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/37404084/Actively Recruiting
Led by National Cancer Institute (NCI) · Updated on 2026-07-02
5950
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying the genetic causes and molecular characteristics of urologic cancers including kidney, prostate, bladder, testis, and penile cancers. These cancers make up a significant portion of cancer diagnoses and deaths in the United States. The goal is to better understand gene pathways involved in these malignancies to aid in developing targeted treatments. This observational study collects blood, urine, and tissue samples from individuals with confirmed or suspected malignant disease or inherited urologic cancer risks. Participants include patients with biopsy-proven or suspected malignancies and their blood relatives who may have inherited cancer risks. Samples of blood, urine, and both normal and malignant tissue are collected during clinical visits and surgeries. These specimens are stored in a tissue bank and used for genetic sequencing, protein expression analysis, and research on cancer gene mutations and biochemical pathways. The study also investigates quality of life in men with prostate cancer and responses to existing and novel cancer therapies. During the study, participants undergo eligibility screening and may provide biological samples at initial and periodic visits. Tissue samples are collected during clinically indicated surgeries. Researchers analyze these samples using molecular and biochemical methods to identify genetic differences and markers. Participants may be contacted if significant health-related findings arise. The study involves ongoing assessments of genetic and molecular data and quality of life, continuing over time without a fixed end date.
CONDITIONS
Collection of Serum and Tissue Samples From Patients With Biopsy-Proved or Suspected Malignant Disease
D
Deborah A Nielsen, R.N.
W
W. Marston Linehan, M.D.
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National Cancer Institute (NCI)
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Ongoing
Participants provide blood and urine samples during clinic visits. Tissue samples are collected during clinically indicated surgeries and stored for research. Collected samples are analyzed to study genetic and molecular features of urologic cancers.
Periodic visits as clinically indicated
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/National Cancer Institute (NCI)
Lead Sponsor