Poletajew Sławomir, Fus Łukasz, Ilczuk Tomasz, Wojcieszak Piotr, Sękowska Małgorzata, Krajewski Wojciech, Wasiutyński Aleksander, Górnicka Barbara, Radziszewski Piotr
Department of Urology, Medical University of Warsaw, Warsaw, Poland.
Department of Pathology, Medical University of Warsaw, Warsaw, Poland.
Cent Eur J Immunol. 2018;43(4):421-427. doi: 10.5114/ceji.2018.79509. Epub 2018 Dec 31.
The aim of the study was to validate the value of E-cadherin and -catenin expression and to test an alternative prognostic marker, epithelial membrane antigen (EMA).
Forty-nine consecutive patients with primary stage T1 non-muscle-invasive bladder cancer (NMIBC) were enrolled in this study. Tissue specimens were stained with the following mouse anti-human antibodies: anti-E-cadherin, anti--catenin, and anti-EMA. Reaction intensity within cancer cells was assessed according to the immunoreactive score (IRS). Finally, the association between the expression of selected proteins and patient survival was assessed.
The mean follow-up was 34.8 months. Recurrence-free survival, progression-free survival, and overall survival (OS) were 47.5%, 72.5%, and 72.5%, respectively. Differences in the IRS for -catenin and EMA were found clinically, but were not statistically significant in prediction of the risk of disease progression (p > 0.05). No difference in protein expression was observed regarding the risk of recurrence, OS, or cancer-specific mortality (p > 0.05). Stratification of patients based on the IRS into three groups (poor, moderate, and intensive reaction) failed to identify a prognostic marker among the tested proteins (p > 0.05).
Expression of E-cadherin, -catenin, and EMA cannot reliably predict survival in patients with high-risk NMIBC. Further searches are needed to identify tissue markers of progression and recurrence in NMIBC.
本研究旨在验证E-钙黏蛋白和β-连环蛋白表达的价值,并测试一种替代预后标志物——上皮膜抗原(EMA)。
49例连续的原发性T1期非肌层浸润性膀胱癌(NMIBC)患者纳入本研究。组织标本用以下小鼠抗人抗体染色:抗E-钙黏蛋白、抗β-连环蛋白和抗EMA。根据免疫反应评分(IRS)评估癌细胞内的反应强度。最后,评估所选蛋白表达与患者生存率之间的关联。
平均随访时间为34.8个月。无复发生存率、无进展生存率和总生存率(OS)分别为47.5%、72.5%和72.5%。临床上发现β-连环蛋白和EMA的IRS存在差异,但在预测疾病进展风险方面无统计学意义(p>0.05)。在复发风险、OS或癌症特异性死亡率方面,未观察到蛋白表达的差异(p>0.05)。根据IRS将患者分为三组(反应差、中等和强烈),未能在所测试的蛋白中识别出预后标志物(p>0.05)。
E-钙黏蛋白、β-连环蛋白和EMA的表达不能可靠地预测高危NMIBC患者的生存率。需要进一步寻找NMIBC进展和复发的组织标志物。