This study will collect blood from patients with cancer to study the level of cells which
decrease the immune response (suppressor cells) before and after chemotherapy. Patients
18 years of age and older with cancer may participate. This study does not involve
treatment.
Participants will have about 50 ml (3 tablespoonfuls) of blood drawn. Depending on their
condition, patients may be invited to enroll in a clinical research study involving
chemotherapy, radiotherapy, or surgery. Additional 40-ml blood samples may be drawn
during the course of treatment.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT00034216.
Locations matching your search criteria
United States
Maryland
Bethesda
National Institutes of Health Clinical CenterStatus: Active
Contact: National Cancer Institute Referral Office
Phone: 888-624-1937
Background:
- Correlative studies performed on biospecimens of human subjects can be used to
investigate the biology of solid tumors, inform the development of new strategies
for treating those cancers, and evaluate these new therapeutic approaches. Specific
areas of interest include, but are not limited to:
- the underlying mechanisms of tumor-specific immune response and suppression in
cancer patients
- genetic and molecular profiling of tumors through circulating tumor cell (cTC),
circulating DNA, and tissue analysis
- investigation of potential early diagnostic and prognostic indicators for solid
tumors such as cTCs and miRNA expression of serum exosomes
- identification of mechanisms of drug-related adverse events and correlation with
clinical parameters
- the role of commensal gut microbiota in both the innate and adaptive responses to
tumors as well as with the use of anticancer agents
Objectives:
- Analyze biospecimens such as tissue, urine, saliva, stool and blood components,
which include serum, leukocytes, peripheral blood mononuclear cells (PBMC), and
circulating tumor cells (cTC), of human subjects.
- Correlate analysis results with clinical parameters such as demographics,
toxicities, and treatment outcomes.
- Undertake genetic analysis of both prokaryotic and eukaryotic samples for advanced
mutational analysis.
Eligibility:
- Patients and healthy volunteers whose biospecimens are of interest to NIH
investigators.
- 18 years of age or older.
Design:
- Cases will be evaluated by NCI or Interventional Radiology, NIH Clinical Center
personnel. Blood, tissue, urine, saliva or other samples may be collected at the initial
visit and at follow-up visits.
Trial PhaseNo phase specified
Trial TypeNot provided by clinicaltrials.gov
Lead OrganizationNational Cancer Institute
Principal InvestigatorJennifer Laura Marte