This phase II trial studies how well multiparametric magnetic resonance imaging (MRI) works in evaluating cancer stage and helping treatment planning in patients with prostate cancer. Multiparametric MRI may be useful for evaluating the type of cancer in finding aggressive disease.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT03697148.
PRIMARY OBJECTIVES:
I. To estimate the diagnostic performance of overall prostate imaging reporting and data system (PI-RADS) score based on local site imaging review of multiparametric (mp) MRI (T2 weighted [2W], diffusion weighted imaging [DWI] and dynamic contrast-enhanced [DCE]) to detect clinically significant prostate cancer.
II. To develop and evaluate a risk prediction model by incorporating overall PI-RADS, PSA, Gleason score and clinical stage to predict the presence of clinically significant prostate cancer.
SECONDARY OBJECTIVES:
I. To evaluate the diagnostic performance of the individual PI-RADS score of each MRI parameter (T2W, DWI and DCE), as determined by local imaging review.
II. Estimate the diagnostic performance of PI-RADS version (v)2.1 for detecting clinically significant prostate cancer among Black or African Americans participants.
EXPLORATORY OBJECTIVE:
I. All clinical data including magnetic resonance (MR) images will be banked for future exploratory research aims.
EXPLORATORY TOBACCO USE OBJECTIVES:
I. To determine the effects of tobacco, operationalized as combustible tobacco (1a), other forms of tobacco (1b), and environmental tobacco exposure (ETS) (1c) on provider-reported cancer-treatment toxicity (adverse events [both clinical and hematologic]) and dose modifications.
II. To determine the effects of tobacco on patient-reported physical symptoms and psychological symptoms.
III. To examine quitting behaviors and behavioral counseling/ support and cessation medication utilization.
IV. To explore the effect of tobacco use and exposure on treatment duration, relative dose intensity, and therapeutic benefit.
OUTLINE:
Patients undergo mpMRI within 3 months prior to scheduled surgery.
After completion of study, patients are followed up until radical prostatectomy pathology is reported and finalized.
Lead OrganizationECOG-ACRIN Cancer Research Group
Principal InvestigatorClare M.C. Tempany-Afdhal