Response of Brain Metastases After Gamma-Knife Radiosurgery Using Dynamic Susceptibility-weighted Contrast-enhanced Perfusion Magnetic Resonance Imaging



Status:Active, not recruiting
Conditions:Brain Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:7/20/2016
Start Date:May 2013
End Date:May 2017

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Assessment of Early Treatment Response of Brain Metastases After Gamma-Knife Radiosurgery Using Dynamic Susceptibility-weighted Contrast-enhanced Perfusion Magnetic Resonance Imaging

This study is designed to evaluate whether advanced magnetic resonance imaging (MRI)
techniques such as dynamic susceptibility-weighted contrast-enhanced perfusion MRI may be
used to predict treatment response of brain metastasis after radiosurgery.


Inclusion Criteria:

- Patient must have newly diagnosed brain metastases visible on brain MRI. A biopsy of
the lesion is not required as long as the patient has a biopsy-proven malignancy
elsewhere and a clinician deems the lesion to be metastatic.

- At least one brain metastasis must be ≥ 1cm to allow adequate quantitative imaging
measurement for DSC-PMR.

- Patient must be clinically eligible for and elect to be treated with GK alone without
WBRT.

- Patient must be ≥ 18 years of age.

- Patient must have Karnofsky Performance Status (KPS) of at least 60

- Patient may be part of other clinical trials (as long as no other local treatments
beyond GK such as WBRT or other local therapy are indicated to the brain) or imaging
studies.

- Patient or legally authorized representative must be able to understand and willing
to sign a written informed consent document.

Exclusion Criteria:

- Patient must not have any medical contraindications to MRI (e.g., unsafe foreign
metallic implants, incompatible pacemaker, inability to lie still for long periods,
severe to end-stage kidney disease or on hemodialysis).

- Patient must not be pregnant or breastfeeding.

- Patient must not have an estimated glomerular filtration rate (eGFR) < 60
mL/min/1.73m2.

- Patient must not have melanoma.

- Patient must not have hemorrhagic lesions.
We found this trial at
1
site
St. Louis, Missouri 63108
Phone: 314-362-8516
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St. Louis, MO
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