Kriegmair M C, Wirtz R M, Worst T S, Breyer J, Ritter M, Keck B, Boehmer C, Otto W, Eckstein M, Weis C A, Hartmann A, Bolenz C, Erben P
Department of Urology, Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Stratifyer Molecular Pathology, Werthmannstraße 1, 50935, Köln, Germany.
Transl Oncol. 2018 Apr;11(2):467-476. doi: 10.1016/j.tranon.2018.02.001. Epub 2018 Feb 23.
Gene expression analyses have identified similarities between bladder and breast cancer, where clinical risk stratification is based on Her2, ESR1, PGR and Ki67 expression. The aim of the study was to assess the respective marker gene expression in patients treated with radical cystectomy for muscle-invasive bladder cancer (MIBC) and to evaluate the applicability of breast cancer subtypes for MIBC risk stratification.
MATERIALS & METHODS: 102 patients treated with radical cystectomy for MIBC were assessed. Using routine FFPE tissue and an IVD validated kit, mRNA expression was measured by single step RT-qPCR. Partition test were employed to define cut-off values for high or low marker gene expression. Association of expression with outcome was assessed using Kaplan-Meier analysis and multivariate cox regression analysis. Finally, we performed validation of our results in the MD-Anderson cohort (n=57).
Cancer specific survival (CSS) was impaired in patients with high gene expression of Her2 (P=0.0009) and ESR1 (P=0.04). In the multivariate regression model Her2 expression remained significant for the prediction of CSS (HR=2.11, CI 1.11-4.21, P=0.024). Furthermore, molecular stratification by breast cancer subgroups was significant (P=0.023) for CSS prediction. Especially the differentiation between Her2-positive and Luminal A (HR=4.41, CI 1.53-18.71, P=0.004) and Luminal B (HR=1.96, CI 0.99-4.08, P=0.053) respectively was an independent prognostic parameter for CSS. External validation resulted in comparable risk stratification with differences in fractional subgroups distribution.
Gene expression of Her2, ESR1, PGR, Ki67 and corresponding breast cancer subtypes allow a risk-stratification in MIBC, whereby Her2 overexpressing tumors reveal a particularly poor prognosis.
基因表达分析已确定膀胱癌和乳腺癌之间存在相似性,其中临床风险分层基于Her2、ESR1、PGR和Ki67表达。本研究的目的是评估接受根治性膀胱切除术治疗的肌层浸润性膀胱癌(MIBC)患者中各自标记基因的表达情况,并评估乳腺癌亚型在MIBC风险分层中的适用性。
对102例接受根治性膀胱切除术治疗的MIBC患者进行评估。使用常规福尔马林固定石蜡包埋(FFPE)组织和经体外诊断(IVD)验证的试剂盒,通过单步逆转录定量聚合酶链反应(RT-qPCR)测量mRNA表达。采用分区测试来定义高或低标记基因表达的临界值。使用Kaplan-Meier分析和多变量Cox回归分析评估表达与预后的相关性。最后,我们在MD安德森队列(n = 57)中对结果进行了验证。
Her2(P = 0.0009)和ESR1(P = 0.04)基因高表达的患者癌症特异性生存(CSS)受损。在多变量回归模型中,Her2表达对CSS的预测仍然具有显著性(风险比[HR]=2.11,置信区间[CI] 1.11 - 4.21,P = 0.024)。此外,根据乳腺癌亚组进行分子分层对CSS预测具有显著性(P = 0.023)。特别是Her2阳性与腔面A型(HR = 4.41,CI 1.53 - 18.71,P = 0.004)和腔面B型(HR = 1.96,CI 0.99 - 4.08,P = 0.053)之间的差异分别是CSS的独立预后参数。外部验证得出了可比的风险分层,但各分数亚组分布存在差异。
Her2、ESR1、PGR、Ki67的基因表达及相应的乳腺癌亚型可对MIBC进行风险分层,其中Her2过表达的肿瘤预后特别差。