Concordance of biopsy and pathologic ISUP grading in salvage radical prostatectomy patients for recurrent prostate cancer.

The Prostate Pub Date : 2022-02-01 Epub Date: 2021-11-22 DOI:10.1002/pros.24268
Felix Preisser, Christoph Würnschimmel, Randi M Pose, Alexander Heinze, Thomas Steuber, Uwe Michl, Georg Salomon, Philipp Mandel, Markus Graefen, Derya Tilki
{"title":"Concordance of biopsy and pathologic ISUP grading in salvage radical prostatectomy patients for recurrent prostate cancer.","authors":"Felix Preisser,&nbsp;Christoph Würnschimmel,&nbsp;Randi M Pose,&nbsp;Alexander Heinze,&nbsp;Thomas Steuber,&nbsp;Uwe Michl,&nbsp;Georg Salomon,&nbsp;Philipp Mandel,&nbsp;Markus Graefen,&nbsp;Derya Tilki","doi":"10.1002/pros.24268","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To investigate the concordance of biopsy and pathologic International Society of Urological Pathology (ISUP) grading in salvage radical prostatectomy (SRP) patients for recurrent prostate cancer.</p><p><strong>Methods: </strong>Within a high-volume center database, we identified patients who underwent SRP for recurrent prostate cancer (PCa) between 2004 and 2020. Upgrading, downgrading, concordance, and any discordance between posttreatment biopsy ISUP and ISUP at SRP were tested. Logistic regression models were used to predict ISUP upgrading and ISUP discordance. Models were adjusted for prostatic specific antigen before SRP, age at surgery, initial prostatic specific antigen (PSA), type of primary treatment, time from primary PCa diagnosis to SRP, number of positive cores at biopsy, and original Gleason score.</p><p><strong>Results: </strong>Overall, 184 patients with available biopsy and pathologic ISUP grading were identified. Of those, 17.4% (n = 32), 40.8% (n = 75), 19.6% (n = 36), and 22.2% (n = 41) harbored biopsy ISUP 1, ISUP 2, ISUP 3, and ISUP 4-5 grading, respectively. Pathologic ISUP 1, ISUP 2, ISUP 3, and ISUP 4-5 grading was recorded in 6.0% (n = 11), 40.8% (n = 75), 32.1% (n = 59), and 21.2% (n = 39), respectively. Median PSA before SRP was 5.5 ng/ml (interquartile range [IQR]: 3.1-8.1 ng/ml), median age at SRP was 65.1 years (IQR:60.7-69.4 years) and median time from original PCa diagnosis to SRP was 47 months (IQR: 27.3-85.2 months). Concordance of biopsy and pathologic ISUP was identified in 45.1% (n = 83). Conversely, any ISUP discordance, upgrading and downgrading of at least one ISUP group was identified in 54.9% (n = 101), 35.3% (n = 65), and 19.6% (n = 36). In logistic models, none of the preoperative characteristics was associated with upgrading or ISUP discordance (all p > 0.1).</p><p><strong>Conclusion: </strong>Discordance between biopsy and pathologic ISUP grading is common at SRP. However, in 45% of SRP cases biopsy ISUP is capable to predict pathologic ISUP. Further studies are necessary to identify characteristics for ISUP upgrading at SRP.</p>","PeriodicalId":501684,"journal":{"name":"The Prostate","volume":" ","pages":"254-259"},"PeriodicalIF":0.0000,"publicationDate":"2022-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Prostate","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/pros.24268","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/11/22 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Purpose: To investigate the concordance of biopsy and pathologic International Society of Urological Pathology (ISUP) grading in salvage radical prostatectomy (SRP) patients for recurrent prostate cancer.

Methods: Within a high-volume center database, we identified patients who underwent SRP for recurrent prostate cancer (PCa) between 2004 and 2020. Upgrading, downgrading, concordance, and any discordance between posttreatment biopsy ISUP and ISUP at SRP were tested. Logistic regression models were used to predict ISUP upgrading and ISUP discordance. Models were adjusted for prostatic specific antigen before SRP, age at surgery, initial prostatic specific antigen (PSA), type of primary treatment, time from primary PCa diagnosis to SRP, number of positive cores at biopsy, and original Gleason score.

Results: Overall, 184 patients with available biopsy and pathologic ISUP grading were identified. Of those, 17.4% (n = 32), 40.8% (n = 75), 19.6% (n = 36), and 22.2% (n = 41) harbored biopsy ISUP 1, ISUP 2, ISUP 3, and ISUP 4-5 grading, respectively. Pathologic ISUP 1, ISUP 2, ISUP 3, and ISUP 4-5 grading was recorded in 6.0% (n = 11), 40.8% (n = 75), 32.1% (n = 59), and 21.2% (n = 39), respectively. Median PSA before SRP was 5.5 ng/ml (interquartile range [IQR]: 3.1-8.1 ng/ml), median age at SRP was 65.1 years (IQR:60.7-69.4 years) and median time from original PCa diagnosis to SRP was 47 months (IQR: 27.3-85.2 months). Concordance of biopsy and pathologic ISUP was identified in 45.1% (n = 83). Conversely, any ISUP discordance, upgrading and downgrading of at least one ISUP group was identified in 54.9% (n = 101), 35.3% (n = 65), and 19.6% (n = 36). In logistic models, none of the preoperative characteristics was associated with upgrading or ISUP discordance (all p > 0.1).

Conclusion: Discordance between biopsy and pathologic ISUP grading is common at SRP. However, in 45% of SRP cases biopsy ISUP is capable to predict pathologic ISUP. Further studies are necessary to identify characteristics for ISUP upgrading at SRP.

复发性前列腺癌根治性前列腺切除术患者活检和病理ISUP分级的一致性。
目的:探讨复发性前列腺癌根治性前列腺切除术(SRP)患者活检结果与国际泌尿病理学会(ISUP)病理分级的一致性。方法:在一个大容量的中心数据库中,我们确定了2004年至2020年间因复发性前列腺癌(PCa)接受SRP治疗的患者。测试了治疗后活检ISUP和SRP ISUP之间的升级、降级、一致性和任何不一致。采用Logistic回归模型对ISUP升级和ISUP不一致性进行预测。根据SRP前的前列腺特异性抗原、手术年龄、初始前列腺特异性抗原(PSA)、初次治疗类型、从原发性PCa诊断到SRP的时间、活检阳性核心数和原始Gleason评分对模型进行调整。结果:总的来说,184例可用的活检和病理ISUP分级被确定。其中,17.4% (n = 32), 40.8% (n = 75), 19.6% (n = 36)和22.2% (n = 41)的活检分别为ISUP 1, ISUP 2, ISUP 3和ISUP 4-5分级。病理ISUP 1、ISUP 2、ISUP 3和ISUP 4-5分级分别为6.0% (n = 11)、40.8% (n = 75)、32.1% (n = 59)和21.2% (n = 39)。SRP前的中位PSA为5.5 ng/ml(四分位间距[IQR]: 3.1-8.1 ng/ml), SRP时的中位年龄为65.1岁(IQR:60.7-69.4岁),从原始PCa诊断到SRP的中位时间为47个月(IQR: 27.3-85.2个月)。45.1% (n = 83)的活检和病理ISUP一致。相反,在54.9% (n = 101)、35.3% (n = 65)和19.6% (n = 36)中发现了至少一个ISUP组的任何ISUP不一致、升级和降级。在logistic模型中,术前特征均与升级或ISUP不一致无关(均p > 0.1)。结论:在SRP中,活检和病理ISUP分级之间的不一致是常见的。然而,在45%的SRP病例中,活检ISUP能够预测病理性ISUP。需要进一步的研究来确定ISUP在SRP升级的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信