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Background








                • Multiple studies point to the MET proto-

                   oncogene as a potential driver of pRCC                                                1-3


                • Although more common in type I versus

                   type II pRCC, MET mutation and copy

                   number alteration occur in a large

                   proportion of both subtypes


                • Aim to determine if MET inhibitors could

                   improve clinical outcome relative to

                   sunitinib in patients with metastatic pRCC














                                                                            2
                 1  Cancer Genome Atlas Research Network et al N Engl J Med 2016; 374: 135–45;  Pal SK et al Eur Urol 2018; 73: 71–8; Albiges, L et al Clin Cancer Res 2014; 20:3411–21.
                 Figure Source: Fay A et al Clin Cancer Res 2014; 20: 3361–63
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