Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT01891318

Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study

Led by Case Comprehensive Cancer Center · Updated on 2026-05-08

36

Participants Needed

2

Research Sites

686 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This Phase I/II trial studies the ability to stop brain metastases from coming back after treatment with radiosurgery followed by surgical resection. It will also evaluate the side effects of these combined treatments and help determine the best radiosurgery dose. Radiosurgery focuses the x-rays directly to the tumor and cause less damage to the normal tissue in the brain.

CONDITIONS

Official Title

Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a prior histologic diagnosis of cancer other than small cell lung cancer, lymphoma, and germ cell histologies
  • Have MRI evidence of 1 to 4 brain metastases, with at least one lesion larger than 20 mm and up to 50 mm in maximal diameter suitable for radiosurgery and complete surgical removal
  • All other brain metastases must be suitable for radiosurgery
  • May have had prior radiosurgery to lesions other than the one planned for neoadjuvant radiosurgery and resection
  • Have a Karnofsky performance score of 70 or higher
Not Eligible

You will not qualify if you...

  • Medically unfit to undergo surgical removal of brain metastasis
  • Prior whole brain radiotherapy
  • Contraindication for MRI imaging
  • Unable to participate due to physical or mental limitations
  • Unable or unwilling to attend all required follow-up visits
  • Unable to safely deliver 10 Gray or less to optic nerve/chiasm at planning
  • Tumor located in the brainstem
  • Imaging or cytologic evidence of leptomeningeal disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center

Cleveland, Ohio, United States, 44106

Withdrawn

2

Cleveland Clinic, Case Comprehensive Cancer Center

Cleveland, Ohio, United States, 44195

Actively Recruiting

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Research Team

E

Erin Murphy, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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