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METHODS FOR THE PREDICTION OF A PERSONALIZED ESA-DOSE IN THE TREATMENT OF ANEMIA

机译:个体化ESA剂量在贫血治疗中的预测方法

摘要

The present invention pertains to the use of an Integrative pharmacokinetic/pharmacodynamic (PK/PD) ESA-EpoR mathematical model for calculating the binding behaviour of erythropoiesis stimulating agents (ESA). The invention provides methods for the determining of ESA binding sites in cells or patients suffering from anemia. Knowing the amount of ESA binding sites enables the clinical practitioner to optimize the dosage regimen during a treatment of anemia, in particular in patients suffering from a cancerous disease. Further provided are methods for screening ESAs which have a higher specificity for cells strongly expressing the EPO receptor such as colony forming units-erythroid (CFU-E) cells, and not to cells with a low level of EPO receptor cell surface expression, which is the case in cancer cells. Also provided is a computer implemented method, comprising the use of the mathematical model of the invention.
机译:本发明涉及综合药代动力学/药效学(PK / PD)ESA-EpoR数学模型在计算红细胞生成刺激剂(ESA)的结合行为中的用途。本发明提供了确定患有贫血的细胞或患者中ESA结合位点的方法。知道ESA结合位点的量使临床医生能够在贫血治疗期间,特别是在患有癌性疾病的患者中,优化剂量方案。进一步提供了筛选ESA的方法,其对强烈表达EPO受体的细胞如集落形成单位-类红细胞(CFU-E)细胞具有较高的特异性,而对具有低EPO受体细胞表面表达水平的细胞不具有较高的特异性。癌细胞中的情况。还提供了一种计算机实现的方法,包括使用本发明的数学模型。

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