Prencipe Maria, Fabre Aurelie, Murphy Thomas Brendan, Vargyas Eszter, O'Neill Amanda, Bjartell Anders, Tasken Kristin Austlid, Grytli Helene H, Svindland Aud, Berge Viktor, Eri Lars M, Gallagher William, Watson R William
UCD School of Medicine, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin, Ireland.
Department of Pathology, St Vincent's University Hospital, Dublin, Ireland.
Prostate. 2018 Jul;78(10):724-730. doi: 10.1002/pros.23516. Epub 2018 Apr 2.
Up to a third of prostate cancer patients fail curative treatment strategies such as surgery and radiation therapy in the form of biochemical recurrence (BCR) which can be predictive of poor outcome. Recent clinical trials have shown that men experiencing BCR might benefit from earlier intervention post-radical prostatectomy (RP). Therefore, there is an urgent need to identify earlier prognostic biomarkers which will guide clinicians in making accurate diagnosis and timely decisions on the next appropriate treatment. The objective of this study was to evaluate Serum Response Factor (SRF) protein expression following RP and to investigate its association with BCR.
SRF nuclear expression was evaluated by immunohistochemistry (IHC) in TMAs across three international radical prostatectomy cohorts for a total of 615 patients. Log-rank test and Kaplan-Meier analyses were used for BCR comparisons. Stepwise backwards elimination proportional hazard regression analysis was used to explore the significance of SRF in predicting BCR in the context of other clinical pathological variables. Area under the curve (AUC) values were generated by simulating repeated random sub-samples.
Analysis of the immunohistochemical staining of benign versus cancer cores showed higher expression of nuclear SRF protein expression in cancer cores compared with benign for all the three TMAs analysed (P < 0.001, n = 615). Kaplan-Meier curves of the three TMAs combined showed that patients with higher SRF nuclear expression had a shorter time to BCR compared with patients with lower SRF expression (P < 0.001, n = 215). Together with pathological T stage T3, SRF was identified as a predictor of BCR using stepwise backwards elimination proportional hazard regression analysis (P = 0.0521). Moreover ROC curves and AUC values showed that SRF was better than T stage in predicting BCR at year 3 and 5 following radical prostatectomy, the combination of SRF and T stage had a higher AUC value than the two taken separately.
SRF assessment by IHC following RP could be useful in guiding clinicians to better identify patients for appropriate follow-up and timely treatment.
高达三分之一的前列腺癌患者会以生化复发(BCR)的形式出现手术和放射治疗等根治性治疗策略失败的情况,而BCR可预示不良预后。近期临床试验表明,经历BCR的男性可能会从根治性前列腺切除术后(RP)的早期干预中获益。因此,迫切需要识别更早的预后生物标志物,以指导临床医生进行准确诊断并及时决定下一步合适的治疗方案。本研究的目的是评估RP后血清反应因子(SRF)蛋白的表达情况,并研究其与BCR的关联。
通过免疫组织化学(IHC)对来自三个国际根治性前列腺切除术队列的615例患者的组织微阵列(TMA)进行SRF核表达评估。采用对数秩检验和Kaplan-Meier分析进行BCR比较。采用逐步向后消除比例风险回归分析,在其他临床病理变量的背景下探讨SRF在预测BCR中的意义。通过模拟重复随机子样本生成曲线下面积(AUC)值。
对良性与癌性核心的免疫组织化学染色分析显示,在分析的所有三个TMA中,癌性核心中核SRF蛋白表达均高于良性核心(P < 0.001,n = 615)。三个TMA合并后的Kaplan-Meier曲线显示,SRF核表达较高的患者与SRF表达较低的患者相比,BCR发生时间更短(P < 0.001,n = 215)。通过逐步向后消除比例风险回归分析,SRF与病理T分期T3一起被确定为BCR的预测指标(P = 0.0521)。此外,ROC曲线和AUC值显示,在根治性前列腺切除术后第3年和第5年预测BCR时,SRF比T分期更好,SRF和T分期联合使用时的AUC值高于单独使用两者。
RP后通过IHC评估SRF可能有助于指导临床医生更好地识别适合进行适当随访和及时治疗的患者。