诊断时的睾酮水平:前列腺癌患者总生存期的关键预测因素

IF 1.6 Q3 UROLOGY & NEPHROLOGY
BJUI compass Pub Date : 2025-02-17 DOI:10.1002/bco2.484
Ilkka Jussila, Juha P. Ahtiainen, Eija K. Laakkonen, Pirjo Käkelä, Maisa Parviainen, Heikki Pohjolainen, Jarno Aaltonen, Ninamaria Onni, Koskimaa Mikko, Teemu J. Murtola, Heini Huhtala, Heikki Seikkula
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引用次数: 0

摘要

背景与目的前列腺癌诊断时睾酮水平与预后之间的确切关系尚不清楚。目的是确定前列腺癌诊断时血清睾酮水平是否与总生存率相关。患者与方法本研究共纳入2544例PCa患者,分为三组;正常(10.4 nmol/L)、灰色(8.0 ~ 10.4 nmol/L)和低(2.0 ~ 8.0 nmol/L)血清睾酮组。生存结局采用Kaplan-Meier曲线和Cox回归模型进行分析。结果分析显示,在单因素(HR = 1.67, 95% CI: 1.37-2.05, p < 0.001)和多因素调整(HR = 1.58, 95% CI: 1.24-1.98, p < 0.001)分析中,低睾酮水平患者的死亡风险高于正常水平患者。对糖代谢正常的患者进行敏感性分析,结果与70岁以下(HR = 1.55, 95% CI: 1.02-2.36, p < 0.001)和70岁以上(HR = 1.83, 95% CI: 1.46-2.28, p < 0.001)分层后的结果相似(HR = 1.93, CI: 1.48-2.51, p < 0.001)。与其他睾酮组相比,灰色地带组的存活率没有差异。回顾性设计限制了我们推断因果关系的能力。结论前列腺癌诊断时睾酮水平低是总生存率的独立预测因子。研究结果强调了睾酮在前列腺癌预后评估中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Testosterone levels at diagnosis: A key predictor of overall survival among patients with prostate cancer

Testosterone levels at diagnosis: A key predictor of overall survival among patients with prostate cancer

Background and Objective

The exact relationship between testosterone levels at diagnosis and prostate cancer (PCa) prognosis remains inadequately explored. The objective was to determine whether serum testosterone levels at the time of PCa diagnosis are associated with overall survival.

Patients and Methods

The study cohort involved 2544 PCa patients, divided into three groups; normal (>10.4 nmol/L), grey zone (8.0–10.4 nmol/L) and low (2.0–8.0 nmol/L) serum testosterone groups. Survival outcomes were analysed using Kaplan–Meier curves and Cox regression models.

Results

The analysis revealed an increased risk of death among patients with low testosterone levels compared to those with normal levels in uni- (HR = 1.67, 95% CI: 1.37–2.05, p < 0.001) and multivariable-adjusted (HR = 1.58, 95% CI: 1.24–1.98, p < 0.001) analysis. Sensitivity analysis on patients with normal glucose metabolism revealed similar results (HR = 1.93, CI: 1.48–2.51, p < 0.001), as well as after stratified with age below 70 years (HR = 1.55, 95% CI: 1.02–2.36, p < 0.001) and over 70 years (HR = 1.83, 95% CI: 1.46–2.28, p < 0.001.) There was no difference in survival between the grey zone compared to other testosterone groups. The retrospective design limits our ability to infer causality.

Conclusion

Low testosterone at the time of PCa diagnosis is an independent predictor of overall survival. Findings highlight the potential of testosterone for prognostic evaluation in PCa.

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CiteScore
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