Actively Recruiting

Age: 2Years +
All Genders
Healthy Volunteers
ID00026884

Collection of Serum and Tissue Samples From Patients With Biopsy-Proved or Suspected Malignant Diseases

Led by National Cancer Institute (NCI) · Updated on 2026-06-08

5950

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Collection of Serum and Tissue Samples From Patients With Biopsy-Proved or Suspected Malignant Disease

Who Can Participate

Age: 2Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals with biopsy-proven malignant disease
  • Individuals suspected of having a malignant disease
  • Individuals who have or are suspected of having an inherited genitourinary malignant disorder
  • Participants must be 2 years of age or older
  • A relative (related by blood) of an individual with a confirmed or suspected diagnosis of a malignant disease or an inherited genitourinary malignant disorder
  • All participants and parents/guardians for children younger than 18 years must sign an informed consent indicating understanding of the investigational nature and risks of the study
Not Eligible

You will not qualify if you...

  • Individuals whose co-morbidities preclude surgical intervention

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

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

Long-term Monitoring

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

Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

D

Deborah A Nielsen, R.N.

W

W. Marston Linehan, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

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