Comparison of MRI-Based Staging and Pathologic Staging for Predicting Biochemical Recurrence of Prostate Cancer After Radical Prostatectomy.
Katie M Merriman, Stephanie A Harmon, Mason J Belue...
https://pubmed.ncbi.nlm.nih.gov/37404084Actively Recruiting
Led by National Cancer Institute (NCI) · Updated on 2026-06-08
5950
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying genetic factors and molecular pathways involved in various genitourinary cancers, including kidney, prostate, bladder, testis, and penile cancers. These cancers represent a significant portion of cancer diagnoses and deaths in the United States. The study aims to understand the differences between normal and cancerous tissues, investigate gene and protein markers, and examine responses to current and new treatments. The research also includes quality of life studies in men with prostate cancer and explores inherited conditions linked to increased cancer risk. Participants include individuals with biopsy-proven or suspected malignant genitourinary diseases, those with known or suspected inherited cancer disorders, and family members related by blood to affected individuals. Blood and urine samples may be collected, and tissue samples—both benign and malignant—may be obtained during clinically necessary surgeries. The study involves genetic sequencing and molecular analysis of collected specimens, with ongoing investigations into gene mutations and biochemical pathways. During participation, patients will be seen at the Urologic Oncology Branch, where samples will be collected and stored for research. Participants may be contacted if findings relevant to their health arise, with the opportunity for further evaluation. The study involves ongoing assessments of quality of life and molecular genetic outcomes. Participation includes signing informed consent, and the study accommodates both adult and pediatric patients, tracking molecular and clinical data over time.
CONDITIONS
Collection of Serum and Tissue Samples From Patients With Biopsy-Proved or Suspected Malignant Disease
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You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Varies based on clinical procedures
Participants provide blood, urine, and tissue samples during clinically indicated surgical procedures or routine clinical care for research purposes.
Visits occur as needed depending on clinical procedures
Duration - Ongoing as needed
Participants may be contacted for follow-up if research results affecting their health are found, and they may be re-evaluated or re-tested under approved protocols.
Follow-up visits as needed
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
D
Deborah A Nielsen, R.N.
W
W. Marston Linehan, M.D.
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Katie M Merriman, Stephanie A Harmon, Mason J Belue...
https://pubmed.ncbi.nlm.nih.gov/37404084