Molecular Characterization of Viral-associated Tumors, Tumors Occurring in the Setting of HIV or Other Immune Disorders and Castleman Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNational Cancer Institute (NCI)

About this trial

Background:

A person s genome is the collection of all their genes. A gene instructs individual cells to make proteins. Proteins are involved in all of our body s chemical processes. Genome sequencing allows researchers to find variations in genes. Some of these are normal and are not known to cause disease. Some variants are known to cause or affect diseases like cancer. Researchers want to study genetic variants in people with cancer who also have an immunologic disease like HIV.

Objective:

To study the biology of cancer in order to improve ways to prevent, detect, and treat it.

Eligibility:

Adults at least 18 years old with certain cancers and/or immunodeficiencies

Design:

Participants will be screened with medical history, physical exam, and lab tests.

Participants will give samples of one or more tissue type.

They may give blood or urine samples.

Researchers may get samples of tissue when participants have surgery or when the participants are on other protocols in the NCI.

Participants may have a procedure to have tissue samples removed.

Researchers may collect data from participant medical records.

Researchers will compare the genes in a participant s cancer tissue to their normal tissue. They may use the tissue cells to grow new cells in a lab.

Participants may be contacted about the results.

The samples will be stored for future research. No personal data will be kept with them.

...

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

HIV or other acquired immunodeficiency and cancer

Viral-associated cancer or cancer hypothesized to be caused by a virus

HIV-negative participants with cancer that commonly occurs in people with HIV

A malignancy hypothesized to be caused by an endogenous retrovirus

Disqualifiers

Inability to provide informed consent.

Pregnancy: Pregnant women will not be allowed to participate in this study because there is not a potential benefit.

Trial population

The study population will be participants referred by HIV providers and those who provide primary care to the African immigrant community.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

280 Participants
are grouped into 1 trial group
Group A: group 1

Trial outcomes

Primary outcomes

1

Tissue collection

Molecular data from viral associated malignancies, malignancies occurring in the setting of HIV or other immunodeficiencies, and Castleman disease

Time frame
Time of collection

Secondary outcomes

Other outcomes

Sponsors and contacts

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