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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age2+
SponsorNational Cancer Institute (NCI)

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

5,950 Participants
are grouped into 2 trial groups
Group A: Family Members
Group B: Participants

Trial outcomes

Primary outcomes

1

Investigate quality of life in men who have prostate cancer.

Prostate cancer participants that have improvement in quality of life

Time frame
on-going
2

Investigate molecular genetic basis of urologic malignancies

Investigate molecular genetic basis of urologic malignancies

Time frame
on-going
3

Investigate cellular/biochemical response to existing and novel therapeutic agents.

Collection of blood, urine, saliva, and/or benign and malignant tissue

Time frame
on-going
4

Examine protein expression and bioimmunoassays investigating potential genetic markers.

Detection and expression analysis of gene(s)

Time frame
on-going

Secondary outcomes

Other outcomes

Sponsors and contacts

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