Spinal tap could replace brain surgery for young tumor patients
NCT ID NCT05934630
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a liquid biopsy—testing the fluid around the brain and spinal cord—can find tumor DNA in children and young adults with brain tumors. The goal was to see if this safer, non-surgical test could replace risky tissue biopsies for diagnosis and monitoring. Up to 300 participants provided extra fluid samples during routine care, and their results were compared with tumor tissue samples.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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57 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Apr 2026
- Lead sponsor
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A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients will enroll from and be seen at Pediatric Brain Tumor Consortium sites and will meet the eligibility criteria in order to participate.
- Ages
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Up to 40 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: All patients must have a known or suspected diagnosis (based on pathology or imaging) of a primary brain tumor. All children and adolescent/young adult (AYA) patients =\< 21 years of age are eligible. AYA patients \< 40 are eligible with a primary brain tumor entity more common in children than adults. This includes: * medulloblastoma * non-medulloblastoma embryonal brain tumors * atypical teratoid rhabdoid tumors (ATRT) * ependymoma * CNS germ cell tumors * Diffuse midline glioma, H3K27M-altered * Diffuse hemispheric glioma, H3 G34-mutant * pineoblastoma * diffuse leptomeningeal glioneuronal tumor * diffuse brainstem glioma * pilocytic astrocytoma * choroid plexus carcinoma ELIGIBLE PATIENTS WILL BE STRATIFIED BY DIAGNOSIS AS FOLLOWS: * Stratum 1: Medulloblastoma * Stratum 2: High-grade glioma (IDH-wildtype) and DIPG o DIPG patients must meet clinical and imaging requirements for DIPG diagnosis. Patients with newly diagnosed diffuse intrinsic pontine gliomas (DIPGs), defined as tumors with a pontine epicenter and diffuse involvement of 2/5 or more of the pons, are eligible without histologic confirmation. Patients with brainstem tumors that do not meet these criteria or not considered to be typical intrinsic pontine gliomas will only be eligible for Stratum B if the tumors have been biopsied and are proven to be an anaplastic astrocytoma, glioblastoma multiforme, gliosarcoma, anaplastic mixed glioma or fibrillary astrocytoma. * Stratum 3: Low-grade glioma (IDH-wildtype) with multifocal/disseminated and/or leptomeningeal disease * Stratum 4: Diffuse Leptomeningeal Glioneuronal Tumor * Stratum 5: Pineoblastoma * Stratum 6: All other eligible tumor types * DISEASE STATUS: Participants will be eligible at any stage of disease. * AGE: All children and adolescent/young adult (AYA) patients =\< 21 years of age are eligible. AYA patients \< 40 are eligible with a primary brain tumor entity more common in children than adults * CEREBROSPINAL FLUID (CSF) COLLECTION: Patients must have a clinical indication for at least one CSF (lumbar, cisternal or ventricular) collection, or clinical circumstance where CSF sampling is feasible with no or minimal risk (e.g., endoscopic third ventriculostomy, external ventricular drain). * INFORMED CONSENT: The patient or parent/guardian can understand the consent and is willing to sign a written informed consent document according to institutional guidelines. Exclusion Criteria: * DIAGNOSIS: Given the extremely low rate of CSF cfDNA positivity in patients with localized, non-disseminated low-grade glioma, those patients will be excluded from participation.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611, United States
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Children's Hospital of Los Angeles
Los Angeles, California, 90026, United States
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Children's Hospital of Pittsburgh of UPMC
Pittsburgh, Pennsylvania, 15224, United States
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Children's National Medical Center
Washington D.C., District of Columbia, 20010, United States
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Cincinnati Childrens Hospital Medical Center
Cincinnati, Ohio, 45229, United States
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Hospital for Sick Children
Toronto, Ontario, M5G1X8, Canada
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Lucille Packard Children's Hospital Stanford University
Palo Alto, California, 94304, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Nationwide Childrens Hospital
Columbus, Ohio, 43205, United States
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Texas Children's Hospital
Houston, Texas, 77030, United States
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Other studies related to the condition(s) this trial covers.
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