The purpose of this study is to determine the maximum tolerated dose (MTD) of vorinostat given concurrently with stereotactic radiosurgery (SRS) to treat non-small cell lung cancer (NSCLCA) brain metastases in patient with 1-4 lesions.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
17
Orally up to 400 mg
Single fraction stereotactic radiotherapy - Standard of Care
Stanford University School of Medicine
Stanford, California, United States
Moffitt Cancer Center
Tampa, Florida, United States
The maximum tolerated dose of vorinostat with concurrent radiosurgery will be determined.
Time frame: 30 days following Stereotactic Radiosurgery
During the expanded phase I portion of the study, the safety of the Maximum tolerated dose dose will be confirmed.
Time frame: 30 days following Stereotactic Radiosurgery
The radiologic response, defined as local control and distant intra-cranial control rates at 3-months following radiotherapy, will be determined.
Time frame: 3 months following Stereotactic Radiosurgery
The short-term (< 30 days post-treatment) and long-term (> 30 days post-treatment) adverse effects will be determined.
Time frame: 12 months
The 12-month survival rate from the date of Stereotactic Radiosurgery will be determined.
Time frame: 12 months
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