About this trial
Selected individuals suspected of having or with prior biopsy proof of malignant disease will be seen in the Urologic Oncology Branch, NCI. Blood samples may be collected at the time of the initial visit and at periodic intervals during the course of the disease. These samples will be stored in the tissue bank of the Urologic Oncology Branch. Aliquots of malignant and normal tissue will be collected at the time of surgery and stored in the tissue bank, Urologic Oncology Branch, NCI. These materials will be used in the research efforts of the Urologic Oncology Branch, NCI.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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
Disqualifiers
None
Trial population
1\. Individuals with biopsy-proven malignant disease 2. Individuals suspected of having malignant disease 3. Individuals with known or suspected urologic malignant disorders who have clinically indicated urologic or non-urologic surgical lesion 4. Family members of individuals suspected of having an inherited genitourinary malignancy 5. Family members of individuals with a DNA variant
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Investigate quality of life in men who have prostate cancer.
Prostate cancer participants that have improvement in quality of life
Investigate molecular genetic basis of urologic malignancies
Investigate molecular genetic basis of urologic malignancies
Investigate cellular/biochemical response to existing and novel therapeutic agents.
Collection of blood, urine, saliva, and/or benign and malignant tissue
Examine protein expression and bioimmunoassays investigating potential genetic markers.
Detection and expression analysis of gene(s)
Sponsors and contacts
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