Abstract
Axitinib is an oral inhibitor of the VEGF, PDGF and colony stimulating factor-1 receptor tyrosine kinases and is currently in development by Pfizer Inc for the potential treatment of various solid tumors. Phase II trials with this agent alone or in combination with chemotherapeutic drugs were reported in several types of malignancy, with activity observed in thyroid, pancreatic, lung, renal, breast and colorectal cancers, melanoma and other carcinomas. Although frequent side effects have included fatigue, hypertension, diarrhea, hand-foot syndrome and proteinuria, axitinib was well tolerated overall. Larger, randomized phase II/III studies were ongoing at the time of publication.
MeSH terms
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Angiogenesis Inhibitors / adverse effects
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Angiogenesis Inhibitors / metabolism
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Angiogenesis Inhibitors / pharmacokinetics
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Angiogenesis Inhibitors / pharmacology
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Angiogenesis Inhibitors / therapeutic use*
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Angiogenesis Inhibitors / toxicity
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Animals
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Axitinib
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Clinical Trials, Phase I as Topic
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Clinical Trials, Phase II as Topic
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Clinical Trials, Phase III as Topic
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Contraindications
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Humans
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Imidazoles / adverse effects
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Imidazoles / metabolism
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Imidazoles / pharmacokinetics
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Imidazoles / pharmacology
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Imidazoles / therapeutic use*
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Imidazoles / toxicity
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Indazoles / adverse effects
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Indazoles / metabolism
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Indazoles / pharmacokinetics
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Indazoles / pharmacology
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Indazoles / therapeutic use*
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Indazoles / toxicity
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Neoplasms / drug therapy*
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Patents as Topic
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Randomized Controlled Trials as Topic
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Structure-Activity Relationship
Substances
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Angiogenesis Inhibitors
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Imidazoles
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Indazoles
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Axitinib