Correlation of Imaging Findings With Clinical Findings and Patient Outcomes in Prostate Cancer

Prostate Cancer Clinical Trial

Official title:

Assessment of Advanced Imaging Techniques in the Evaluation and Management of Prostate Cancer

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT03122470
• Other study ID #: CASE10815
• Status: Withdrawn
• Phase: N/A
• Start date: August 1, 2017
• Est. completion date: June 20, 2023

Study information

• Verified date: March 2023
• Source: Case Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

MRI is being increasingly relied upon for detection, staging and management of prostate cancer. In this study patients with risk of prostate cancer will be recommended to have a pelvic MRI prior to the standard biopsy of the prostate and standard treatment of any detected prostate cancer. The results of the MRI will be compared to standard diagnosis techniques to see if cancer can be more accurately detected.

Description:

The study team hypothesizes that strategic use of advanced MRI methods will provide a more accurate and less invasive approach for diagnosis and management of prostate cancer. The primary objectives are: 1. To develop advanced MRI methods and optimal MRI protocols for detection, staging, and follow-up of prostate cancer. 2. To evaluate the diagnostic performance of MRI-guided biopsy methods and correlate MRI findings with the pathological grade of cancer. 3. To correlate prostate MRI findings and biopsy results with patient progress and outcomes. 4. To evaluate the diagnostic accuracy of MRI in disease re-classification in patients on active surveillance. Secondary Objectives: 1. To apply computer-aided advanced image analytic techniques (Computer-assisted diagnostics- CAD) to extract MRI features of patient clinical scans that correlate with diagnosis and grade of prostate cancer. 2. To study MRI features of lesions that mimic prostate cancer on imaging eg - chronic prostatitis, post treatment changes. 3. To evaluate the impact of MRI in decision making and choice of treatment by physicians and patients.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: June 20, 2023
• Est. primary completion date: May 20, 2019
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 40 Years to 90 Years

Eligibility

Inclusion Criteria:

• Patients with a suspicion (elevated PSA and/or abnormal digital rectal exam)/ diagnosis of prostate cancer Inclusion criteria for sub-group follow-up scans: 1a. Patients who have undergone standard TRUS biopsy or TRUS with targeted biopsy (i.e cognitive TRUS, MR-TRUS fusion or TRUS + in-gantry biopsy)

Exclusion Criteria:

• Patients with ferromagnetic or otherwise non-MRI compatible aneurysm clips.
• The presence of an implanted pacemaker or implanted defibrillator device.
• Patients with contraindications for MRI due to embedded foreign metallic objects. Bullets, shrapnel, metalwork fragments, or other metallic material adds unnecessary risk to the patient.
• Implanted medical device not described above that is not MRI-compatible;
• Known history of severe claustrophobia;
• For patients with known history of allergic reaction to magnetic resonance (MR) contrast material or abnormal kidney function (glomerular filtration rate (GFR) < 30 mL/min), a contrast enhanced exam will not be performed; however, a non-contrast exam may be performed;
• Minors will be excluded.
• Prisoners and members of other vulnerable populations will be excluded from this study as these populations will not provide any additional unique information to or uniquely benefit from the study.

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Device:
• MRI guided biopsy
The MRI guided biopsy will preferentially be performed using a 3 tesla (3T) Siemens Verio, or 3T Siemens Skyra machine. The multiparametric MRI exam will consist of T1-, T2- and diffusion weighted imaging with or without post-contrast perfusion studies. magnetic resonance fingerprinting (MRF) will be performed before contrast injection. The MRI will be interpreted by two specified radiologists from the research team.

Procedure:
• TRUS biopsy
The TRUS biopsy will be performed per current standard of care. Biopsy cores will be sent to pathology in separately labeled specimen cups. The final pathological results will be compared with pre-biopsy MRI findings.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Case Comprehensive Cancer Center

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of patients with the most likely diagnosis based on the five-point scale - PIRADS	Prostate imaging reporting and data system (PIRADS) scale: 1. Benign; 2. Probably benign; 3. Indeterminate; 4. Probably malignant; 5. Malignant	Up to two weeks after MRI
Primary	Number of patients with true diagnosis based on biopsy pathology	1. Benign; 2. Probably benign; 3. Indeterminate; 4. Probably malignant; 5. Malignant	Up to two weeks after MRI
Secondary	biopsy and MRI based diagnosis match in at least 8/10 patients	The score based on the true diagnosis and most likely diagnosis as agreed on by classifiers is the same in at least 80% of patients	Up to two weeks after MRI
Secondary	Ratio of positive diagnosis as detected by pelvic MRI guided biopsy compared to standard TRUS biopsy	The diagnostic performance of MRI guided biopsy techniques will be compared with standard TRUS biopsy using a single sample of patients undergoing both biopsy techniques. It has been reported that MRI consistently detects a larger number of clinically significant prostate cancers (sensitivity - 0.91 for MRI-guided biopsy vs 0.76 for TRUS biopsy), while avoiding the detection of cancers that are clinically insignificant, as compared to TRUS biopsy.	Up to two weeks after MRI