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Improved biomarker performance for the detection of hepatocellular carcinoma by inclusion of clinical parameters

机译:通过包括临床参数,改善了用于检测肝细胞癌的生物标志物性能

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We have previously identified several biomarkers of hepatocellular carcinoma (HCC). The levels of three of these biomarkers were analyzed individually and in combination with the currently used marker, alpha fetoprotein (AFP), for the ability to distinguish between a diagnosis of cirrhosis (n=113) and HCC (n=164). We have utilized several novel biostatistical tools, along with the inclusion of clinical factors such as age and gender, to determine if improved algorithms could be used to increase the probability of detection of cancer. Using several of these methods, we are able to detect HCC in the background of cirrhosis with an AUC of at least 0.95. The use of clinical factors in combination with biomarker values to detect HCC is discussed.
机译:我们先前已经确定了肝细胞癌(HCC)的几种生物标志物。单独分析了三种生物标志物的水平,并与当前使用的标志物甲胎蛋白(AFP)进行了分析,以区分肝硬化诊断(n = 113)和肝癌(n = 164)。我们利用了几种新颖的生物统计工具,并结合了诸如年龄和性别之类的临床因素,以确定是否可以使用改进的算法来增加检测癌症的可能性。使用这些方法中的几种,我们能够以至少0.95的AUC检测到肝硬化背景中的HCC。讨论了将临床因素与生物标志物值结合使用以检测HCC。

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