首页> 外国专利> methods to determine the effectiveness of a selective treatment of epidermal growth factor receptor in a patient, to treat a patient and to select a compound that inhibits the catalytically kinase activity of a variant epidermal growth factor receptor, probe, kit, compound that inhibits the catalytically kinase activity of a variant epidermal growth factor receptor, pharmaceutical composition, nucleic acid and isolated protein

methods to determine the effectiveness of a selective treatment of epidermal growth factor receptor in a patient, to treat a patient and to select a compound that inhibits the catalytically kinase activity of a variant epidermal growth factor receptor, probe, kit, compound that inhibits the catalytically kinase activity of a variant epidermal growth factor receptor, pharmaceutical composition, nucleic acid and isolated protein

机译:确定选择性治疗患者中表皮生长因子受体的有效性,治疗患者并选择抑制变体表皮生长因子受体的催化激酶活性的化合物的方法,探针,试剂盒,抑制催化作用的化合物表皮生长因子受体变体的激酶活性,药物组合物,核酸和分离的蛋白质

摘要

METHODS FOR DETERMINING THE POSSIBILITY OF EFFECTIVENESS OF A SELECTIVE EPIDERMIC GROWTH FACTOR RECEPTOR TREATMENT IN A PATIENT, TO TREAT A PATIENT AND TO SELECT A COMPOUND THAT INHIBITS THE CATALYTIC ACTIVITY OF A RECEIVER SON RECEPTOR CINASE, KIT, COMPOUND THAT INHIBITS CATALYTIC ACTIVITY OF KINASE OF A VARIANT EPIDERMIC GROWTH FACTOR RECEIVER, PHARMACEUTICAL COMPOSITION, NUCLEIC ACID AND PROTEIN ISOLATED. The present invention relates to a method for determining cancer responsiveness to an epidermal growth factor receptor (EGFR) treatment. In a preferred embodiment, the presence of at least one variance in the kinase domain of the erbB | confers sensitivity to the gefitinib tyrosine kinase inhibitor. Thus, a diagnostic assay for these changes will allow the administration of gefitinib, erlotinib and other tyrosine synase inhibitors to those patients most likely responsive to the drug.
机译:确定一种选择性的表皮生长因子受体治疗的患者的有效性的可能性的方法,以治疗患者和选择一种化合物,以抑制在受体激酶,激酶,蛋白激酶,蛋白激酶,免疫球蛋白的表达各种表皮生长因子受体,药物组成,核酸和蛋白质均已分离。本发明涉及确定对表皮生长因子受体(EGFR)治疗的癌症反应性的方法。在一个优选的实施方案中,erbB |的激酶结构域中存在至少一个变异。赋予吉非替尼酪氨酸激酶抑制剂敏感性。因此,针对这些变化的诊断测定将允许将吉非替尼,厄洛替尼和其他酪氨酸合酶抑制剂给予最可能对该药物有反应的患者。

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