Collection of Human Samples to Study Hairy Cell and Other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment

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

About this trial

Background:

\- Researchers who are studying hairy cell leukemia, and how the disease compares with other disorders, are interested in obtaining additional samples from leukemia patients and healthy volunteers. The investigators are particularly interested in samples from individuals who have diseases that can be treated with a new type of drug called immunotoxin, in which an antibody carrying a toxin binds to a cancer cell and allows the toxin to kill the cell.

Objectives:

\- To collect a variety of clinical samples, including blood, urine, lymph samples, and other tissues, in order to study the samples and develop new treatments for leukemia.

Eligibility:

\- Individuals 18 years of age and older who have been diagnosed with leukemia or other kinds of blood and lymphatic system cancers, or who are healthy volunteers.

Design:

* Individuals who have leukemia will be asked to provide blood, bone marrow, urine, and tumor tissue samples as requested by the researchers. Healthy volunteers will provide only blood and urine samples. * No treatment will be given as part of this protocol.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

18 years of age and older

Desire of the individual to submit data and samples for research

Ability to understand and the willingness to sign a written informed consent document.

Disqualifiers

None

Trial population

Primary clinical population; normal donors

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,263 Participants
are grouped into 2 trial groups
Group A: 1
Group B: 2

Trial outcomes

Primary outcomes

1

Tissue Acquisition

Collection of a variety of clinical samples, including blood, urine, lymphapheresis samples, and other tissues and associated data

Time frame
4 weeks

Secondary outcomes

1

HCL follow-up

Assess long-term treatment complications and disease outcomes in participants with HCL/HCLv

Time frame
about every 2 years

Other outcomes

Sponsors and contacts

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