In people whos cancers have a PIK3CA mutation, this trial will be evaluating the drug BKM120 as a possible treatment. BKM120 works by blocking the phosphatidylinositol-3-kinase (PI3K)pathway, thereby inhibiting tumor growth and survival. The purpose of this study is to learn if the study drug BKM120 can shrink or slow the growth of your tumor. The safety of BKM120 will also be studied. Your physical state, symptoms, change in the size of your tumor, and laboratory findings obtained while you are on study will help the research team decide if BKM120 is safe and effective in patients with advanced cancers.
Subjects enrolled in this study will receive BKM120 once daily, orally, in cycles of 28 days. During Cycles 1 and 2, the following tests and procedures will be done on days 1 and 15: * physical exam * performance status * blood tests * pregnancy test (if applicable) * neuropsychiatric assessments Starting at Cycle 2 and then every other cycle thereafter (approximately every 8 weeks) tumor assessment will be performed by CT/MRI or PET scan. A chest x-ray will also be performed every 8 weeks. Beginning with Cycle 3, the following tests/procedures will be performed on Day 1 of each cycle: * physical exam * performance status * blood tests * neuropsychiatric assessments
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
100 MG PO QD in cycles of 28 days
Response Rate
Objective Response Rate (CR or PR) by RECIST 1.1 criteria
Time frame: 2 years
Clinical Benefit Rate
Clinical Benefit Rate (CR, PR, or SD) by RECIST 1.1 criteria
Time frame: 2 years
Survival
Progression Free Survival (PFS)
Time frame: 2 years
Clinical Benefit
Determine if the presence of specific co-existing mutations may influence clinical benefit from BKM120
Time frame: 2 years
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