Tilki Derya, Kim Sun Il, Hu Brian, Dall'Era Marc A, Evans Christopher P
Martini-Clinic Prostate Cancer Center and Department of Urology, University Hospital Hamburg-Eppendorf, Hamburg, Germany; Department of Urology, School of Medicine, University of California-Davis, Sacramento, California.
Department of Urology, School of Medicine, University of California-Davis, Sacramento, California; Department of Urology, Ajou University School of Medicine, Suwon, Republic of Korea.
J Urol. 2015 May;193(5):1525-31. doi: 10.1016/j.juro.2014.10.087. Epub 2014 Oct 22.
Prostate specific antigen is an important tool to monitor patients with prostate cancer after radical prostatectomy. Ultrasensitive prostate specific antigen assays are increasingly used with a lower limit of detection as low as 0.001 ng/ml. We systematically reviewed currently available ultrasensitive prostate specific antigen technologies and the role of this method in monitoring patients after radical prostatectomy.
We searched the relevant literature using the MEDLINE® database. For various study objectives the series eligible for review provided serial ultrasensitive prostate specific antigen (lower detection limit less than 0.1 ng/ml) data on men after radical prostatectomy as well as comparative data on standard prostate specific antigen (lower detection limit 0.1 ng/ml or greater).
Ultrasensitive prostate specific antigen could potentially detect prostate cancer recurrence years earlier than standard prostate specific antigen assays. The specificity of detectable ultrasensitive prostate specific antigen is low. Ultrasensitive prostate specific antigen kinetics may improve the positive predictive value for detecting cancer recurrence. However, the usefulness of prostate specific antigen doubling time at the ultrasensitive level remains controversial. Undetectable nadir ultrasensitive prostate specific antigen after radical prostatectomy confers a low risk of disease recurrence while a detectable nadir above 0.01 ng/ml requires additional measurement and consideration of other risk factors to determine management and avoid overtreatment. This monitoring method may spare patients with high risk disease adjuvant radiation therapy and enable more selective early salvage radiation. Currently no data demonstrate improved survival after early salvage therapy prompted by ultrasensitive prostate specific antigen surveillance.
Ultrasensitive prostate specific antigen is useful in the early diagnosis of cancer recurrence after radical prostatectomy but specificity is poor. To date there is a lack of evidence that earlier detection of recurrence translates into prolonged time to metastasis. Integrating ultrasensitive prostate specific antigen with other clinicopathological factors can help determine optimal adjuvant and salvage therapy.
前列腺特异性抗原是根治性前列腺切除术后监测前列腺癌患者的重要工具。超敏前列腺特异性抗原检测方法的使用越来越多,检测下限低至0.001 ng/ml。我们系统回顾了目前可用的超敏前列腺特异性抗原技术以及该方法在根治性前列腺切除术后监测患者中的作用。
我们使用MEDLINE®数据库检索相关文献。对于各种研究目标,符合综述条件的系列研究提供了根治性前列腺切除术后男性的系列超敏前列腺特异性抗原(检测下限小于0.1 ng/ml)数据以及标准前列腺特异性抗原(检测下限为0.1 ng/ml或更高)的比较数据。
超敏前列腺特异性抗原可能比标准前列腺特异性抗原检测早数年发现前列腺癌复发。可检测到的超敏前列腺特异性抗原的特异性较低。超敏前列腺特异性抗原动力学可能会提高检测癌症复发的阳性预测值。然而,超敏水平下前列腺特异性抗原倍增时间的实用性仍存在争议。根治性前列腺切除术后无法检测到的最低超敏前列腺特异性抗原表明疾病复发风险较低,而可检测到的最低值高于0.01 ng/ml则需要进一步测量并考虑其他风险因素以确定治疗方案并避免过度治疗。这种监测方法可能使高危疾病患者免于辅助放疗,并实现更具选择性的早期挽救性放疗。目前尚无数据表明超敏前列腺特异性抗原监测促使的早期挽救性治疗能提高生存率。
超敏前列腺特异性抗原在根治性前列腺切除术后癌症复发的早期诊断中有用,但特异性较差。迄今为止,缺乏证据表明早期发现复发能转化为延长至转移的时间。将超敏前列腺特异性抗原与其他临床病理因素相结合有助于确定最佳的辅助和挽救性治疗方案。