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根据接受促性腺激素释放激素激动剂治疗的非转移性前列腺癌男性的 PSA 反应,评估去势抵抗性前列腺癌和前列腺癌死亡的时间。

Time to castration-resistant prostate cancer and prostate cancer death according to PSA response in men with non-metastatic prostate cancer treated with gonadotropin releasing hormone agonists.

机构信息

Department of Urology, Ryhov Hospital, Jönköping, Sweden.

Department of Mathematics, Uppsala University, Uppsala, Sweden.

出版信息

Scand J Urol. 2022 Jun;56(3):169-175. doi: 10.1080/21681805.2022.2070275. Epub 2022 May 12.

Abstract

To predict castration-resistant prostate cancer (CRPC) and prostate cancer (Pca) death by use of clinical variables at Pca diagnosis and PSA levels after start of gonadotropin-releasing hormone agonists (GnRH) in men with non-metastatic castration sensitive prostate cancer (nmCSPC). PSA values for 1603 men with nmCSPC in the National Prostate Cancer Register of Sweden who received GnRH as primary treatment were retrieved from Uppsala-Örebro PSA Cohort and Stockholm PSA and Biopsy Register. All men had measured PSA before () and 3-6 months after () date of start of GnRH. Unadjusted and adjusted Cox models were used to predict CRPC by PSA levels. PSA levels and ISUP grade were used to construct a risk score to stratify men by tertiles according to risk of CRPC and Pca death. 788 (49%) men reached CRPC and 456 (28%) died of Pca during follow-up. predicted CRPC regardless of . CRPC risk increased with higher , HR 4.7 (95% CI: 3.4-6.7) for PSA > 16 ng/mL vs 0-0.25 ng/mL and with ISUP grade, HR 3.7 (95%: 2.5-5.4) for ISUP 5 vs ISUP 1. Risk of Pca death in men above top vs bellow bottom tertile of and ISUP grade was HR 4.1 (95% CI: 3.0-5.5). A risk score based on and ISUP grade could be used for early identification of a target group for future clinical trials on additional therapy to GnRH.

摘要

在非转移性去势敏感前列腺癌(nmCSPC)男性中,使用前列腺癌诊断时的临床变量和开始使用促性腺激素释放激素激动剂(GnRH)后的 PSA 水平预测去势抵抗性前列腺癌(CRPC)和前列腺癌(Pca)死亡。从乌普萨拉-厄勒布鲁 PSA 队列和斯德哥尔摩 PSA 和活检登记处检索了瑞典国家前列腺癌登记处中 1603 名接受 GnRH 作为主要治疗的 nmCSPC 男性的 PSA 值。所有男性在 GnRH 开始日期之前()和之后 3-6 个月()均测量了 PSA。使用未经调整和调整的 Cox 模型根据 PSA 水平预测 CRPC。使用 PSA 水平和 ISUP 分级构建风险评分,根据 CRPC 和 Pca 死亡风险将男性分为三分位。788(49%)名男性达到 CRPC,456(28%)名男性在随访期间死于 Pca。即使在调整了 PSA 水平后,也可以预测 CRPC,。CRPC 风险随着 PSA 的升高而增加,PSA>16ng/mL 与 0-0.25ng/mL 相比,HR 为 4.7(95%CI:3.4-6.7),ISUP 分级为 5 与 ISUP 1 相比,HR 为 3.7(95%CI:2.5-5.4)。位于 PSA 和 ISUP 分级的 top 三分位以上与位于 bottom 三分位以下的男性相比,Pca 死亡的风险为 HR 4.1(95%CI:3.0-5.5)。基于 PSA 和 ISUP 分级的风险评分可用于早期确定目标人群,以便对 GnRH 后的额外治疗进行临床试验。

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