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PROGNOSTIC GROUPING OF OVARIAN CANCER PATIENTS

机译:卵巢癌患者的预后分组

摘要

The present invention relates to molecular profiling in order to identify clinically applicable biomarkers for stratifying cancer patients having different responses to a certain therapy. Specifically, the present invention provides clinically applicable methods and means for predicting the response to the platinum and taxane combination therapy in cancer patients, especially in high-grade serous ovarian cancer (HGS-OvCa) and basal like breast cancer (BL-BrCa) patients. The method of the invention comprises determining the set of biomarkers in patient samples obtained from patients suffering from HGS-OvCa; and determining outcome groups for cancer patients based on the expression of the set of biomarkers. A panel of biomarkers and a kit is also provided. The invention provides substantial help in the clinical decision making and is especially useful in the selection of first line chemotherapy regimen.
机译:本发明涉及分子谱分析,以鉴定用于对对某种疗法具有不同反应的癌症患者进行分层的临床上可应用的生物标志物。具体地,本发明提供了在癌症患者中,特别是在高度浆液性卵巢癌(HGS-OvCa)和基底样乳腺癌(BL-BrCa)患者中预测对铂和紫杉烷联合疗法的反应的临床适用方法和手段。 。本发明的方法包括确定得自患有HGS-OvCa的患者的患者样品中的一组生物标记;并根据该组生物标志物的表达确定癌症患者的结局组。还提供了一组生物标志物和试剂盒。本发明在临床决策中提供了实质性帮助,并且在选择一线化疗方案中特别有用。

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