Suppr超能文献

非典型小腺泡增生(ASAP):ASAP是否需要重复活检?一项多机构综述。

Atypical small acinar proliferation (ASAP): Is a repeat biopsy necessary ASAP? A multi-institutional review.

作者信息

Leone A, Gershman B, Rotker K, Butler C, Fantasia J, Miller A, Afiadata A, Amin A, Zhou A, Jiang Z, Sebo T, Mega A, Schiff S, Pareek G, Golijanin D, Yates J, Karnes R J, Renzulli J

机构信息

Division of Urology, Rhode Island Hospital, Providence, RI, USA.

Division of Urology, The Warren Alpert Medical School of Brown University, Providence, RI, USA.

出版信息

Prostate Cancer Prostatic Dis. 2016 Mar;19(1):68-71. doi: 10.1038/pcan.2015.52. Epub 2015 Nov 17.

Abstract

BACKGROUND

Atypical small acinar proliferation (ASAP) occurs in approximately 5% of prostate biopsies. Approximately 30-40% of patients with ASAP may develop prostate cancer (PCa) within a 5-year period. Current guidelines recommend a repeat biopsy within 3-6 months after the initial diagnosis. Our objective was to examine the association between ASAP and subsequent diagnosis of high-grade PCa and to evaluate the need for immediate repeat biopsy.

METHODS

A retrospective multi-institutional review identified 264 patients who underwent prostate biopsy from 2000 to 2013 (Brown), 2008 to 2013 (University of Massachusetts) and 1994 to 2005 (Mayo) and were diagnosed with ASAP. Patients underwent transrectal ultrasound-guided biopsies for elevated PSA and/or abnormal digital rectal exam. Clinicopathologic features were assessed, including rates of subsequent PCa detection of any high-grade (Gleason 7-10) PCa. Comparison was made between those with subsequent PCa on repeat biopsy and those with benign repeat pathology.

RESULTS

All 264 patients included underwent repeat biopsy with a median follow-up of 5.4 years (interquartile range: 4.6, 6.7). Of these patients, 89 (34%) were subsequently diagnosed with PCa including 21 (8%) with high-grade PCa. Pre-biopsy PSA was higher among patients subsequently diagnosed with (6.7 vs 5.8, P<0.001). Of those diagnosed with subsequent PCa, 69/89 (78%) had less than or equal to Gleason 3+3 disease and only 15/89 (17%) had Gleason 7 and 6/89 (6%) revealed Gleason ⩾8-10. Radical prostatectomy was performed on 36/89 (40%) patients. Surgical pathology revealed 11 patients ⩾Gleason 8-10 PCa.

CONCLUSIONS

Although 34% of patients with an initial diagnosis of ASAP who had repeat biopsy were subsequently diagnosed with PCa only, only 22% (8% of the total cohort) were found to have high-grade disease. Higher PSA was associated with increased risk of identifying PCa on repeat biopsy. These findings suggest that immediate repeat biopsy may be omitted in the majority of men with ASAP.

摘要

背景

非典型小腺泡增生(ASAP)在约5%的前列腺活检中出现。ASAP患者中约30 - 40%可能在5年内发展为前列腺癌(PCa)。当前指南建议在初次诊断后3 - 6个月内重复活检。我们的目的是研究ASAP与后续高级别PCa诊断之间的关联,并评估立即重复活检的必要性。

方法

一项回顾性多机构研究确定了264例在2000年至2013年(布朗)、2008年至2013年(马萨诸塞大学)以及1994年至2005年(梅奥)期间接受前列腺活检并被诊断为ASAP的患者。患者因PSA升高和/或直肠指检异常接受经直肠超声引导下活检。评估临床病理特征,包括后续任何高级别(Gleason 7 - 10)PCa的检出率。对重复活检后诊断为PCa的患者与良性重复病理的患者进行比较。

结果

所有264例纳入患者均接受了重复活检,中位随访时间为5.4年(四分位间距:4.6,6.7)。在这些患者中,89例(34%)随后被诊断为PCa,其中21例(8%)为高级别PCa。后续诊断为PCa的患者活检前PSA较高(6.7对5.8,P<0.001)。在后续诊断为PCa的患者中,69/89(78%)的Gleason评分小于或等于3 + 3,只有15/89(17%)为Gleason 7,6/89(6%)为Gleason⩾8 - 10。36/89(40%)例患者接受了根治性前列腺切除术。手术病理显示11例患者为⩾Gleason 8 - 10的PCa。

结论

虽然最初诊断为ASAP且接受重复活检的患者中34%随后仅被诊断为PCa,但仅22%(占总队列的8%)被发现患有高级别疾病。较高的PSA与重复活检时发现PCa的风险增加相关。这些发现表明,大多数ASAP男性患者可能无需立即重复活检。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验