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Pathological Patterns of Prostate Biopsy in Men with Fluctuations of Prostate Cancer Gene 3 Score: A Preliminary Report

机译:前列腺癌基因3评分波动的男性前列腺穿刺活检的病理模式:初步报告

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Background: To evaluate pathological patterns of prostate biopsy in men with changes in risk class by prostate cancer gene 3 (PCA3) score and with elevated serum prostate-specific antigen (PSA) or positive digital rectal examination (DRE), undergoing a repeat biopsy. Patients and Methods: A total of 108 males of two Italian Institutions who had undergone at least two PCA3 score assessments with changed PCA3 risk class were selected. Comparison of PCA3 score in patients with negative re-biopsy [normal parenchyma, benign prostatic hyperplasia (BPH), chronic prostatitis, high-grade prostate intraepithelial neoplasia (HG-PIN), atypical small acinar prostate (ASAP)] or positive re-biopsy was performed. Results: The up-and down-grading rates for PCA3 score were 71.3% (n=77) and 28.7% (n=31), respectively. Among the 77 up-graded patients, the median change in PCA3 score was 24 (range=4-69), while among the 31 down-graded ones, the median change was 17 (2 to 55). The PCA3 score in 24 out of 29 (82.7%) patients with prostate cancer (PCa) was up-graded. No association was found for correlation of PCA3 score change with age >65 years (p=0.975), family history of prostate cancer (p=0.796), positive DRE (p=0.179), use of 5-alpha-reductase inhibitors (p=0.793) and BPH/prostatitis/HG-PIN/ASAP diagnosis (p=0.428). Conclusion: PCA3 score can be considered a marker that is stable over time in most cases; notably, up to 20% of patients have a clinically relevant change of risk class. The rate of PCa was higher in patients whose PCA3 score was up-graded, even if no robust cut-off for PCA3 score fluctuation was identified.
机译:背景:通过前列腺癌基因3(PCA3)评分,高血清前列腺特异性抗原(PSA)或阳性直肠指检(DRE)进行重复活检,评估男性的前列腺活检的病理学类型,其风险类别发生变化。患者和方法:选择两所意大利机构的108名男性,他们接受了至少两次PCA3评分评估,并且PCA3风险等级发生了变化。再活检阴性[正常实质,良性前列腺增生(BPH),慢性前列腺炎,高级别前列腺上皮内瘤变(HG-PIN),非典型小腺泡前列腺癌(ASAP)]或再活检阳性的患者PCA3评分的比较被执行了。结果:PCA3评分的上,下评级率分别为71.3%(n = 77)和28.7%(n = 31)。在77例升级患者中,PCA3评分的中位数变化为24(范围= 4-69),而在31例降级患者中,PCA3评分的中位数变化为17(2至55)。在29名(82.7%)前列腺癌(PCa)患者中,有24位的PCA3评分被提升。未发现PCA3评分变化与年龄> 65岁(p = 0.975),前列腺癌家族史(p = 0.796),DRE阳性(p = 0.179),使用5-α-还原酶抑制剂(p = 0.793)和BPH /前列腺炎/ HG-PIN / ASAP诊断(p = 0.428)。结论:在大多数情况下,PCA3评分可被视为随时间稳定的标志物。值得注意的是,多达20%的患者具有临床相关的风险等级变化。即使未发现PCA3评分波动的可靠截止点,PCA3评分升高的患者中PCa的发生率也较高。

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