首页> 外国专利> METHOD FOR DETERMINING RISK OF DEVELOPING PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA, AND COMPOSITION FOR TREATING PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA

METHOD FOR DETERMINING RISK OF DEVELOPING PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA, AND COMPOSITION FOR TREATING PRIMARY CENTRAL NERVOUS SYSTEM LYMPHOMA

机译:确定发展为原发性中枢神经系统淋巴瘤的风险的方法,以及治疗原发性中枢神经系统淋巴瘤的组合物

摘要

The purpose of the present invention is to provide a method for easily determining the risk of developing primary central nervous system lymphoma, and a composition for treating primary central nervous system lymphoma. The present invention solves the above problem through: a method for determining the risk of a human subject developing primary central nervous system lymphoma, wherein the method includes a step for detecting mutant variants of GRB2 and/or MYD88, or nucleic acids that encode these mutant variants, from a sample derived from the subject, and a step for determining that there is a high risk of the subject developing primary central nervous system lymphoma when the abovementioned mutant variants or nucleic acids encoding the mutant variants are detected; and a composition for treating primary central nervous system lymphoma in a human subject, wherein the composition includes rituximab, or an agent for inhibiting the activity of GRB2 and/or a downstream signaling factor thereof, in the MAPK pathway, taking the abovementioned mutant variants to be the cause of primary central nervous system lymphoma.
机译:本发明的目的是提供一种易于确定发生原发性中枢神经系统淋巴瘤的风险的方法,以及一种用于治疗原发性中枢神经系统淋巴瘤的组合物。本发明通过以下方法解决了上述问题:用于确定人类受试者发展原发性中枢神经系统淋巴瘤的风险的方法,其中该方法包括检测GRB2和/或MYD88的突变体变体或编码这些突变体的核酸的步骤。当检测到上述突变体变体或编码该突变体变体的核酸时,确定来自受试者的样品中的变体,以及确定该受试者发生原发性中枢神经系统淋巴瘤的高风险的步骤;以及在人类受试者中治疗原发性中枢神经系统淋巴瘤的组合物,其中所述组合物在上述MAPK途径中包含利妥昔单抗或其抑制剂GRB2和/或其下游信号传导因子的活性,并采用上述突变体变体作为载体。是原发性中枢神经系统淋巴瘤的病因。

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