⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Diagnosing Clinically Significant Prostate Cancer In African American and White Men With Elevated PSA

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Diagnosing Clinically Significant Prostate Cancer In African American and White Men With Elevated PSA

Official Title: Diagnosing Clinically Significant Prostate Cancer in African American and White Men Phase II, Randomized Clinical Trial, Multi-center, MR-Guided vs. 12-core Systematic Random Biopsy, Localized Prostate Cancer

Study ID: NCT03234556

Study Description

Brief Summary: This randomized phase II trial studies how well systematic random biopsy or magnetic resonance imaging (MRI)-ultrasound image (US) fusion biopsy work in diagnosing prostate cancer in patients with elevated prostate specific antigen. Systematic random biopsy and MRI-US fusion biopsy may work better in improving the accuracy of prostate cancer detection.

Detailed Description: PRIMARY OBJECTIVES: I. To compare the detection of clinically significant prostate cancer (CSPCa) in Arm 1 versus Arm 2. II. To compare between African American (AA) and white men the probability of developing CSPCa within three years of initial biopsy at the start of the study. SECONDARY OBJECTIVES: I. To determine complications and patient morbidity associated with either systematic random prostate biopsy (SR-Bx) versus (vs) magnetic resonance imaging-ultrasound image fusion biopsy (MRUS-Bx) + SR-Bx. TERTIARY OBJECTIVES: I. To compare Gleason score between MRUS-Bx and radical prostatectomy (RP) specimen among men who elect RP (\~110 in the randomized controlled trial \[RCT\]). II. To assess within Arm 1 the detection of CSPCa three months after SR-Bx among men initially diagnosed with clinically insignificant prostate cancer (CinsPCa) or no cancer. III. To identify among men invited to participate and those actually enrolled in the RCT: determinants of study participation. IV. To identify among men invited to participate and those actually enrolled in the RCT: determinants of treatment decision (active surveillance \[AS\] vs radiation vs RP) including the diagnostic method. OUTLINE: Patients are randomized into 1 of 2 arms. ARM I: SR-Bx group * Patients undergo SR-Bx * If SR-Bx doesn't reveal clinically significant cancer, then MRI in 3 months, and if lesion is present (PIRADS ≥ 3) schedule for MRUS-Bx. * If there is no lesion, then no biopsy - schedule MRI in 12 months after the initial MRI. ARM II: MRUS-Bx group * Patients undergo MRI. Must be scheduled at least 1 day before MRUS Biopsy. * MRI shows no lesion present (PIRADS 1-2): no MRUS-Bx, schedule for SR-Bx only. * MRI lesion present (PIRADS ≥ 3): schedule for MRUS-Bx, which will be done first and followed immediately after by SR-Bx. FOLLOW UP: After completion of procedure, patients are followed up at 2-4 weeks, 3, 6, 9, and 12 months, and then periodically for up to 5 years.

Keywords

Eligibility

Minimum Age: 40 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States

University of Maryland, Baltimore, Maryland, United States

Henry Ford Hospital Vattikuti Urology Institute, Detroit, Michigan, United States

Memorial Sloan-Kettering Cancer Center, New York, New York, United States

Contact Details

Name: Inderbir Gill

Affiliation: University of Southern California

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: