Abstract
The treatment of metastatic melanoma has progressed greatly during the last two years. Nowadays melanomas can be divided into molecular subgroups, this being therapeutically relevant. Around 60% of melanomas show a BRAF mutation and can be treated with selected tyrokinase inhibitors. In addition a CTLA-4-antibody was developed which shuts off the natural immune breaking system resulting in a continuous anti-tumor reaction. Angiogenesis inhibitors have shown there importance in different phase II trials. We hope that this represents only the first step of an individualized treatment for metastatic melanoma.
MeSH terms
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Angiogenesis Inhibitors / adverse effects
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Angiogenesis Inhibitors / therapeutic use
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Antibodies, Monoclonal / adverse effects
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Antibodies, Monoclonal / therapeutic use*
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Antibodies, Monoclonal, Humanized
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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CTLA-4 Antigen / antagonists & inhibitors
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Forecasting
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Humans
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Indoles / adverse effects
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Indoles / therapeutic use
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Ipilimumab
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Melanoma / drug therapy*
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Melanoma / mortality
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Melanoma / secondary*
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Molecular Targeted Therapy / adverse effects
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Molecular Targeted Therapy / trends*
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Skin Neoplasms / drug therapy*
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Skin Neoplasms / mortality
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Sulfonamides / adverse effects
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Sulfonamides / therapeutic use
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Survival Rate
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Vemurafenib
Substances
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Angiogenesis Inhibitors
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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CTLA-4 Antigen
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Indoles
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Ipilimumab
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Sulfonamides
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Vemurafenib
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tremelimumab