Intratumor heterogeneity and branched evolution revealed by multiregion sequencing.
Marco Gerlinger, Andrew J Rowan, Stuart Horswell...
https://pubmed.ncbi.nlm.nih.gov/22397650Actively Recruiting
Led by National Cancer Institute (NCI) · Updated on 2026-05-29
1800
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying solid tumors in people undergoing surgery or biopsy to collect tissue samples for cancer research. This observational study aims to identify new molecular and biological targets that could help develop future cancer treatments. Participants include adults and children over 2 years old with suspected or confirmed solid tumors, as well as some without tumors undergoing related procedures. Participants will have blood samples taken before their medical procedure. Some may also undergo leukapheresis, a process to collect white blood cells. During surgery or biopsy, samples of tumor tissue and nearby normal tissue will be collected for research. The removed tumor or growth is sent to a lab for analysis. Follow-up visits occur about six weeks after the procedure, and some participants may have additional follow-ups. Throughout the study, researchers will collect biological samples and gather detailed medical and surgical data to help improve cancer treatment research. Participants will have routine checkups after their procedures, and their health will be monitored as part of the study. The main goal is to use these samples and data to find new cancer treatment targets, with participant involvement lasting as long as needed for sample collection and follow-up.
CONDITIONS
Obtaining Solid Tumor Tissue From People Having Biopsy or Surgery for Certain Types of Cancer
You may qualify if you...
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - Day of intervention
Participants undergo diagnostic, preventative, or therapeutic interventions including biopsy or surgery to collect tissue and biologic samples.
1 visit (in-person) during the planned procedure
Duration - Up to 10 years
Participants are followed to collect detailed history, treatment data, and surgical safety outcomes to help identify novel therapeutic targets.
Follow-up visits as part of routine care
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
C
Cathleen E Hannah, C.R.N.P.
J
Jonathan M Hernandez, M.D.
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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