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RecruitingLast updated: 10 October 2025

BrainPOP Precision: This study aims to improve treatment outcomes for people with central nervous system (CNS) tumours by using real-time molecular profiling to guide personalised care throughout diagnosis, treatment, and recurrence.Evaluating the feasibility and impact of the implementation of precision medicine into the care of patients with brain cancers

Trial purpose

Medical clipboardDiagnostic

Tumor type

Brain and Spinal Cancers Brain and Spinal

Age

People18+

Trial acronym

BrainPOP Precision

Clinical summary

Summary

This study involves real-time molecular profiling of brain or other central nervous system (CNS) tumours by analysing tissue, cerebrospinal fluid (CSF), and blood plasma at critical points throughout cancer diagnosis, treatment, and recurrence. Molecular profiling is like taking a detailed snapshop of a tumour's genetic makeup, helping doctors identify specific changes or mutations to guide effective treatment choices.

You may be eligible for this study if you are aged 18 or older with a known or strong suspicion of primary CNS cancer, suitable for systemic treatment. 

Biospecimens including tumour tissue, blood and CSF will be collected longitudinally from participants during routine care procedures and/or by accessing stored material. Clinical data will be collected throughout the study. Biospecimens collected will be molecularly profiled.

Molecular profiling analysis will include targeted panel sequencing, whole genome transcriptome sequencing and methylation array using tumour tissue samples. Results will be returned to the treating clinicians, accompanied by interpretation and recommendations from the molecular tumour board. By integrating clinical, molecular, histopathological, and radiological data, the project seeks to improve patient outcomes and establish feasability of molecular profiling in CNS tumours. 

https://www.thebraincancercentre.org.au/

Conditions

This trial is treating people with a known or strong clinical suspicion of primary central nervous system cancer

Eligibility

Inclusion

1. Patients with known, or strong clinical suspicion, of primary CNS cancer.
2. The patient, or patient’s parent/guardian, has given written informed
consent (and assent, as applicable)
3. Suitable for systemic treatment.
4. ECOG (Eastern Cooperative Oncology Group) performance status less than or equal to 2
5. Estimate life expectancy greater than 6 months.
6. Access to appropriate sample(s) for molecular testing.

Exclusion

1. Unable to provide informed consent.

Inclusion

  • You have the type of cancer, symptoms, or health risks that this clinical trial is focused on.
Message

Clinical trials have complex eligibility criteria, and other criteria may apply for this trial. Ask your doctor about whether this trial could be right for you.

Participating hospitals

Recruiting hospitals

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Trial Identifiers

Information on this page is partially produced from ANZCTR *. View further details about this trial on the registry via the links below:

Trial sponsor

Walter and Eliza Hall Institute of Medical Research

Scientific Title

Evaluating the feasibility and impact of the implementation of precision medicine into the care of patients with brain cancers

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