Prostate Cancer Clinical Trial
Official title:
MR Imaging to Stratify Prostate Cancer Progression Risk in Patients on Active Surveillance
RATIONALE: Sometimes prostate cancer may not need treatment until it progresses. In this
case, active surveillance may be sufficient. Diagnostic procedures, such as magnetic
resonance imaging, may be a less invasive method of finding prostate cancer that has
progressed.
PURPOSE: This clinical trial is studying how well magnetic resonance imaging works in
detecting cancer progression in patients with early-stage prostate cancer who are undergoing
active surveillance.
OBJECTIVES:
Primary
- To determine if MRI parameters (initial volume, number and location of image
abnormalities, and MR spectroscopy) can improve the ability to stratify cancer
progression risk in patients undergoing active surveillance for early-stage prostate
cancer.
Secondary
- Determine if changes in non-invasive MRI, validated by MRI-guided biopsies, can
accurately detect progression of prostate cancer.
OUTLINE: Patients undergo prostate MRI scans and MRI-guided biopsies of suspicious lesions
at baseline. Patients undergo conventional anatomic imaging followed by research biological
imaging tests (e.g., magnetic resonance spectroscopic imaging and/or dynamic
contrast-enhanced MRI). MRI are repeated at 6 months, 1 year, and then annually until
initiation of definitive therapy or for a total of 5 years.
Tissue biopsy with MRI guidance is done at baseline and annually or as clinically indicated
based on change in rectal exam, PSA, or maybe done based on change in MR imaging (i.e., new
MR lesion or significant change [> 25% increase] in the size of a MR lesion).
Blood samples are collected at baseline and periodically during study for PSA tests.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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