Clinical Trials Directory

Trials / Completed

CompletedNCT00983359

Stereotactic Radiation Therapy in Treating Patients With Brain Metastases

A Phase II Trial of Focal Therapy in the Treatment of Patients With 1-3 Brain Metastases

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Ohio State University Comprehensive Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Stereotactic radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue. PURPOSE: This phase II trial is study how well stereotactic radiation therapy works in treating patients with brain metastases

Detailed description

OBJECTIVES: Primary * To determine the neurological death rate following the initiation of conformal stereotactic radiotherapy in patients with 1-3 brain metastases. Secondary * To determine the overall survival rate at 6 months. * To determine the progression-free survival rate or brain metastases recurrence rate at 6 months. * To determine the time to neurological death, time to systemic death, and Karnofsky decay time. * To determine the frequency and severity of adverse events associated with conformal stereotactic radiotherapy. OUTLINE: Patients undergo conformal stereotactic radiotherapy over 5 days to an area including 3 mm around the metastases or the surgical cavity. Patients may receive additional radiotherapy if symptomatic metastases emerge at different sites. After completion of study treatment, patients are followed up at 1 and 2 months and then every 3 months thereafter.

Conditions

Interventions

TypeNameDescription
RADIATIONRadiation TherapyPatients undergo conformal stereotatic radiation therapy QD (every day) over 5 days.

Timeline

Start date
2007-04-01
Primary completion
2012-08-01
Completion
2012-08-01
First posted
2009-09-24
Last updated
2017-06-06
Results posted
2016-06-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00983359. Inclusion in this directory is not an endorsement.