Ahmad Ardalan E, Mohammed Aza, Bhindi Bimal, Richard Patrick O, Fadaak Kamel, Leão Ricardo, Finelli Antonio, Fleshner Neil E, Kulkarni Girish S
Division of Urology, Department of Surgery, University Health Network, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
Department of Urology, Luton and Dunstable University Hospital, Luton, UK.
Cancer Manag Res. 2019 Nov 29;11:10043-10050. doi: 10.2147/CMAR.S226174. eCollection 2019.
Elevated adipokines in patients with obesity and metabolic syndrome have been linked to increased risk of prostate cancer (PCa). The association between select serum adipokines and the outcome of prostate biopsies alone and in combination with clinical parameters at different early stages of PCa was investigated.
Clinical data and serum adipokines were retrieved from three retrospective cohorts representing men at different points in PCa detection: 1. Subjects with no prior biopsies (n=1061), 2. subjects with a prior negative biopsy (REDUCE trial, control arm) (n=1209), 3. subjects with low-risk PCa on active surveillance (AS) (n=154). Adipokines were chosen based on an unpublished pilot study and included: Resistin, Tumor Necrosis Factor-α, Interleukin-6, Monocyte Chemoattractant Protein-1, Hepatocyte Growth Factor, and Nerve Growth Factor. The primary outcome was the absence of PCa on biopsy and the secondary outcome was diagnosis of low-risk PCa fitting the criteria for continuing AS. Logistic regression analysis was used to assess the association of adipokines and negative and/or low-risk PCa at prostate biopsy.
In men with no prior prostate biopsy or with prior negative biopsy, adipokines were not predictors of prostate biopsy outcomes on multivariable regression analysis controlling for known clinical variables. In the AS cohort, MCP-1 and Resistin were significant predictors of biopsy outcome on multivariable analysis (OR 0.20, 95% CI: 0.05-0.85, p= 0.03 & OR 0.30, 95% CI: 0.10 -0.86, p= 0.03).
Our findings do not support a strong role for adipokines for predicting the outcome of prostate biopsies at any early stage in PCa diagnosis.
肥胖和代谢综合征患者体内升高的脂肪因子与前列腺癌(PCa)风险增加有关。本研究调查了特定血清脂肪因子与前列腺活检结果之间的关联,以及它们与PCa不同早期阶段临床参数相结合的情况。
从三个回顾性队列中获取临床数据和血清脂肪因子,这些队列代表了处于PCa检测不同阶段的男性:1. 未进行过活检的受试者(n = 1061);2. 之前活检结果为阴性的受试者(REDUCE试验,对照组)(n = 1209);3. 接受主动监测(AS)的低风险PCa受试者(n = 154)。基于一项未发表的初步研究选择脂肪因子,包括:抵抗素、肿瘤坏死因子-α、白细胞介素-6、单核细胞趋化蛋白-1、肝细胞生长因子和神经生长因子。主要结局是活检时未发现PCa,次要结局是诊断为符合继续AS标准的低风险PCa。采用逻辑回归分析评估脂肪因子与前列腺活检时阴性和/或低风险PCa的关联。
在未进行过前列腺活检或之前活检结果为阴性的男性中,在控制已知临床变量的多变量回归分析中,脂肪因子不是前列腺活检结果的预测指标。在AS队列中,多变量分析显示MCP-1和抵抗素是活检结果的显著预测指标(OR 0.20,95% CI:0.05 - 0.85,p = 0.03;OR 0.30,95% CI:0.10 - 0.86,p = 0.03)。
我们的研究结果不支持脂肪因子在PCa诊断的任何早期阶段预测前列腺活检结果中起重要作用。