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Pre- Versus Post-operative SRS for Resectable Brain Metastases

A Randomized Controlled Trial of Pre-operative Versus Post-operative Stereotactic Radiosurgery for Patients With Surgically Resectable Brain Metastases

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04474925
Enrollment
8
Registered
2020-07-17
Start date
2021-09-27
Completion date
2025-04-07
Last updated
2025-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Metastases

Keywords

Neurosurgery, Stereotactic Radiosurgery

Brief summary

The purpose of this study is to determine if performing radiotherapy (SRS) prior to surgery results in better treatment outcomes than performing surgery before radiotherapy for patients with brain metastases. Brain metastases occur when cancer cells from a primary cancer (e.g. lung, breast, colon) travel through the bloodstream and spread (metastasize) to the brain. As these new tumors grow they apply pressure and change how healthy brain tissue works. This can lead to a loss of brain function and worsening quality of life. Treatments for patients whose cancer has spread to the brain is often surgery, radiation therapy (radiotherapy) or a combination of both. Surgery is one the main treatments for brain tumors. To remove the tumor, a neurosurgeon makes an opening in the skull and attempts to the remove the entire tumor. If the tumor is too close to important brain tissue, the surgeon may attempt to remove part of the tumor. Removal of the tumor from the brain tissue is called resection. The complete or partial removal of tumor helps to relieve symptoms by reducing pressure on healthy tissues and reduces the amount of tumor that needs to be treated by radiotherapy. One type of radiotherapy used to treat brain metastases is stereotactic radiosurgery (SRS). SRS uses many focused radiation beams to treat tumors within the brain. Unlike surgery, there is no incision or cut being made. Instead, SRS uses an accurate map of your brain to deliver a precise beam of radiation to the tumors. The radiation damages the tumor cells forcing them to shrink and die off. The focused radiation beams also limit damage to healthy brain tissue minimizing side effects. Surgery followed by radiotherapy is a standard treatment for brain metastases. However, there are still risks associated with the combination of treatments. This study plans to investigate whether performing surgery prior to SRS results in improved quality of life and decreased side effects.

Interventions

RADIATIONStereotactic Radiosurgery

SRS uses many focused radiation beams to treat tumors within the brain

PROCEDUREBrain Surgery

Surgery to remove brain metastases

Sponsors

AHS Cancer Control Alberta
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Pathologically-proven primary malignancy * ECOG 0-2 * Ability to complete neurocognitive testing without assistance from family or friends. * Previous SRS to lesions other than the one being resected is allowed * Patients of childbearing / reproductive potential must have a negative urine or serum pregnancy test ≤7 days before enrollment * Participants capable of giving informed consent, or if appropriate participants having an acceptable individual capable of giving consent

Exclusion criteria

* Patients who have received prior WBRT, or SRS to the lesion being resected at time of study accrual * Patients unable to undergo MRI scan (e.g. pacemaker) * Leptomeningeal disease * Germ cell tumor, small cell lung cancer or hematological primary malignancy

Design outcomes

Primary

MeasureTime frameDescription
Local ControlThis will be assessed at 12 monthsTo compare local control (in months) of pre-operative versus post-operative SRS

Secondary

MeasureTime frameDescription
Trial Making TestsThis will be assessed at 3,6,9,12,16 and 24 months.Participants are scored on their ability to complete the test within a certain timeframe.
Local ControlThis will be assessed at 6 and 24 months.To compare local control (in months) of pre-operative versus post-operative SRS
Distant Brain Recurrence RateThis will be assessed at 6,12 and 24 months.To compare Distant Brain Recurrence Rate (%) of pre-operative versus post-operative SRS
Controlled Oral Word AssociationThis will be assessed at 3,6,9,12,16 and 24 months.Participants are scored on their ability to generate words starting with a specific letter in a one minute timeframe.
Overall SurvivalThis will be assessed at 6,12 and 24 months.Overall survival will be compared between both treatment arms
Hopkins Verbal Learning TestThis will be assessed at 3,6,9,12,16 and 24 months.Participants are scored using a points based system on Total Recall, Delayed Recall, Retention (% retained), and a Recognition Discrimination Index.
Leptomeningeal Recurrence RateThis will be assessed at 6,12 and 24 months.To compare the Leptomeningeal Recurrence Rate (%) of pre-operative versus post-operative SRS

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026