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Collecting Blood Samples From People With Prostate Cancer

Collects blood from men with prostate cancer to study gene differences linked to disease progression.

Plain-language title generated from the registry record
Registry title: Collection of Blood From Patients With Prostate Cancer

Key facts

Where
Bethesda, United StatesSee the site

Where in United States

  • National Institutes of Health Clinical CenterBethesda, United StatesTaking people

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Trial details

Who runs it
National Cancer Institute (NCI)
Trial code
NCT00923221
Record updated
9 November 2026
Original description
Background:Read full original descriptionShow less

Collection of Blood From Patients With Prostate Cancer

Background:

* It is not fully understood why prostate cancer in some men becomes androgen-independent (no longer responds to anti-androgen medication), but genetics likely plays an important role. * Genes contain the hereditary information that is passed down from parents to children. Although everyone has the same set of genes, individuals can have different forms of the same gene. * Differences in genes may explain, at least in part, why some people develop a more aggressive form of prostate cancer than others.

Objectives:

-To obtain blood samples from patients with prostate cancer to try to identify gene differences associated with progression to the androgen independent state.

Eligibility:

-All participants participating in NCI prostate cancer protocols.

Design:

* Participants with prostate cancer are evaluated in the NCI s Medical Oncology Clinic. * Blood samples are collected at the initial visit or at follow-up visits. * DNA (genetic material) and white blood cells are extracted from these samples to be used for genotyping and establishment of cell lines. * Gene variations are correlated with prostate cancer prognosis and prognostic indicators.

Exclusion: Children are not eligible.

INCLUSION CRITERIA:; Individuals 18 years of age and older are eligible; Individuals with a diagnosis of prostate cancer are eligible.

ClinicalTrials.gov NCT00923221