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Optimal Monitoring of Prostate-Specific Antigen Detects Prostate Cancer at the Localized Stage after Photoselective Vaporization for Benign Prostatic Hyperplasia

机译:前列腺特异性抗原的最佳监测在良性前列腺增生的光学蒸发后检测局部阶段的前列腺癌

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Introduction: Photoselective vaporization of the prostate (PVP) does not provide prostate tissue for pathologic analysis. Here, we carried out early monitoring for prostate cancer by measuring prostate-specific antigen (PSA) levels and assessing clinicopathological features after PVP. Materials and Methods: Patients (n = 800) who underwent PVP and were followed-up for more than 12 months were analyzed retrospectively. After PVP, PSA levels were measured at 3 and 12 months and each year thereafter. Prostate biopsies were performed when PSA levels increased continuously. We assessed the characteristics of patients diagnosed with prostate cancer. Results: The mean follow-up period was 49 months. After PVP, 54 patients underwent biopsies, and 23 patients were diagnosed with prostate cancer. Overall, 10, 10, and 3 patients had clinical stage T1c, T2a, and T2b disease, respectively, and there were no cases of stage T2c disease or greater. Conclusions: We found that it was possible to diagnose prostate cancer at a localized stage under our optimal PSA monitoring schedule before and after PVP.
机译:介绍:前列腺(PVP)的光电蒸发不提供用于病理分析的前列腺组织。在这里,我们通过测量前列腺特异性抗原(PSA)水平并评估PVP后评估临床病理特征进行前列腺癌进行早期监测。材料和方法:回顾性地分析了PVP和随访超过12个月的患者(n = 800)。 PVP后,PSA水平在3和12个月内测量,此后每年测量。当PSA水平连续增加时,进行前列腺活组织检查。我们评估了被诊断患有前列腺癌的患者的特征。结果:平均随访期为49个月。 PVP后,54名患者接受活检,23例患者被诊断出癌症。总体而言,10,10和3名患者分别具有临床阶段T1C,T2A和T2B疾病,并且没有阶段T2C病或更大的情况。结论:我们发现在PVP之前和之后的最佳PSA监测计划下,可以在本地化阶段诊断前列腺癌。

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