BRIANSTORM - Early Identification of Patients With Brain Metastases

NCT ID: NCT05185557

Last Updated: 2023-02-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-08-16

Study Completion Date

2025-02-28

Brief Summary

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A single arm observational study investigating the incidence of brain metastasis in patients with cancer recti and lung metastasis

Detailed Description

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In this study the investigators want to investigate the incidence of brain metastasis in a selected high-risk group of patients with metastatic colorectal cancer. Possible prognostic biological aspects will be investigated by translational analysis of biological samples. The study population consists of patients with metastatic rectal cancer and presence of lung metastasis. The patients will undergo a standard MRI scan of the brain including injection of intravenous contrast. If positive finding, images will be evaluated at the multidisciplinary tumor board for potential treatment options according to clinical practice. Standard follow-up program is followed, as per clinical practice. If the initial MRI scan of cerebrum detects brain metastasis this will be treated and followed as per clinical practice. Translational blood samples will be drawn at inclusion and at every imaging schedule up til 5 times

Conditions

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Metastatic Rectal Adenocarcinoma Brain Metastases

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Primary rectal tumor location

* Diagnosis of lung metastasis made by histo- or cytopathology, or by clinical and imaging criteria.
* Able to understand written information
* Consent to samples for translational research

Exclusion Criteria

* Contraindications for MRI Priorly treated or known brain metastases
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Aarhus University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Anders Kindberg Boysen

MD, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Anders K Boysen, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Department of Oncology, Aarhus University Hospital

Locations

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Department of Oncology, Aarhus University Hospital

Aarhus N, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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1-10-72-269-20

Identifier Type: -

Identifier Source: org_study_id

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