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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