Division of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network and University of Toronto, Toronto, Ontario, Canada.
Division of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network and University of Toronto, Toronto, Ontario, Canada.
J Urol. 2018 Nov;200(5):1056-1061. doi: 10.1016/j.juro.2018.05.017. Epub 2018 Jul 27.
Longitudinal cohort studies and guidelines demonstrate that prostate specific antigen 1 ng/ml or greater in younger patients confers an increased risk of delayed prostate cancer death. At our institution we have used an aggressive biopsy strategy in younger patients with prostate specific antigen 1 ng/ml or greater. Our objective was to determine the proportion of detected cancer and specifically clinically significant cancer by this strategy.
The prostate biopsy database at Princess Margaret Cancer Centre was queried for patients younger than 50 years who underwent a first prostate biopsy between 2000 and 2016. We included only patients who underwent prostate biopsy due to prostate specific antigen 1 ng/ml or greater and those with a suspicious digital rectal examination, a positive family history or a suspicious lesion on transrectal ultrasound. All clinical and pathological parameters were analyzed. Patients were stratified according to specific prostate specific antigen values. Multivariable logistic regression was performed to ascertain predictors of any prostate cancer diagnosis and of clinically significant prostate cancer.
Of the 199 patients who met study inclusion criteria 37 (19%) were diagnosed with prostate cancer and 8 (22%) had a Gleason score of 7 or greater. Of those diagnosed with prostate cancer 25 (68%) had prostate specific antigen 1.5 ng/ml or greater and all men with a Gleason score of 7 or greater had prostate specific antigen 1.5 ng/ml or greater. Notably 19 patients (51%) had prostate cancer exceeding the Epstein criteria for active surveillance. Factors predicting prostate cancer included a positive family history, rising prostate specific antigen and lower prostate volume.
Our results justify adopting an aggressive prostate biopsy strategy in men younger than 50 years with prostate specific antigen 1.5 ng/ml or greater while patients with prostate specific antigen less than 1.5 ng/ml are unlikely to have significant cancer. Special attention should be given to patients with a smaller prostate and a positive family history.
纵向队列研究和指南表明,年轻患者前列腺特异性抗原(PSA)水平为 1ng/ml 或更高与前列腺癌死亡风险增加相关。在我们的机构中,我们对 PSA 水平为 1ng/ml 或更高的年轻患者采用了积极的活检策略。我们的目的是确定该策略检测到的癌症,特别是临床显著癌症的比例。
在玛格丽特公主癌症中心的前列腺活检数据库中,对 2000 年至 2016 年间接受首次前列腺活检的年龄小于 50 岁的患者进行了查询。我们仅包括因 PSA 水平为 1ng/ml 或更高而接受前列腺活检的患者,以及那些直肠指检可疑、家族史阳性或经直肠超声检查发现可疑病灶的患者。分析所有临床和病理参数。根据特定的 PSA 值对患者进行分层。采用多变量逻辑回归确定任何前列腺癌诊断和临床显著前列腺癌的预测因素。
在符合研究纳入标准的 199 名患者中,37 名(19%)诊断为前列腺癌,8 名(22%)前列腺癌分级为 7 级或更高。在诊断为前列腺癌的患者中,25 名(68%)PSA 水平为 1.5ng/ml 或更高,所有前列腺癌分级为 7 级或更高的患者 PSA 水平均为 1.5ng/ml 或更高。值得注意的是,19 名患者(51%)的前列腺癌超过了主动监测的 Epstein 标准。预测前列腺癌的因素包括家族史阳性、PSA 升高和前列腺体积减小。
我们的结果证明,对于 PSA 水平为 1.5ng/ml 或更高的年龄小于 50 岁的男性,应采用积极的前列腺活检策略,而 PSA 水平低于 1.5ng/ml 的患者不太可能患有显著的癌症。应特别关注前列腺较小和家族史阳性的患者。