Multi-modality Prostate Cancer Image Guided Interventions (IGPC-2)
Primary Purpose
Prostate Cancer
Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Imaging Panel
Sponsored by

About this trial
This is an interventional diagnostic trial for Prostate Cancer focused on measuring Prostate Cancer, PET/CT, PET/MRI, Fluorocholine, PSMA, Sodium (Na) MRI, [18-F]-FCH, [18-F]-DCFPyL, Hybrid imaging, Whole mount histopathology
Eligibility Criteria
Inclusion Criteria:
- Provision of informed consent for this study
- Male, aged 18 years or older
- Pathologically confirmed prostate cancer on previous biopsy
- Suitable for and consenting to Radical Prostatectomy for treatment, or repeat biopsy as standard of care
Exclusion Criteria:
- Prior therapy for prostate cancer (including hormone therapy), with the exception of radiation therapy for Cohort 2 only
- Use of 5-alpha reductase inhibitors, i.e. finasteride (Proscar) or dutasteride (Avodart) within 6 months of study start. Patients undergoing a 6-month washout period prior to study start will be eligible.
- Inability to comply with the pre-operative imaging panel
- Patients scheduled for radical prostatectomy with prostate size exceeding dimensions for whole mount pathology slides
- Allergy to contrast agents to be used as part of the imaging panel
- Sickle cell disease or other anemias
- Insufficient renal function (eGFR < 60 mL/min/1.73 m2)
- Residual bladder volume > 150 cc (determined by post-void ultrasound)
- Hip prosthesis, vascular grafting that is MRI incompatible or sources of artifact within the pelvis
Contraindication to MRI
- pacemaker or other electronic implants
- known metal in the orbit
- cerebral aneurysm clips
Sites / Locations
- London Health Sciences Centre
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Imaging Panel
Arm Description
Patients who provided written informed consent and found to be eligible for study were asked to complete Positron Emission Tomography (PET) + Dynamic CT imaging, PET/MRI (with endorectal coil) and 3D-Transrectal ultrasound prior to standard of care radical prostatectomy.
Outcomes
Primary Outcome Measures
Hybrid Imaging Map (HIM) Validation
We will determine if individualized hybrid imaging maps (HIMs) based on a pre-operative imaging panel accurately predicts the actual cancer distribution found in the whole mount prostatectomy specimens obtained from the surgery.
Secondary Outcome Measures
Full Information
NCT ID
NCT04009174
First Posted
October 24, 2018
Last Updated
March 16, 2023
Sponsor
Lawson Health Research Institute
Collaborators
Canadian Institutes of Health Research (CIHR)
1. Study Identification
Unique Protocol Identification Number
NCT04009174
Brief Title
Multi-modality Prostate Cancer Image Guided Interventions
Acronym
IGPC-2
Official Title
Multi-modality Prostate Cancer Image Guided Interventions
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 12, 2012 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lawson Health Research Institute
Collaborators
Canadian Institutes of Health Research (CIHR)
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 is a non-randomized, prospective trial of men who are scheduled for radical prostatectomy for treatment of prostate cancer, or repeat biopsy for localized prostate cancer as standard of care and who will undergo a series of pre-operative multi-modality imaging studies. Post intervention, hybrid imaging maps (HIM) will be generated and the predictions of the HIM (3D location, volume and grade of cancer) will be correlated with actual pathology results to gauge the performance of the HIM in both radical prostatectomy and biopsy settings.
Detailed Description
This study was built on our first study (IGPC-1, REB number 15551) which acquired multi-modality imaging in 36 patients undergoing radical prostatectomy. We successfully demonstrated the ability to accurately co-register pre-operative multi-modality images (MRI: T1, T2, Diffusion Weighed (DW), Dynamic Contrast enhanced (DCE); Dynamic Contrast Enhanced CT, 3D Ultrasound with post-operative whole mount pathology specimens. We have developed a platform for the segmentation of prostate cancer on the whole mount pathology specimens and are in the process of analyzing the data to develop a hybrid imaging map (HIM) of prostate cancer distribution (location and grade) based on the correlation of the pre-operative imaging signals and the post-operative pathology (citation provided below). The HIM will need subsequent validation in a separate cohort of radical prostatectomy patients and evaluated as to its ability to be incorporated as a targeting tool for prostate interventions such as prostate biopsy and this is the purpose of this follow-up study.
On the IGPC-2 study, pre-operative imaging panels were successfully obtained in 24 patients accrued to cohort 1. The protocol was then amended to include [18-F]-DCFPyl instead of [18F]-FCH. [18-F]-DCFPyl was a newer PET probe that may possess superior performance because it is directed against prostate specific membrane antigen (PSMA), a protein commonly expressed on prostate cancer cells. Imaging-pathology correlations in the first 6 patients imaged with [18-F]-DCFPyl were compared to the correlations obtained with [18F]-FCH imaging in the first 24 patients.
IGPC-2 Cohort 1 (Radical Prostatectomy) was expanded to provide an additional 20 men imaged with [18-F]-DCFPyl as part of the imaging panel. The goal was to acquire 24 complete imaging datasets with [18-F]-DCFPyl as the PET imaging agent to enable us to draw comparisons with the 24 [18F]-FCH imaging data sets acquired.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate Cancer, PET/CT, PET/MRI, Fluorocholine, PSMA, Sodium (Na) MRI, [18-F]-FCH, [18-F]-DCFPyL, Hybrid imaging, Whole mount histopathology
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
52 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Imaging Panel
Arm Type
Experimental
Arm Description
Patients who provided written informed consent and found to be eligible for study were asked to complete Positron Emission Tomography (PET) + Dynamic CT imaging, PET/MRI (with endorectal coil) and 3D-Transrectal ultrasound prior to standard of care radical prostatectomy.
Intervention Type
Other
Intervention Name(s)
Imaging Panel
Intervention Description
Initial Protocol (REB approval date 08-Sept-2011)
Pre-operative Imaging Panel
[18F]-FCH PET + Dynamic CT
MRI of the pelvis with endorectal coil (T1, T2, DW, DCE, MRS)
3D-Transrectal ultrasound
Optional PET/MRI (added with Protocol Amend 1, REB approval date 22-Aug-2012)
Optional Sodium (23Na) MRI (added with Protocol Amend 2, REB approval date 25-Feb-2013)
Protocol Amendment #3, REB approval date 20-Oct-2015:
Pre-operative Imaging Panel
[18-F]-DCFPyL PET+Dynamic CT
PET/MRI with endorectal coil
3D-Transrectal Ultrasound
Optional Sodium (23Na) MRI
Primary Outcome Measure Information:
Title
Hybrid Imaging Map (HIM) Validation
Description
We will determine if individualized hybrid imaging maps (HIMs) based on a pre-operative imaging panel accurately predicts the actual cancer distribution found in the whole mount prostatectomy specimens obtained from the surgery.
Time Frame
Within two years of study completion.
Other Pre-specified Outcome Measures:
Title
MRI Prostate Sodium Imaging Validation
Description
We will determine if sodium levels in the prostate based on a pre-operative sodium MRI accurately predicts the actual cancer distribution found in the whole mount prostatectomy specimens obtained from the surgery.
Time Frame
Within two years of study completion
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Male with a prostate
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Provision of informed consent for this study
Male, aged 18 years or older
Pathologically confirmed prostate cancer on previous biopsy
Suitable for and consenting to Radical Prostatectomy for treatment, or repeat biopsy as standard of care
Exclusion Criteria:
Prior therapy for prostate cancer (including hormone therapy), with the exception of radiation therapy for Cohort 2 only
Use of 5-alpha reductase inhibitors, i.e. finasteride (Proscar) or dutasteride (Avodart) within 6 months of study start. Patients undergoing a 6-month washout period prior to study start will be eligible.
Inability to comply with the pre-operative imaging panel
Patients scheduled for radical prostatectomy with prostate size exceeding dimensions for whole mount pathology slides
Allergy to contrast agents to be used as part of the imaging panel
Sickle cell disease or other anemias
Insufficient renal function (eGFR < 60 mL/min/1.73 m2)
Residual bladder volume > 150 cc (determined by post-void ultrasound)
Hip prosthesis, vascular grafting that is MRI incompatible or sources of artifact within the pelvis
Contraindication to MRI
pacemaker or other electronic implants
known metal in the orbit
cerebral aneurysm clips
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr. Glenn Bauman, MD
Organizational Affiliation
Lawson Health Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5W9
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Fully anonymized study data such as de-identified images, digital pathology slides, prostate tissue slides and prostate cancer diagnosis information can be available for data analysis.
IPD Sharing Access Criteria
Institutionally approved material sharing agreement.
Citations:
Citation
Ward A, Crukley C, McKenzie C, Montreuil J, Gibson E, Gomez JA, et al. Registration of in vivo prostate magnetic resonance images to digital histopathology images. MICCAI'10 Proceedings of the 2010 international conference on Prostate cancer imaging: computer-aided diagnosis, prognosis, and intervention; Bejing, China. Berlin: Springer-Verlag; 2010.
Results Reference
background
PubMed Identifier
34652551
Citation
Yang DM, Alfano R, Bauman G, Thiessen JD, Chin J, Pautler S, Moussa M, Gomez JA, Rachinsky I, Gaed M, Chung KJ, Ward A, Lee TY. Short-duration dynamic [18F]DCFPyL PET and CT perfusion imaging to localize dominant intraprostatic lesions in prostate cancer: validation against digital histopathology and comparison to [18F]DCFPyL PET/MR at 120 minutes. EJNMMI Res. 2021 Oct 15;11(1):107. doi: 10.1186/s13550-021-00844-0.
Results Reference
derived
PubMed Identifier
33394284
Citation
Yang DM, Li F, Bauman G, Chin J, Pautler S, Moussa M, Rachinsky I, Valliant J, Lee TY. Kinetic analysis of dominant intraprostatic lesion of prostate cancer using quantitative dynamic [18F]DCFPyL-PET: comparison to [18F]fluorocholine-PET. EJNMMI Res. 2021 Jan 4;11(1):2. doi: 10.1186/s13550-020-00735-w.
Results Reference
derived
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Multi-modality Prostate Cancer Image Guided Interventions
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