Erasmus MC, University Medical Centre, Department of Urology, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.
Eur Urol. 2010 Oct;58(4):475-81. doi: 10.1016/j.eururo.2010.06.039. Epub 2010 Jul 9.
The performance characteristics of serum prostate-specific antigen (PSA) as a diagnostic test for prostate cancer (PCa) are poor. The performance of the PCa antigen 3 (PCA3) gene as a primary diagnostic is unknown.
Assess the value of PCA3 as a first-line diagnostic test.
DESIGN, SETTING AND PARTICIPANTS: Participants included men aged 63-75 who were invited for rescreening in the period from September 2007 to February 2009 within the European Randomised Study of Screening for Prostate Cancer, Rotterdam section.
Lateral sextant biopsies were performed if the serum PSA value was > or =3.0 ng/ml and/or the PCA3 score was > or =10.
Measurements included distribution and correlation of PSA value and PCA3 score and their relation to the number of cases and the characteristics of PCa detected. Additional value of PCA3 was included in men with previous negative biopsy and/or PSA <3.0 ng/ml.
In 721 men, all biopsied, 122 PCa cases (16.9%) were detected. Correlation between PSA and PCA3 is poor (Spearman rank correlation: ρ=0.14; p<0.0001). A PSA > or =3.0 ng/ml misses 64.7% of the total PCa that can be detected with the sextant biopsy technique and 57.9% of serious PCa (T2a or higher and/or Gleason grade > or =4, n=19), and 68.2% of biopsies could have been avoided; the respective data for PCA3 > or =35 are 32%, 26.3%, and 51.7%. Performance of PCA3 in men with low PSA (area under the curve [AUC]: 0.63) and/or previous negative biopsy (AUC: 0.68) is unclear but has limited reliability due to small numbers.
PCA3 as a first-line screening test shows improvement of the performance characteristics and identification of serious disease compared with PSA in this prescreened population.
血清前列腺特异性抗原(PSA)作为前列腺癌(PCa)诊断检测的性能特征较差。前列腺癌抗原 3(PCA3)基因作为主要诊断方法的性能尚不清楚。
评估 PCA3 作为一线诊断检测的价值。
设计、地点和参与者:参与者包括年龄在 63-75 岁之间的男性,他们于 2007 年 9 月至 2009 年 2 月期间在荷兰鹿特丹欧洲前列腺癌筛查随机研究的重新筛查期间被邀请参加。
如果血清 PSA 值> =3.0ng/ml 和/或 PCA3 评分> =10,则进行侧方六区活检。
测量包括 PSA 值和 PCA3 评分的分布和相关性,以及它们与病例数和检测到的 PCa 特征的关系。在之前活检阴性和/或 PSA<3.0ng/ml 的男性中,包括 PCA3 的附加价值。
在 721 名接受活检的男性中,共检测到 122 例 PCa 病例(16.9%)。PSA 与 PCA3 之间的相关性较差(Spearman 等级相关系数:ρ=0.14;p<0.0001)。PSA> =3.0ng/ml 会错过六区活检技术可检测到的总 PCa 的 64.7%和严重 PCa(T2a 或更高和/或 Gleason 分级> =4,n=19)的 57.9%,可避免 68.2%的活检;相应的 PCA3> =35 的数据分别为 32%、26.3%和 51.7%。在 PSA 较低(曲线下面积[AUC]:0.63)和/或之前活检阴性的男性中,PCA3 的性能(AUC:0.68)尚不清楚,但由于数量较少,可靠性有限。
在这个预筛查人群中,与 PSA 相比,PCA3 作为一线筛查检测可改善性能特征并识别严重疾病。