Prostate Cancer Clinical Trial

EDRN Prostate MRI Biomarker Study

Summary

The commercialization of MRI fusion biopsies has resulted in a dramatic increase in the use of MRI imaging for prostate cancer. How best to use MRI in the initial prostate biopsy setting given the availability of validated prostate cancer early detection markers is uncertain.This study will allow investigators to determine if prostate MRI is superior to validated panel of laboratory biomarkers (e.g. PCA3, PSA and TMPRSS2:ERG) in the initial biopsy setting.

View Full Description

Full Description

The primary aim of this study is to see if the addition of prostate MRI to a panel consisting of PSA, PCA3, TMPRSS2:ERG will significantly improve specificity for high-grade prostate cancer by 10%. The subsequent exploratory aims will 1) create an optimal panel of urine, blood and tissue biomarkers that will select those cases most likely to benefit from a MRI targeted biopsy, 2) directly compare PSA and urinary biomarkers with MRI to determine which ones are value added in the setting of initial biopsy, 3) evaluate changes in these biomarkers and MRI to determine if longitudinal changes predict subsequent high-grade prostate cancer, and 4) optimize MRI imaging to improve test performance. Importantly, this study will create a unique, prospective, cohort that will become the foundational reference set for of a range of future biomarker studies.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Men with suspected but undiagnosed prostate cancer
To be scheduled/scheduled for biopsy as routine clinical care

Exclusion Criteria:

Inability to obtain blood and urine per SOP or conduct an attentive DRE
Unable to undergo/tolerate a prostate MRI or failure to conduct the MRI
Prior diagnosis of prostate cancer
Prior prostate MRI unless being used as Index MRI (in this case index MRI can be one year prior to consent date)
Participating in clinical trial for prostate disease
Prior prostate surgery such as TURP, TUNA, TUMT, HOLEP, REZUM, UROlift
Prior PCA3, TMPRSS2:erg or MIPS panel performed for clinical purpose

Study is for people with:

Prostate Cancer

Estimated Enrollment:

1500

Study ID:

NCT03784924

Recruitment Status:

Recruiting

Sponsor:

University of Michigan

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There is 1 Location for this study

See Locations Near You

University of Michigan
Ann Arbor Michigan, 48109, United States More Info
John T Wei, MD
Contact
734-615-3040
[email protected]
Rabia Martin
Contact
7347637508
[email protected]

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Estimated Enrollment:

1500

Study ID:

NCT03784924

Recruitment Status:

Recruiting

Sponsor:


University of Michigan

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.