Schostak Martin, Schwall Gerhard P, Poznanović Slobodan, Groebe Karlfried, Müller Markus, Messinger Diethelm, Miller Kurt, Krause Hans, Pelzer Alexandre, Horninger Wolfgang, Klocker Helmut, Hennenlotter Jörg, Feyerabend Susan, Stenzl Arnulf, Schrattenholz André
Department of Urology, Charité University Medicine in Berlin, Campus Benjamin Franklin, Berlin, Berlin, Germany.
J Urol. 2009 Jan;181(1):343-53. doi: 10.1016/j.juro.2008.08.119. Epub 2008 Nov 13.
In prostate cancer cases the early diagnosis of tumors carrying a high risk of progression is of the utmost importance. There is an urgent clinical need to avoid unnecessary biopsies and subsequent overtreatment. We validated annexin A3 as a diagnostic marker for prostatic disease in typical clinical populations and relevant segments, such as patients with a negative digital rectal examination and low prostate specific antigen.
We performed a blinded clinical study (ClinicalTrials.gov Identifier NCT00400894) from September 2005 to January 2007 in 591 patients who were continuously recruited from 4 European urological clinics. Urine was obtained directly after digital rectal examination and the annexin A3 concentration in urine was quantified by Western blot. Statistical analysis included combinations of annexin A3 with total, percent free, complexed and percent complexed prostate specific antigen.
Combined readouts of prostate specific antigen and urinary annexin A3 were superior to all others with an area under the ROC curve of 0.82 for a total prostate specific antigen range of 2 to 6 ng/ml, 0.83 for a total prostate specific antigen range of 4 to 10 ng/ml and 0.81 in all patients. The best performing prostate specific antigen derivative was percent free prostate specific antigen with an area under the ROC curve of 0.68 for a total prostate specific antigen range of 2 to 6 ng/ml, 0.72 for a total prostate specific antigen range of 4 to 10 ng/ml and 0.73 in all patients. Annexin A3 has an inverse relationship to cancer and, therefore, its specificity was much better than that of prostate specific antigen.
Annexin A3 quantification in urine provides a novel noninvasive biomarker with high specificity. Annexin A3 is complementary to prostate specific antigen or to any other cancer marker. It has a huge potential to avoid unnecessary biopsies with a particular strength in the clinically relevant large group of patients who have a negative digital rectal examination and prostate specific antigen in the lower range of values (2 to 10 ng/ml).
在前列腺癌病例中,对具有高进展风险的肿瘤进行早期诊断至关重要。临床上迫切需要避免不必要的活检及后续的过度治疗。我们在典型临床人群及相关亚组中,如直肠指检阴性且前列腺特异性抗原水平较低的患者中,验证了膜联蛋白A3作为前列腺疾病诊断标志物的有效性。
2005年9月至2007年1月,我们在来自4家欧洲泌尿外科诊所连续招募的591例患者中开展了一项盲法临床研究(ClinicalTrials.gov标识符:NCT00400894)。直肠指检后直接采集尿液,采用蛋白质印迹法对尿液中膜联蛋白A3的浓度进行定量分析。统计分析包括膜联蛋白A3与总前列腺特异性抗原、游离前列腺特异性抗原百分比、复合前列腺特异性抗原以及复合前列腺特异性抗原百分比的联合分析。
对于总前列腺特异性抗原范围为2至6 ng/ml的情况,前列腺特异性抗原与尿膜联蛋白A3的联合检测结果优于其他所有检测,ROC曲线下面积为0.82;对于总前列腺特异性抗原范围为4至10 ng/ml的情况,ROC曲线下面积为0.83;在所有患者中,ROC曲线下面积为0.81。表现最佳的前列腺特异性抗原衍生物是游离前列腺特异性抗原百分比,对于总前列腺特异性抗原范围为2至6 ng/ml的情况,ROC曲线下面积为0.68;对于总前列腺特异性抗原范围为4至10 ng/ml的情况,ROC曲线下面积为0.72;在所有患者中,ROC曲线下面积为0.73。膜联蛋白A3与癌症呈负相关,因此其特异性远优于前列腺特异性抗原。
尿液中膜联蛋白A3的定量分析提供了一种具有高特异性的新型非侵入性生物标志物。膜联蛋白A3可作为前列腺特异性抗原或任何其他癌症标志物的补充。它在避免不必要活检方面具有巨大潜力,对于直肠指检阴性且前列腺特异性抗原处于较低值范围(2至10 ng/ml)的临床相关大群体患者尤为有效。