前列腺癌伴高级别前列腺上皮内瘤变的临床特征及预后。

Korean Journal of Urology Pub Date : 2015-08-01 Epub Date: 2015-07-24 DOI:10.4111/kju.2015.56.8.565
Donghyun Lee, Chunwoo Lee, Taekmin Kwon, Dalsan You, In Gab Jeong, Jun Hyuk Hong, Hanjong Ahn, Choung-Soo Kim
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引用次数: 5

摘要

目的:探讨前列腺癌(PCa)合并高级别前列腺上皮内瘤变(HGPIN)的临床特征及生化复发(BCR)。材料和方法:我们回顾性分析了2011年至2012年在牙山医疗中心接受根治性前列腺切除术治疗前列腺癌的893例患者的医疗记录;其中752例患者未接受新辅助或辅助治疗,且随访1年以上。将该队列分为两组:有hgpin和没有hgpin的患者,并比较他们的特征。采用Cox比例风险模型分析影响BCR的因素。结果:652例患者(86.7%)有HGPIN。两组术前因素年龄(p=0.369)、术前前列腺特异性抗原浓度(p=0.234)差异无统计学意义。HGPIN患者Gleason评分较高(p=0.012),多发肿瘤发生率较高(p=0.013),神经周围侵犯发生率较高(p=0.012),但两组术后其他病理特征无显著差异。两组间BCR差异无统计学意义(13.0% vs. 11.5%, p=0.665), HGPIN与BCR无相关性(p=0.745)。结论:与不含HGPIN的PCa患者相比,HGPIN患者Gleason评分更高,多发肿瘤发生率更高,神经周围侵袭程度更高。HGPIN的存在并不是BCR的独立预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Clinical features and prognosis of prostate cancer with high-grade prostatic intraepithelial neoplasia.

Purpose: To evaluate the clinical features and biochemical recurrence (BCR) in prostate cancer (PCa) with high-grade prostatic intraepithelial neoplasia (HGPIN).

Materials and methods: We retrospectively analyzed the medical records of 893 patients who underwent a radical prostatectomy for PCa between 2011 and 2012 at Asan Medical Center; 752 of these patients who did not receive neoadjuvant or adjuvant therapy and were followed up for more than 1 year were included. The cohort was divided into two groups-patients with and without HGPIN-and their characteristics were compared. The Cox proportional hazards model was used to analyze factors affecting BCR.

Results: In total, 652 study patients (86.7%) had HGPIN. There were no significant differences in preoperative factors between the two groups, including age (p=0.369) and preoperative prostate-specific antigen concentration (p=0.234). Patients with HGPIN had a higher Gleason score (p=0.012), more frequent multiple tumor (p=0.013), and more perineural invasion (p=0.012), but no other postoperative pathologic characteristics were significantly different between the two groups. There were no significant differences in BCR (13.0% vs. 11.5%, p=0.665) and HGPIN was not associated with BCR (p=0.745). In multivariate analysis, only the T stage (p<0.001) was associated with BCR.

Conclusions: PCa patients with HGPIN have a higher Gleason score, more frequent multiple tumors, and more perineural invasion than those without HGPIN. The presence of HGPIN is not an independent predictor of BCR.

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