首页> 外国专利> Method for diagnosis of prostate cancer (PCA) with a desired sensitivity in a subject; the method to monitor the progression of prostate cancer (PCA) in a subject, the method to evaluate whether a subject has to undergo a biopsy of the prostate; kit comprising a first The component and, optionally, a second component and use of a kit

Method for diagnosis of prostate cancer (PCA) with a desired sensitivity in a subject; the method to monitor the progression of prostate cancer (PCA) in a subject, the method to evaluate whether a subject has to undergo a biopsy of the prostate; kit comprising a first The component and, optionally, a second component and use of a kit

机译:在受试者中以期望的灵敏度诊断前列腺癌(PCA)的方法;监测受试者中前列腺癌(PCA)进展的方法,评估受试者是否必须进行前列腺活检的方法;包括第一组分和任选第二组分的试剂盒以及试剂盒的用途

摘要

Method for diagnosis of prostate cancer (PCA) with a desired sensitivity in a subject; the method to monitor the progression of prostate cancer (PCA) in a subject, the method to evaluate whether a subject has to undergo a biopsy of the prostate; kit comprising a first The component and, optionally, a second component and use of a kit.The invention relates to methods and kits for the diagnosis of prostate cancer (PCA) in a subject, to assess and monitor response to therapy in a subject with PCA or to monitor the progression of prostate cancer PCA based on detection of changes in the levels of expr Progress of at least a gene selected from group of PC, A3, PSMA and psgr.The invention relates also to methods for assessing whether a subject has to be subject to a biopsy of the prostate, the subject having a range of PSA in serum within 4 to 10 ng / ml.
机译:在受试者中以期望的灵敏度诊断前列腺癌(PCA)的方法;监测受试者中前列腺癌(PCA)进展的方法,评估受试者是否必须进行前列腺活检的方法;试剂盒,其包含第一组分和任选地第二组分,以及试剂盒的用途。本发明涉及用于诊断受试者的前列腺癌(PCA),评估和监测受试者对治疗的反应的方法和试剂盒。 PCA或基于检测expr水平变化来监测前列腺癌PCA的进展至少一种选自PC,A3,PSMA和psgr的基因的进展。本发明还涉及用于评估受试者是否患有前列腺癌的方法。如果要对前列腺进行活检,该受试者的血清PSA范围在4至10 ng / ml之间。

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