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      Molecular basis for sunitinib efficacy and future clinical development.

      Nature reviews. Drug discovery
      Angiogenesis Inhibitors, adverse effects, pharmacology, therapeutic use, Animals, Clinical Trials as Topic, Drug Design, Drug Resistance, Neoplasm, Humans, Indoles, Neoplasms, blood supply, drug therapy, enzymology, metabolism, Protein-Tyrosine Kinases, antagonists & inhibitors, Pyrroles, Receptors, Vascular Endothelial Growth Factor, biosynthesis, Vascular Endothelial Growth Factor A

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          Abstract

          Sunitinib malate (SU11248/Sutent; Pfizer) is a multitargeted tyrosine kinase inhibitor that has potent anti-angiogenic and antitumour activities. Definitive efficacy has been demonstrated in advanced renal cell carcinoma and in gastrointestinal stromal tumours that are refractory or intolerant to imatinib (Gleevec; Novartis), which has provided the basis for the recent regulatory approvals for these indications. This article summarizes the discovery and development of sunitinib, and discusses key issues for the multitargeted approach in cancer treatment, such as markers of response and development of resistance, and their significance for the future development of sunitinib and other multikinase inhibitors.

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