test
Intervention Name(s)
PSMA-PET/MRI
Intervention Description
Prostate specific membrane antigen positron emission tomography combined with magnetic resonance imaging
Intervention Type
Diagnostic Test
Intervention Name(s)
PSMA-PET/CT
Intervention Description
Prostate specific membrane antigen positron emission tomography combined with computed tomography imaging
Primary Outcome Measure Information:
Title
Diagnostic accuracy of PSMA PET and combined PSMA PET/MRI
Description
To compare the diagnostic accuracy of PSMA PET and combined PSMA PET/MRI to that of the current standard multiparametric MRI, using histopathology as the gold standard.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Sensitivity and specificity of PSMA PET/MRI
Description
To evaluate the sensitivity and specificity of PSMA PET/MRI to detect positive lymph nodes in high-risk prostate cancer patients in a prospective, multicenter study.
Time Frame
1 month
Title
Performance of PSMA PET/MRI versus PET/CT
Description
Compare the performance of PET/MRI to PET/CT for detection of lymph node metastases
Time Frame
1 month

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria (surgery cohort): High risk localized/locally advanced prostate cancer patients who are candidates for radical prostatectomy plus bilateral extended PLND; ISUP Gleason grade group ≥ 4 Inclusion criteria (radiotherapy cohort): High-risk localized/locally advanced prostate cancer patients scheduled for radiation treatment of the prostate and pelvic lymph nodes; ISUP Gleason grade group ≥ 4 Exclusion criteria (surgery and radiotherapy cohort): Prior history of any other cancer the last 5 years excluding basal cell carcinoma Proven metastases in bones or other distant metastases General contra-indications for MRI (pacemaker, aneurysm clips, any form of metal in the body, severe claustrophobia) Serious concomitant systemic disorders that in the opinion of the investigator would compromise the patient's ability to complete the study or interfere with the evaluation of the efficacy and safety of the study objectives Metal implants in the pelvic region which will deteriorate PET/MR/CT image quality.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tone Frost Bathen, prof
Phone
95021097
Ext
0047
Email
tone.f.bathen@ntnu.no
First Name & Middle Initial & Last Name or Official Title & Degree
Ingerid Skjei Knudtsen, PhD
Phone
47393211
Ext
0047
Email
ingerid.s.knudtsen@ntnu.no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Øystein Risa, Prof
Organizational Affiliation
Norwegian University of Science and Technology, NTNU
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Morten Troøyen, MD
Organizational Affiliation
St. Olavs Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Haukeland University Hospital
City
Bergen
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alfred Honoré, MD, PhD
Phone
94282796
Ext
0047
Email
alfred.honore@helse-bergen.no
First Name & Middle Initial & Last Name & Degree
Kristina Førde
Phone
55974723
Ext
0047
Email
kristina.forde@helse-bergen.no
Facility Name
University Hosptial of North Norway
City
Tromsø
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hege S Haugnes, MD, PhD
Phone
99277080
Ext
0047
Email
hege.sagstuen.haugnes@unn.no
Facility Name
St Olavs Hospital, Trondheim University Hospital
City
Trondheim
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Torgrim Tandstad, MD, PhD
Phone
72826166
Ext
0047
Email
torgrim.tandstad@stolav.no

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Combined PSMA PET/MRI for Detection of Lymph Node Metastases in High-risk Prostate Cancer Patients

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