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[用于前列腺癌检测的新生物标志物及多变量模型的应用]

[New biomarkers and application of multivariate models for detection of prostate cancer].

作者信息

Stephan C, Cammann H, Rittenhouse H, Lein M, Jentzmik F, Schrader M, Deger S, Miller K, Jung K

机构信息

Klinik für Urologie, Charité - Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Aktuelle Urol. 2009 Aug;40(4):221-30. doi: 10.1055/s-0029-1224535. Epub 2009 Jul 24.

Abstract

The specificity of PSA has been enhanced by using molecular forms of PSA and free PSA (fPSA) such as percent free PSA (%fPSA), proPSA, intact PSA or BPHA and / or new serum markers. Most of these promising new serum markers like EPCA2 or ANXA3 still lack confirmation of the outstanding initial results or show only marginally enhanced specificity at high sensitivity levels. PCA3, TMPRSS2-ERG, and other analytes in urine collected after digital rectal examination with application of mild digital pressure have the potential to preferentially detect aggressive PCa and to decrease the number of unnecessary repeat biopsies. The combination of these new urinary markers with new and established serum markers seems to be most promising to further increase specificity of tPSA. Multivariate models, e. g., artificial neural networks (ANN) or logistic regression (LR) based nomograms have recently been performed by incorporating these new markers in several studies. There is generally an advantage to include the new markers and clinical data as additional parameters to PSA and %fPSA within ANN and LR models. Results of these studies and also unexpected pitfalls are discussed in this review.

摘要

通过使用前列腺特异性抗原(PSA)的分子形式和游离PSA(fPSA),如游离PSA百分比(%fPSA)、前PSA、完整PSA或BPHA和/或新的血清标志物,PSA的特异性得到了提高。大多数这些有前景的新血清标志物,如EPCA2或ANXA3,仍缺乏对出色初始结果的确认,或在高灵敏度水平下仅显示出略微提高的特异性。前列腺癌抗原3(PCA3)、跨膜丝氨酸蛋白酶2-ETS相关基因(TMPRSS2-ERG)以及在指诊后施加轻度指压收集的尿液中的其他分析物,有可能优先检测侵袭性前列腺癌,并减少不必要的重复活检次数。这些新的尿液标志物与新的和已确立的血清标志物相结合,似乎最有希望进一步提高总PSA(tPSA)的特异性。最近,在几项研究中通过纳入这些新标志物进行了多变量模型,例如基于人工神经网络(ANN)或逻辑回归(LR)的列线图。在ANN和LR模型中,将新标志物和临床数据作为PSA和%fPSA的附加参数通常具有优势。本综述讨论了这些研究的结果以及意外的陷阱。

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