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Prognostic significance of high-grade prostatic intraepithelial neoplasia (HGPIN): risk of prostatic cancer on repeat biopsies.

机译:高度前列腺上皮内瘤变(HGPIN)的预后意义:重复活检时有前列腺癌的风险。

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OBJECTIVES: To verify prognostic significance of high-grade prostatic intraepithelial neoplasia (HGPIN) in 65 patients who underwent repeat biopsies with a mean follow-up of 36 months. METHODS: In June 2007, after a retrospective revision of the biopsy reports that were performed between January 2002 and December 2006 because of prostate specific antigen (PSA) values greater than 4 ng/mL, but no clinical or ultrasonographic parameters indicative of prostatic cancer (CaP), we selected 65 patients (group 1) (mean age 63.4 years) with initial HGPIN diagnosis and a control group of another 65 patients (group 2) (mean age 64.5 years) with initial diagnosis of benign prostatic tissue (BPT). All the patients underwent rebiopsies 3 to 12, 13 to 24, 25 to 36, and 37 to 48 months after biopsy. After each rebiopsy, 3 diagnoses were made: BPT, HGPIN, and CaP. Prognostic significance of PSA and HGPIN focality at biopsy were also assessed. RESULTS: Overall, CaP was detected in 14 of 65 (21.5%) group 1 patients and in 15 of 65 (23.0%) group 2 patients. No significant difference was reported between the 2 groups in terms of risk for CaP. Low-medium risk cancer was reported in 12 of 14 (85.7%) cases in group 1 and in 12 of 15 (80.0%) of group 2, mainly after the second rebiopsy. PSA and HGPIN focality at biopsy did not seem to predict CaP diagnosis. CONCLUSIONS: The risk for cancer after HGPIN diagnosis (21.5%) was not higher than the risk reported after BPT diagnosis (23.0%). PSA and HGPIN focality at biopsy do not enhance cancer predictivity. Patients with a HGPIN diagnosis do not seem to need any different follow-up rebiopsy strategy than patients with a BPT diagnosis.
机译:目的:验证65例接受重复活检并平均随访36个月的患者的高级别前列腺上皮内瘤变(HGPIN)的预后意义。方法:回顾性修订2002年1月至2006年12月间进行的活检报告,原因是前列腺特异性抗原(PSA)值大于4 ng / mL,但没有临床或超声检查指标提示前列腺癌( CaP),我们选择了65例初发HGPIN诊断的患者(第1组)(平均年龄63.4岁)和对照组,另外65例初诊为良性前列腺组织(BPT)的患者(第2组)(平均年龄64.5岁)。所有患者均在活检后3至12、13至24、25至36和37至48个月进行了活检。每次活检后,进行3次诊断:BPT,HGPIN和CaP。还评估了PSA和HGPIN病灶在活检中的预后意义。结果:总体而言,在65例(21.5%)的第1组患者中检测到CaP,在65例(23.0%)的第2组患者中检测到CaP。就发生CaP的风险而言,两组之间均无明显差异。第1组14例中的12例(85.7%)和2组15例中的12例(80.0%)报告了低中度癌症,主要是在第二次活检后。 PSA和HGPIN活检的局灶性似乎不能预测CaP的诊断。结论HGPIN诊断后患癌症的风险(21.5%)不高于BPT诊断后报告的癌症的风险(23.0%)。活检的PSA和HGPIN聚焦不能增强癌症的可预测性。 HGPIN诊断的患者与BPT诊断的患者似乎不需要任何不同的随访活检策略。

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