CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2015-2019.
Quinn T Ostrom, Mackenzie Price, Corey Neff...
https://pubmed.ncbi.nlm.nih.gov/36196752Actively Recruiting
Led by National Cancer Institute (NCI) · Updated on 2026-05-22
80
Participants Needed
1
Research Sites
N/A
Total Duration
Primary central nervous system (CNS) tumors, which include recurrent gliomas and other rare brain tumors, are challenging to treat and often have poor outcomes. This research evaluates a new AI-driven technology called SmartMatch, developed to analyze how tumor tissue samples respond to various FDA-approved drugs. The goal is to see if SmartMatch can provide drug response results within 21 days after tumor tissue is collected to help doctors explore better treatment options for patients with advanced CNS tumors. During the study, participants who are scheduled for tumor biopsy or surgery at NIH will have small tumor samples collected as part of their planned procedure. These fresh samples will be analyzed using the SmartMatch platform to generate drug response data. Blood samples will also be collected for additional molecular profiling. The study does not require any extra procedures beyond what is planned for clinical care. Participants will be followed remotely every six months for up to three years to monitor their health and any disease progression. The research team will review how quickly and effectively the SmartMatch platform completes the drug screen analysis and will gather molecular information about the tumors over time. The study aims to improve understanding of CNS tumors and support the development of more precise treatments in the future.
CONDITIONS
Observational Study of Responses to Treatments in Advanced Central Nervous System (CNS) Tumors
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 visit (in-person) for eligibility confirmation and informed consent
Duration - Day of planned biopsy or resection
Participants undergo a planned brain tumor biopsy or resection at NIH to collect fresh tumor samples for SmartMatch drug screen analysis and molecular profiling.
1 visit (in-person) for tumor biopsy or resection
Duration - Up to 3 years
Participants are followed remotely every 6 (+/-3) months for up to 3 years to monitor outcomes after tumor sample collection.
Remote follow-up every 6 months (+/- 3 months)
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
C
Christine T McGowan
J
Jing Wu, M.D.
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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