
Sorafenib inhibits multiple kinases involved in angiogenesis and tumour growth. It is used for second-line treatment of advanced kidney cancer and some forms of liver cancer. A placebo-controlled trial in 80 patients with metastatic kidney cancer showed a statistically significant increase in muscle loss during sorafenib therapy. Skeletal muscle mass fell by about 5% after 6 months of treatment and by 8% after one year. In practice, patients treated with sorafenib should be assessed for muscle wasting. The clinical consequences of muscle wasting--loss of autonomy and walking difficulties--should be considered when weighing the benefits and harms of sorafenib therapy.
Niacinamide, Indoles, Pyridines, Phenylurea Compounds, Benzenesulfonates, Sorafenib, Piperazines, Rhabdomyolysis, Pyrimidines, Benzamides, Imatinib Mesylate, Sunitinib, Humans, Pyrroles, Muscle, Skeletal, Protein Kinase Inhibitors
Niacinamide, Indoles, Pyridines, Phenylurea Compounds, Benzenesulfonates, Sorafenib, Piperazines, Rhabdomyolysis, Pyrimidines, Benzamides, Imatinib Mesylate, Sunitinib, Humans, Pyrroles, Muscle, Skeletal, Protein Kinase Inhibitors
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