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UCSF Biobank for Studying Hereditary Cancers and Tumor-Associated Mutations
This is a non-therapeutic clinical research biorepository protocol designed to obtain, store, and clinically annotate biospecimens from participants with hereditary cancers. Those biospecimens will be used to generate participant-derived tumor models that will serve as a resource to better understand hereditary cancers and develop new efficient therapies.
Primary Objective: 1. To generate a repository of participant-derived tumor models\* and specimens\*\* - annotated with demographic, clinical, and pathologic data - from adults with solid tumor malignancies with germline or somatic tumor-associated mutations and/or a personal or family history of cancer. * Participant-derived models may include (but are not limited to) xenografts (PDX), organoids (PDO), and cell lines (PDCLs). * Specimens may include tissue, ascites and pleural fluid, and blood. Exploratory Objectives 1. To correlate in vivo drug sensitivity of participant-derived models with patient clinical response. 2. To conduct blood-based assessment of tumor-associated biomarkers (DNA/RNA/protein, etc.). 3. To describe tumor and blood-based biomarkers that are predictive of clinical response. 4. To correlate changes in tumor and blood-based biomarker expression with clinical outcomes over time. 5. To perform genomic and transcriptomic profiling of banked specimens and correlate findings with clinical outcomes, prognostic markers, and biomarkers. 6. Unspecified cancer-centric research in the Munster Lab and other future unspecified research. OUTLINE: Participants will have biospecimens collected at non-study, routine procedures or visits to be stored at UCSF. Specimens will be processed and banked as per standard operating procedure. Participants will be followed through medical record chart review for a period of 10 years after signing informed consent, and be contacted every 3 months (± 2 months) for the first year and every 6 months (± 3 months) thereafter to allow updates to health status.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of California, San Francisco
San Francisco, California, United States
Start Date
January 31, 2026
Primary Completion Date
December 31, 2035
Completion Date
December 31, 2035
Last Updated
November 10, 2025
50,000
ESTIMATED participants
Blood Sample
PROCEDURE
Tissue Sample
PROCEDURE
Excess fluid Sample
PROCEDURE
Medical Chart Review
OTHER
Lead Sponsor
University of California, San Francisco
NCT06898450
NCT05720117
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06658951