Forty mCRC specimens harboring KRAS, NRAS, BRAF, and/or PIK3CA mutations were implanted in nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice....When correlating such drug sensitivity subgroups to the distribution of mutant genotypes, we found that the 3 BRAF codon 600 mutant tumors seem to be poorly sensitive to MEK inhibition and all segregated in the subset that showed preferential responsiveness to BEZ235.