首页> 外文期刊>The Journal of Urology >Lifelong yearly prostate specific antigen surveillance is not necessary for low risk prostate cancer treated with radical prostatectomy.
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Lifelong yearly prostate specific antigen surveillance is not necessary for low risk prostate cancer treated with radical prostatectomy.

机译:对于经根治性前列腺切除术治疗的低危前列腺癌,终身进行年度前列腺特异性抗原监测是不必要的。

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PURPOSE: Many patients undergoing radical prostatectomy in the prostate specific antigen era have a low risk of recurrence. Aggressive postoperative prostate specific antigen surveillance is costly and anxiety provoking. In this study we investigate the need for yearly prostate specific antigen measurements in patients with surgically treated low risk prostate cancer. MATERIALS AND METHODS: We identified 2,219 patients who underwent radical prostatectomy between 1994 and 2004 for low risk localized prostate cancer. Low risk was defined as prostate specific antigen less than 10 ng/ml, pathological stage pT2c or less, Gleason score 6 or less, negative lymph nodes and negative surgical margins. Patients who underwent neoadjuvant or adjuvant therapy were excluded from analysis. Biochemical failure was defined as a prostate specific antigen greater than 0.4 ng/ml and prostate specific antigen values less than 0.15 ng/ml were considered undetectable. Biochemical failure rates were calculated according to the duration of the prostate specific antigen-free period after radical prostatectomy. RESULTS: A total of 142 (6.4%) patients experienced biochemical failure during the course of the study. The risk of biochemical failure decreased with increasing duration of the prostate specific antigen-free interval. For example 1, 3 and 5-year biochemical failure rates calculated at surgery were 1.8%, 4.2% and 6.3%, respectively. For patients with undetectable prostate specific antigen measurements 5 years after surgery the 1, 3 and 5-year biochemical failure rates were 0.0%, 0.7% and 1.3%, respectively. In addition, 1-year biochemical failure rates were 0.2%, 0.4%, 0.0% and 0.0% after a prostate specific antigen-free period of 1, 3, 5 and 10 years, respectively. CONCLUSIONS: The risk of biochemical failure is inversely proportional to the duration of the prostate specific antigen-free interval after radical prostatectomy in low risk patients. Biochemical failure 1 year after an undetectable prostate specific antigen is uncommon, especially after a prostate specific antigen-free period of 3 years. These data suggest that annual prostate specific antigen measurements are unnecessary, especially after a prostate specific antigen-free interval of 3 years. Prostate specific antigen measurements every 2 years should capture the majority of low risk patients who experience progression.
机译:目的:许多在前列腺特异性抗原时代接受根治性前列腺切除术的患者复发的风险较低。积极的术后前列腺特异抗原监测成本高昂,并且令人不安。在这项研究中,我们调查了接受手术治疗的低危前列腺癌患者每年需要进行前列腺特异性抗原测量的情况。材料与方法:我们确定了1994年至2004年之间因低风险局限性前列腺癌接受过前列腺癌根治术的2,219例患者。低风险定义为前列腺特异性抗原低于10 ng / ml,病理分期pT2c或更低,格里森评分6或更低,淋巴结阴性和手术切缘阴性。分析排除了接受新辅助或辅助治疗的患者。生化衰竭定义为大于0.4 ng / ml的前列腺特异性抗原,小于0.15 ng / ml的前列腺特异性抗原值被认为不可检测。根据根治性前列腺切除术后前列腺特异性无抗原期的持续时间计算生化失败率。结果:在研究过程中,共有142名患者(6.4%)经历了生化衰竭。随着前列腺特异性无抗原间隔时间的延长,生化失败的风险降低。例如,在手术中计算出的1年,3年和5年生化失败率分别为1.8%,4.2%和6.3%。对于术后5年无法检测到前列腺特异性抗原的患者,其1、3和5年生化失败率分别为0.0%,0.7%和1.3%。另外,在1、3、5和10年的前列腺特异性无抗原期后,一年生化失败率分别为0.2%,0.4%,0.0%和0.0%。结论:低危患者根治性前列腺切除术后生化失败的风险与前列腺特异性无抗原间隔的持续时间成反比。不可检测到的前列腺特异抗原后1年的生化衰竭罕见,尤其是在3年无前列腺特异抗原的时期后。这些数据表明,不需要每年进行前列腺特异性抗原测量,尤其是在3年无前列腺特异性抗原间隔之后。每2年进行一次前列腺特异性抗原测量,应可捕获大多数经历进展的低风险患者。

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