作者: Javier Munoz
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摘要: Vemurafenib has been approved in the United States for treatment of relapsed or refractory BRAF mutation positive malignant melanoma and is being investigated various other malignancies. The RAS/RAF/MEK/ERK (MAPK) pathway critical to cell proliferation many human cancers. mTOR inhibitors are well known exert profound anticancer effects across malignancies through inhibition PTEN/PI3K/AKT/mTOR (mTOR) pathway. We hypothesize that toxicity profile combination vemurafenib everolimus will be tolerated. primary objective find maximum tolerated dose (MTD) following a standard 3 + design. most common diagnosis was 5 out 10 patients