2.1
Bevacizumab (Avastin, Roche) is a humanised monoclonal antibody that inhibits both vascular endothelial growth factor (VEGF)-induced signalling and VEGF-driven angiogenesis. This reduces vascularisation of tumours, thereby inhibiting tumour growth. Bevacizumab is administered by intravenous infusion. Bevacizumab in combination with carboplatin and gemcitabine has a marketing authorisation for 'treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor-targeted agents'. The licensed dose of bevacizumab is 15 mg/kg of body weight given once every 3 weeks in combination with carboplatin and gemcitabine for 6 cycles and up to 10 cycles, followed by continued use of bevacizumab as single agent until disease progression.