Abstract
Metastatic thymic carcinoma is an aggressive neoplasm for which multimodal therapies are often ineffective. We describe here a heavily pretreated patient with advanced thymic carcinoma responsive to multikinases inhibitor BAY 43-9006 (Sorafenib). Of note, a hitherto unreported c-kit missense mutation on exon 17 (D820E) identified in tumor cells seems to explain the clinical response and highlight the key role of molecular analysis in predicting efficacy of targeted therapies even in thymic neoplasms.
MeSH terms
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Base Sequence
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Benzenesulfonates / therapeutic use*
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Humans
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Male
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Middle Aged
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Molecular Sequence Data
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Mutation, Missense / genetics
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Niacinamide / analogs & derivatives
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Phenylurea Compounds
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Protein Kinase Inhibitors / therapeutic use*
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Proto-Oncogene Proteins c-kit / genetics
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Pyridines / therapeutic use*
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Receptors, Vascular Endothelial Growth Factor / antagonists & inhibitors
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Sorafenib
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Thymoma / drug therapy*
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Thymoma / genetics
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Thymoma / secondary
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Thymus Neoplasms / drug therapy*
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Thymus Neoplasms / genetics
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Thymus Neoplasms / secondary
Substances
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Benzenesulfonates
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Phenylurea Compounds
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Protein Kinase Inhibitors
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Pyridines
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Niacinamide
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Sorafenib
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Proto-Oncogene Proteins c-kit
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Receptors, Vascular Endothelial Growth Factor