NCT05934630Terminated
Testing Cerebrospinal Fluid for Cell-free Tumor DNA in Children, Adolescents, and Young Adults With Brain Tumors
CSF Cell-free Tumor DNA (CSF cfDNA) Liquid Biopsies for Pediatric, Adolescent, and Young Adult Patients With Primary Brain Tumors
Source: ClinicalTrials.gov · Last updated 23 Apr 2026
Reason given: The NCI will not extend the PBTC grant beyond March 31, 2026.
Brief summary (registry, in English)
Recent advances in technology have allowed for the detection of cell-free DNA (cfDNA). cfDNA is tumor DNA that can be found in the fluid that surrounds the brain and spinal cord (called cerebrospinal fluid or CSF) and in the blood of patients with brain tumors. The detection of cfDNA in blood and CSF is known as a "liquid biopsy" and is non-invasive, meaning it does not require a surgery or biopsy of tumor tissue. Multiple studies in other cancer types have shown that cfDNA can be used for diagnosis, to monitor disease response to treatment, and to understand the genetic changes that occur in brain tumors over time. Study doctors hope that by studying these tests in pediatric brain tumor patients, they will be able to use liquid biopsy in place of tests that have more risks for patients, like surgery. There is no treatment provided on this study. Patients who have CSF samples taken as part of regular care will be asked to provide extra samples for this study. The study doctor will collect a minimum of one extra tube of CSF (about 1 teaspoon or 5 mL) for this study. If the patients doctor thinks it is safe, up to 2 tubes of CSF (about 4 teaspoons or up to 20 mL) may be collected. CSF will be collected through the indwelling catheter device or through a needle inserted into the lower part of the patient's spine (known as a spinal tap or lumbar puncture). A required blood sample (about ½ a teaspoon or 2 3 mL) will be collected once at the start of the study. This sample will be used to help determine changes found in the CSF. Blood will be collected from the patient's central line or arm as a part of regular care. An optional tumor tissue if obtained within 8 weeks of CSF collection will be collected if available. Similarities between changes in the DNA of the tissue that has caused the tumor to form and grow with the cfDNA from CSF will be compared. This will help understand if CSF can be used instead of tumor tissue for diagnosis. Up to 300 people will take part in this study. This study will use genetic tests that may identify changes in the genes in the CSF. The report of the somatic mutations (the mutations that are found in the tumor only) will become part of the medical record. The results of the cfDNA sequencing will be shared with the patient. The study doctor will discuss what the results mean for the patient and patient's diagnosis and treatment. Looking for inheritable mutations in normal cells (blood) is not the purpose of this study. Genetic tests of normal blood can reveal information about the patient and also about the their relatives. The doctor will discuss what the tests results may mean for the patient and the their family. Patient may be monitored on this study for up to 5 years.
- Status (registry)
- Terminated
- Study type
- Observational
- Enrollment
- 57 (actual)
- First submitted
- 28 Jun 2023
- Start date
- 12 Jul 2023
- Primary completion date
- 17 Apr 2026
- Lead sponsor
- Pediatric Brain Tumor Consortium
- Diseases
- Childhood cancers, Glioblastoma
- NCT number
- NCT05934630
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- 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.
Who the study is looking for
- 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.
Age in the registry: - to 40 years · Sex: All · Does not accept healthy volunteers
Sites (10)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hospital for Sick Children | Toronto | Canada | Unknown status |
| Ann & Robert H. Lurie Children's Hospital of Chicago | Chicago | United States | Unknown status |
| Cincinnati Childrens Hospital Medical Center | Cincinnati | United States | Unknown status |
| Nationwide Childrens Hospital | Columbus | United States | Unknown status |
| Texas Children's Hospital | Houston | United States | Unknown status |
| Children's Hospital of Los Angeles | Los Angeles | United States | Unknown status |
| Memorial Sloan-Kettering Cancer Center | New York | United States | Unknown status |
| Lucille Packard Children's Hospital, Stanford University | Palo Alto | United States | Unknown status |
| Children's Hospital of Pittsburgh of UPMC | Pittsburgh | United States | Unknown status |
| Children's National Medical Center | Washington D.C. | United States | Unknown status |
Are you the coordinator? Confirm the details
In 2 countries, 10 sites
United States 9, Canada 1
The registry text, word for word
This page is information, not medical advice. Discuss any trial with your doctor.