Cerebrospinal Fluid Biomarkers for Brain Tumors

Description

This study examines cerebrospinal biomarkers in patients with brain tumors. A biomarker is a measurable indicator of the severity or presence of your disease state. Collecting and storing samples of cerebrospinal fluid from patients with brain tumors to study in the laboratory may help doctors develop new strategies to better diagnose, monitor, and treat brain tumors.

Conditions

Central Nervous System Neoplasm

Study Overview

Study Details

Study overview

This study examines cerebrospinal biomarkers in patients with brain tumors. A biomarker is a measurable indicator of the severity or presence of your disease state. Collecting and storing samples of cerebrospinal fluid from patients with brain tumors to study in the laboratory may help doctors develop new strategies to better diagnose, monitor, and treat brain tumors.

Cerebrospinal Fluid Biomarkers for Brain Tumors

Cerebrospinal Fluid Biomarkers for Brain Tumors

Condition
Central Nervous System Neoplasm
Intervention / Treatment

-

Contacts and Locations

Rochester

Mayo Clinic in Rochester, Rochester, Minnesota, United States, 55905

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Any evidence of neoplasm involving the central nervous system (CNS) or its adjacent structures in contact with CSF. Such lesions may include but are not limited to intra-axial or extra-axial lesions, which could be benign, malignant or as yet undefined, involving the brain, spine, meninges, nerves, or vasculature or supporting structures
  • * Subjects must be 18 years of age or older
  • * Patients who are under 18 years of age or are a member of a vulnerable population will be excluded from this study
  • * Pregnant women or women who may be pregnant are specifically excluded from study participation
  • * Exception will be granted for patients with diminished capacity to consent if a legally authorized representative is available
  • * Patients without clinical or radiographic evidence of a potentially neoplastic CNS lesion will be excluded
  • * Patients with an inability or unwillingness of individual or legal guardian/representative to give written informed consent will be excluded
  • * Any patient for whom a clinical contraindication exists to the intended route of CSF access will be excluded. For example, a patient with a large posterior fossa mass lesion at risk of herniation, or a patient with coagulopathy, or other contraindication to lumbar puncture would not be eligible to participate via use of lumbar puncture for CSF access

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mayo Clinic,

Terence C. Burns, M.D., Ph.D., PRINCIPAL_INVESTIGATOR, Mayo Clinic in Rochester

Study Record Dates

2025-12-31