Abstract
Epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI), such as gefitinib or erlotinib, is mainly metabolized in liver. To date, the safety data on administrating EGFR-TKI to patients with liver dysfunction is quite limited. Here, we administered gefitinib to two adenocarcinoma patients with liver cirrhosis, and one patient with EGFR gene mutation in exon 21 achieved long stable disease (SD) without any toxicity. Pharmacokinetic data of alternate days administration in these patients were similar to those of daily administration in patients with normal liver function. Although further studies are needed, a reduced dose of gefitinib might be feasible for patients with liver dysfunction.
MeSH terms
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Adenocarcinoma / complications
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Adenocarcinoma / drug therapy
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Adenocarcinoma / genetics
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Antineoplastic Agents / administration & dosage
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Antineoplastic Agents / pharmacokinetics
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Antineoplastic Agents / therapeutic use*
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Carcinoma, Non-Small-Cell Lung / complications*
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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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ErbB Receptors / antagonists & inhibitors
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ErbB Receptors / genetics
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Female
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Gefitinib
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Humans
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Liver Cirrhosis / complications*
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Liver Cirrhosis / genetics
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Liver Cirrhosis / physiopathology
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Lung Neoplasms / complications*
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Lung Neoplasms / drug therapy*
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Lung Neoplasms / genetics
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Middle Aged
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Point Mutation
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Protein Kinase Inhibitors / administration & dosage
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Protein Kinase Inhibitors / pharmacokinetics
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Protein Kinase Inhibitors / therapeutic use*
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Quinazolines / administration & dosage
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Quinazolines / pharmacokinetics
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Quinazolines / therapeutic use*
Substances
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Antineoplastic Agents
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Protein Kinase Inhibitors
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Quinazolines
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ErbB Receptors
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Gefitinib