首页> 外文期刊>Urology >Evaluation of prostAsure index in the detection of prostate cancer: a preliminary report (see comments)
【24h】

Evaluation of prostAsure index in the detection of prostate cancer: a preliminary report (see comments)

机译:在前列腺癌的检测中评估prostAsure指数:初步报告(请参阅评论)

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVES: Although prostate-specific antigen (PSA) has revolutionized the detection of prostate cancer, it has definite limitations with respect to its clinical sensitivity and specificity. Because a substantial number (20% to 40%) of men undergoing radical prostatectomy have a PSA level of 4.0 ng/mL or less, any new test offering diagnostic improvement must perform well in patients whose PSA level is less than or equal to 4.0 ng/mL, as well as in patients whose PSA is greater than 4.0 ng/mL. The performances of two tests, the ProstAsure index and the percent free PSA test, were evaluated in detecting cancer. METHODS: We retrospectively analyzed serum samples from 225 men who were grouped into three categories: 94 men who had a normal digital rectal examination and a serum PSA level of 4.0 ng/mL or less, 77 men who were clinically suspected of having benign prostatic hyperplasia (BPH) with a serum PSA level of 4.0 ng/mL or less, and 54 men with localized prostate cancer. The PSA assays were performed using the Hybritech and Tosoh assays and the ProstAsure index was determined by Global Health Net, Savannah, Ga. Receiver operator characteristic (ROC) curves were constructed to evaluate the performance of these two tests, and the areas under the curve were compared for significance. RESULTS: The sensitivity and specificity of detecting prostate cancer using ProstAsure were 93% and 81%, respectively. Using a cutoff value of 15%, the sensitivity and specificity of detecting cancer for percent free PSA were 80% and 74%, respectively (sensitivity increased to 93% and specificity to 59% for free PSA at 19%). In men with a total serum PSA level of 4.0 ng/mL or less, ProstAsure had a lower false-positive rate compared to free PSA level at 19% for men with or without clinical BPH as well as for men without clinical BPH using a 15% free PSA threshold. ProstAsure left fewer cancers undetected (7%) compared to free PSA at the 15% cutoff (20%). CONCLUSIONS: In this study of selected men, ROC curve analysis shows a statistically significant advantage in performance (P = 0.0023) for the ProstAsure index compared to free PSA in detecting prostate cancer.
机译:目的:尽管前列腺特异性抗原(PSA)彻底改变了前列腺癌的检测方法,但在临床敏感性和特异性方面仍存在一定局限性。由于接受前列腺癌根治术的男性中有很大一部分(20%至40%)的PSA水平为4.0 ng / mL或更低,因此任何新的能够提供诊断性改善的测试都必须在PSA水平小于或等于4.0 ng的患者中表现良好/ mL,以及PSA大于4.0 ng / mL的患者。在检测癌症中评估了两种测试的性能,即ProstAsure指数和游离PSA百分比测试。方法:我们回顾性分析了来自225名男性的血清样本,这些样本被分为三类:94例直肠指检正常且血清PSA水平为4.0 ng / mL或以下,77例临床怀疑为前列腺增生的男性(BPH)的血清PSA水平为4.0 ng / mL或更低,并且有54名男性患有局限性前列腺癌。使用Hybritech和Tosoh测定进行PSA测定,ProstAsure指数由乔治亚州萨凡纳市的Global Health Net确定。构建接收者操作员特征(ROC)曲线以评估这两项测试的性能以及曲线下的面积比较重要性。结果:使用ProstAsure检测前列腺癌的敏感性和特异性分别为93%和81%。使用15%的临界值,检测到的癌症对于游离PSA百分比的敏感性和特异性分别为80%和74%(对于游离PSA为19%的敏感性,敏感性提高到93%,特异性达到59%)。对于总血清PSA水平为4.0 ng / mL或更低的男性,有或没有临床BPH的男性和没有临床BPH的男性使用15的男性,ProstAsure的假阳性率均低于游离PSA的19%。免费PSA阈值百分比。与15%截止(20%)的免费PSA相比,ProstAsure留下更少的未被发现的癌症(7%)。结论:在这项针对选定男性的研究中,ROC曲线分析显示,与游离PSA相比,ProstAsure指数在检测前列腺癌方面的表现具有统计学上的显着优势(P = 0.0023)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号