Pelzer Alexandre E, Bektic Jasmin, Akkad Thomas, Ongarello Stefano, Schaefer Georg, Schwentner Christian, Frauscher Ferdinand, Bartsch Georg, Horninger Wolfgang
Department of Urology, Medical University Innsbruck and Institute of Analytical Chemistry and Radiochemistry, Innsbruck, Austria.
J Urol. 2007 Jul;178(1):93-7; discussion 97. doi: 10.1016/j.juro.2007.03.021. Epub 2007 May 11.
Since the implementation of widespread serum total prostate specific antigen based screening, the risk of prostate cancer over diagnosis has become a concern. We evaluated the amount of possible over and under diagnosis of prostate cancer in an asymptomatic screening population with a total prostate specific antigen of 2.0 to 3.9 (lower range) and 4.0 to 10.0 ng/ml (higher range).
A total of 680 patients with prostate cancer were included. Possible over diagnosis was defined as Gleason score less than 7, pathological stage pT2a and negative surgical margins. Under diagnosis was defined as pathological stage pT3 or greater, or positive surgical margins. Furthermore, insignificant tumors according to the Epstein criteria were evaluated in a small subset of patients for whom cancer volume information was available.
In the lower and higher total prostate specific antigen ranges there was an over diagnosis rate of 19.7% and 16.5%, and an under diagnosis rate of 18.9%* and 36.7%, respectively (p<0.05). In the prostate specific antigen range of 2.0 to 10.0 ng/ml combined the rates of over and under diagnosis were 17.6% and 30.3%, respectively. In addition, 8.7% of tumors with total prostate specific antigen 2.0 to 10.0 ng/ml met the Epstein criteria for insignificance.
These data show that the reported estimates of over diagnosis in the low total prostate specific antigen group are exaggerated in a screening population. Using our criteria prostate cancer under diagnosis occurs more frequently than over diagnosis in the total prostate specific antigen range of 4.0 to 10 ng/ml.
自从广泛开展基于血清总前列腺特异性抗原的筛查以来,前列腺癌过度诊断的风险已成为一个关注点。我们评估了在无症状筛查人群中,总前列腺特异性抗原为2.0至3.9(较低范围)和4.0至10.0 ng/ml(较高范围)时前列腺癌可能的过度诊断和漏诊情况。
共纳入680例前列腺癌患者。可能的过度诊断定义为Gleason评分小于7、病理分期pT2a且手术切缘阴性。漏诊定义为病理分期pT3或更高,或手术切缘阳性。此外,根据爱泼斯坦标准,对一小部分可获得癌体积信息的患者中的微小肿瘤进行了评估。
在较低和较高的总前列腺特异性抗原范围内,过度诊断率分别为19.7%和16.5%,漏诊率分别为18.9%*和36.7%(p<0.05)。在2.0至10.0 ng/ml的总前列腺特异性抗原范围内,过度诊断率和漏诊率分别为17.6%和30.3%。此外,总前列腺特异性抗原为2.0至10.0 ng/ml的肿瘤中有8.7%符合爱泼斯坦微小肿瘤标准。
这些数据表明,在筛查人群中,低总前列腺特异性抗原组中报道的过度诊断估计值被夸大了。根据我们的标准,在总前列腺癌在总前列腺特异性抗原为4.0至10 ng/ml的范围内,漏诊比过度诊断更常见。