Abstract
Therapy for advanced non-small-cell lung cancer has developed significantly with new awareness of histologic subtype as an important factor in guiding treatment and the development of targeted agents for molecular subgroups harboring critical mutations that spur on cancer growth. In this comprehensive review, we look back at developments in targeted therapy for advanced non-small-cell lung cancer, reviewing in detail efforts, both successful and in some cases less so, to target EGFR, VEGF and ALK. This review provides an overview of where the field stands at present and the areas we feel are most likely to provide challenges and potential successes in the next 5 years including immune checkpoint inhibition, epigenetic therapy and driver mutation targeting.
MeSH terms
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Anaplastic Lymphoma Kinase
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Carcinoma, Non-Small-Cell Lung / drug therapy*
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Carcinoma, Non-Small-Cell Lung / genetics
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Carcinoma, Non-Small-Cell Lung / pathology
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Crizotinib
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Drug Resistance, Neoplasm
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Epigenesis, Genetic
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ErbB Receptors / genetics
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Humans
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Lung Neoplasms / drug therapy*
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Lung Neoplasms / genetics
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Lung Neoplasms / pathology
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Molecular Targeted Therapy / methods*
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Mutation
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Protein Kinase Inhibitors / pharmacology
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Protein Kinase Inhibitors / therapeutic use
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Protein Transport / drug effects
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Pyrazoles / pharmacology
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Pyridines / pharmacology
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Receptor Protein-Tyrosine Kinases / metabolism
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Vascular Endothelial Growth Factor A / antagonists & inhibitors
Substances
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Protein Kinase Inhibitors
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Pyrazoles
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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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Crizotinib
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ALK protein, human
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Anaplastic Lymphoma Kinase
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EGFR protein, human
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ErbB Receptors
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Receptor Protein-Tyrosine Kinases