活组织检查 1 级前列腺癌和高危特征男性的癌症相关死亡风险:欧洲多机构研究

IF 3.2 3区 医学 Q1 UROLOGY & NEPHROLOGY
Daimantas Milonas , Alexander Giesen , Tim Muilwijk , Charlotte Soenens , Gaëtan Devos , Zilvinas Venclovas , Alberto Briganti , Paolo Gontero , R. Jeffrey Karnes , Piotr Chlosta , Frank Claessens , Gert De Meerleer , Wouter Everaerts , Markus Graefen , Giansilvio Marchioro , Rafael Sanchez-Salas , Bertrand Tombal , Henk Van Der Poel , Hendrik Van Poppel , Martin Spahn , Steven Joniau
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引用次数: 0

摘要

国际泌尿病理学会第 1 组(GG 1)前列腺癌(PCa)通常被认为无足轻重,最近还有人认为它甚至应被视为 "非癌症"。我们评估了活检为 GG 1 组 PCa(bGG 1)且具有高危特征(前列腺特异性抗原 [PSA] 20 ng/ml 和/或 cT3-4 分期)的患者的预后,以挑战 bGG 1 组 PCa 病程均为良性的假设。我们使用了多机构 EMPaCT 数据库,其中包括 9508 例接受手术的高危 PCa 患者的数据。我们将 bGG 1 PCa 患者(n = 848)纳入分析,并根据 PSA >20 ng/ml、cT3-4 分期或两者将其分为三组。估计总人群的10年癌症特异性生存率(CSS)为96%,PSA>20纳克/毫升和cT3-4分期组为88%,仅PSA>20纳克/毫升组为97%,仅cT3-4分期组为98%。在病理诊断为GG 1 PCa(502人)和2005年后活检诊断为GG 1 PCa(253人)的亚组中,CSS结果相似。研究的局限性包括缺乏磁共振成像(MRI)分期和磁共振成像靶向活检。总之,GG 1、PSA 为 20 ng/ml 或 cT3-4 分期的患者术后死于癌症的风险较低。然而,GG 1 PCa 患者同时伴有 PSA >20 纳克/毫升和 cT3-4 分期的癌症特异性死亡风险较高,因此应讨论针对该亚组患者的积极治疗。同时具有这两种高危因素的男性死于前列腺癌的风险较高。对于这部分患者,应该讨论积极治疗的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of Cancer-related Death for Men with Biopsy Grade Group 1 Prostate Cancer and High-risk Features: A European Multi-institutional Study

International Society of Urological Pathology grade group 1 (GG 1) prostate cancer (PCa) is generally considered insignificant, with recent suggestions that it should even be considered as “noncancerous”. We evaluated outcomes for patients with GG 1 PCa on biopsy (bGG 1) and high-risk features (prostate-specific antigen [PSA] >20 ng/ml and/or cT3–4 stage) to challenge the hypothesis that every case of bGG 1 PCa has a benign disease course. We used the multi-institutional EMPaCT database, which includes data for 9508 patients with high-risk PCa undergoing surgery. We included patients with bGG 1 PCa (n = 848) in our analysis and divided them into three groups according to PSA >20 ng/ml, cT3–4 stage, or both. The estimated 10-yr cancer-specific survival (CSS) rate was 96% in the overall population, 88% in the group with both PSA >20 ng/ml and cT3–4 stage, 97% in the group with PSA >20 ng/ml alone, and 98% in the group with cT3–4 stage alone. Similar CSS outcomes were found in subgroups with GG 1 PCa on pathology (n = 502) and with GG 1 on biopsy diagnosed after 2005 (n = 253). Study limitations include the lack of magnetic resonance imaging (MRI) staging and MRI-targeted biopsies. In conclusion, patients with GG 1 and either PSA >20 ng/ml or cT3–4 stage have a low risk of dying from their cancer after surgery. However, patients with GG 1 PCa and both PSA >20 ng/ml and cT3–4 stage are at higher risk of cancer-specific mortality and active treatment should be discussed for this subgroup.

Patient summary

We assessed outcomes for patients diagnosed with low-grade prostate cancer on biopsy who also had one or two factors associated with high risk disease. Men with both of those risk factors had a higher risk of dying from their prostate cancer. Active treatment should be discussed for this subgroup of patients.

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来源期刊
European Urology Open Science
European Urology Open Science UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
4.00%
发文量
1183
审稿时长
49 days
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