Abstract
Malignant melanoma accounts for the highest number of deaths from skin cancer, and the prognosis of patients with stage IV disease has historically been poor. Novel insights into both mutations driving tumorigenesis and immune escape mechanisms of these tumors have led to effective treatment options that have revolutionized the treatment of this disease. Targeting the MAPK kinase pathway (with BRAF and MEK inhibitors), as well as targeting checkpoints, such as cytotoxic T-lymphocyte associated protein 4 (CTLA-4) or programmed death 1 (PD-1), have improved overall survival in patients with late-stage melanoma, and biomarker research for personalized therapy is ongoing for each of these treatment modalities. In this review, we will discuss current first-line treatment options, discuss biomarkers supporting treatment decisions, and give an outlook on (combination) therapies we expect to become relevant in the near future.
MeSH terms
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Antineoplastic Combined Chemotherapy Protocols / pharmacology
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Biomarkers, Tumor / analysis*
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CTLA-4 Antigen / antagonists & inhibitors
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CTLA-4 Antigen / genetics
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Clinical Decision-Making / methods
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Humans
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Immunosuppressive Agents / pharmacology
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Immunosuppressive Agents / therapeutic use*
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MAP Kinase Signaling System / drug effects
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MAP Kinase Signaling System / genetics
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Melanoma / diagnosis
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Melanoma / drug therapy*
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Melanoma / etiology
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Melanoma / mortality
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Molecular Targeted Therapy / methods
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Molecular Targeted Therapy / trends
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Neoplasm Staging
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Prognosis
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Programmed Cell Death 1 Receptor / antagonists & inhibitors
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Programmed Cell Death 1 Receptor / genetics
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Protein Kinase Inhibitors / pharmacology
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Protein Kinase Inhibitors / therapeutic use
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Skin Neoplasms / diagnosis
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Skin Neoplasms / drug therapy*
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Skin Neoplasms / etiology
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Skin Neoplasms / mortality
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Treatment Outcome
Substances
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Biomarkers, Tumor
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CTLA-4 Antigen
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CTLA4 protein, human
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Immunosuppressive Agents
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PDCD1 protein, human
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Programmed Cell Death 1 Receptor
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Protein Kinase Inhibitors