Abstract
Vascular endothelial growth factor (VEGF) is, to date, the key element in the pathogenesis of renal cell carcinoma (RCC). VEGF pathway activation is responsible for the recruitment, migration, and expansion of endothelial cells, with this angiogenesis tumor model being characteristic of RCC. Different strategies have been developed for almost a decade to block the VEGF pathway in this setting. Four different compounds were approved for metastatic RCC (mRCC) in the past 6 years: bevacizumab, sunitinib, sorafenib, and pazopanib. Axitinib and tivozanib are also promising compounds under evaluation. The revolution in the management and prognosis of patients with mRCC is ongoing.
Copyright © 2011 Elsevier Inc. All rights reserved.
MeSH terms
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Angiogenesis Inhibitors / therapeutic use
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Antibodies, Monoclonal, Humanized / therapeutic use*
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Benzenesulfonates / therapeutic use
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Bevacizumab
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Carcinoma, Renal Cell / drug therapy*
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Carcinoma, Renal Cell / metabolism
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Carcinoma, Renal Cell / pathology
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Clinical Trials as Topic
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Humans
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Kidney Neoplasms / drug therapy*
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Kidney Neoplasms / metabolism
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Kidney Neoplasms / pathology
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Models, Biological
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Niacinamide / analogs & derivatives
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Phenylurea Compounds
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Pyridines / therapeutic use
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Receptors, Vascular Endothelial Growth Factor / antagonists & inhibitors
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Receptors, Vascular Endothelial Growth Factor / metabolism
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Sorafenib
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Vascular Endothelial Growth Factor A / antagonists & inhibitors*
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Vascular Endothelial Growth Factor A / metabolism
Substances
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Angiogenesis Inhibitors
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Antibodies, Monoclonal, Humanized
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Benzenesulfonates
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Phenylurea Compounds
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Pyridines
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VEGFA protein, human
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Vascular Endothelial Growth Factor A
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Niacinamide
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Bevacizumab
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Sorafenib
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Receptors, Vascular Endothelial Growth Factor