Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT03741673

Pre-operative SRS or Post-operative SRS in Treating Cancer Patients With Brain Metastases

Led by M.D. Anderson Cancer Center · Updated on 2025-09-05

180

Participants Needed

1

Research Sites

429 weeks

Total Duration

On this page

Sponsors

M

M.D. Anderson Cancer Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This phase III trial studies stereotactic radiosurgery (SRS) before surgery to see how well it works compared with SRS after surgery in treating patients with cancer that has spread to the brain (brain metastases). SRS is the delivery of focused, high-dose radiation given in a single session to the tumors, with a minimal dose given to uninvolved areas of the brain.

CONDITIONS

Official Title

Pre-operative SRS or Post-operative SRS in Treating Cancer Patients With Brain Metastases

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • The primary brain lesion before surgery can be up to 4 cm for single fraction SRS or up to 7 cm for multifraction therapy
  • Patients must be candidates for stereotactic radiosurgery within 30 days before or after surgical removal of brain tumors
  • Patients must have a Karnofsky performance score of 70 or higher or an ECOG score of 2 or less within 30 days before enrollment
  • Patients must agree to randomization and sign informed consent
  • No signs of leptomeningeal disease on brain imaging reviewed by specialists
  • Must have a documented history of cancer
Not Eligible

You will not qualify if you...

  • Patients who have had prior radiation therapy to the brain
  • Patients with primary tumors that are small-cell lung cancer, lymphoma, leukemia, or multiple myeloma
  • Pregnant or breastfeeding women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

D

Debra Yeboa

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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