RecruitingNot ApplicableNCT07476781

CSF and Blood Plasma Liquid Biopsy in Patients With Metastatic Solid Tumours and CNS Metastases or no CNS Metastases

Exploring the Feasibility of Cerebrospinal Fluid (CSF) Liquid Biopsy in Patients With Metastatic Solid Tumours and Leptomeningeal Disease (Cohort A), Parenchymal Brain Metastases (Cohort B), or No Evidence of Central Nervous System (CNS) Metastases (Cohort C): A Pilot Study


Sponsor

Sunnybrook Health Sciences Centre

Enrollment

60 participants

Start Date

Dec 12, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective, single-centre feasibility study of CSF ctDNA conducted at the Sunnybrook Odette Cancer Centre (SOCC), Toronto, Canada, including multiple solid tumor, stratified into cohorts according to CNS disease involvement, including leptomeningeal disease (Cohort A), parenchymal brain metastases (Cohort B), and no evidence of CNS metastases (Cohort C).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is collecting spinal fluid (CSF) and blood samples from patients with metastatic cancer — particularly those whose cancer has spread to the brain or the lining of the brain and spinal cord (called leptomeningeal disease) — to develop and test liquid biopsy tools. These tests look for DNA shed by tumors in body fluids, which could help doctors track cancer activity without needing invasive procedures. **You may be eligible if...** - You have a solid tumor cancer that has spread (metastatic), AND you fall into one of these groups: - Your cancer has spread to the lining of the brain or spinal cord (leptomeningeal disease) - Your cancer has spread to the brain itself (brain metastases) - Your cancer has spread elsewhere in the body but NOT to the brain or spinal cord - You are able to safely have a lumbar puncture (spinal tap) or have an accessible Ommaya reservoir **You may NOT be eligible if...** - You are unable or unwilling to give written consent (translators are allowed) - You have conditions that make a lumbar puncture unsafe (e.g., blood clotting problems, low platelet count, infection at the puncture site, significant brain pressure) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREOne time CSF and blood sample

One-time CSF collective via lumbar puncture or Ommaya reservoir and collection of concurrent plasma of peripheral blood (liquid biopsy).


Locations(1)

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

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NCT07476781


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