Cerebrospinal Fluid Biomarkers for Brain Tumors

Overview

About this study

The purpose of this study is to help generate a repository of Cerebrospinal  Fluid (CSF) samples relevant to neuro-oncology research that may facilitate the identification of biomarkers that are predictive of disease burden, therapeutic susceptibility or response to therapy. This protocol will also provide a vehicle for CSF access for patients or providers wishing to generate or evaluate individualized biomarkers as part of other research or individualized therapy protocols.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adult patients (≥ 18 years).
  • Known or suspected brain tumor.
  • Willing and able to consent to a research-only procedure for Cerebrospinal  Fluid (CSF) collection.

Exclusion Criteria:

  • Patients < 18 years old.
  • Member of a vulnerable population.
  • Unable to provide written, informed consent.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Terence Burns, M.D., Ph.D.

Open for enrollment

Contact information:

Lucas Carlstrom M.D., Ph.D.

(507) 284-2816

Carlstrom.Lucas@mayo.edu

More information

Publications

Publications are currently not available