In continuation of my update on sutent/sunitib.... 
 Pfizer Inc. announced this Tuesday that its oral multi-kinase inhibitor "Sutent" (see structure)  was determined as having a favourable benefit-risk profile by an oncology  advisory committee of the FDA for the treatment of unresectable  pancreatic neuroendocrine tumors. The panel voted 8-2 in favour of Sutent – generically called Sunitib malate.
Advanced pancreatic neuroendocrine tumour or NET, is a rare, life-threatening and difficult-to-treat form of cancer  that accounts for approximately 22-28 percent of all neuroendocrine  tumours. Nearly 90 percent of patients are initially diagnosed with  locally advanced or metastatic disease, or cancer that has spread to other organs. An unresectable tumour is one that cannot be removed or resected by surgery.
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Sutent or sunitinib malate targets vascular endothelial growth factor  receptor or VEGFR and platelet-derived growth factor receptor or PDGFR,  both of which are expressed by many types of solid tumours. The two  targets are involved in tumours acquiring blood vessels, oxygen and  nutrients needed for growth. 
Sunitinib was approved in 2006 in the United States for treating locally advanced or metastatic renal cell carcinoma  and for imatinib-refractory or -intolerant gastrointestinal stromal  tumour (GIST). It was approved for treating PNET in 2010 in Europe. A  decision on approval is expected by the end of 2011, according to a  company spokesperson....
