Mori Kohei, Matsumoto Kazumasa, Amano Noriyuki, Koguchi Dai, Shimura Soichiro, Hagiwara Masahiro, Shimizu Yuriko, Ikeda Masaomi, Sato Yuichi, Iwamura Masatsugu
Department of Urology, Kitasato University School of Medicine, 1-15-1 Kitasato Minami-ku Sagamihara, Sagamihara 252-0374, Kanagawa, Japan.
Cancers (Basel). 2022 Mar 19;14(6):1576. doi: 10.3390/cancers14061576.
Objective: To investigate the relationship between clinicopathological findings and membranous CD155 (mCD155) or cytoplasmic CD155 (cCD155) expression in bladder cancer (BC). Methods: We retrospectively analyzed 103 patients with BC who underwent radical cystectomy between 1990 to 2015 at Kitasato University Hospital. Immunohistochemical staining was performed to evaluate CD155 expression in tumor cells. Cases with > 10% expression on the membrane or cytoplasm of tumor cells were positive. The Fisher′s exact test was used for categorical variables and the Kaplan−Meier method was used for survival outcomes. Univariate and multivariate Cox regression hazard models were used to evaluate the survival risk factors. Results: Cases that were mCD155-positive were associated with high-grade tumors (p = 0.02), nodal status (p < 0.01), and pT stage (p = 0.04). No association with any clinicopathological factor was observed in the cCD155 cases. Kaplan−Meier analysis showed that mCD155-positive cases had shorter periods of recurrence-free survival (p = 0.015) and cancer-specific survival (p = 0.005). Only nodal status was an independent predictor for both cancer-specific survival and recurrence-free survival in multivariate analysis (p = 0.02 and p < 0.01, respectively). Conclusion: mCD155 expression may be a marker of an aggressive phenotype and a poor prognosis in patients with BC.
探讨膀胱癌(BC)的临床病理特征与膜性CD155(mCD155)或胞浆CD155(cCD155)表达之间的关系。方法:我们回顾性分析了1990年至2015年期间在北里大学医院接受根治性膀胱切除术的103例BC患者。采用免疫组织化学染色评估肿瘤细胞中CD155的表达。肿瘤细胞膜或细胞质表达>10%的病例为阳性。分类变量采用Fisher精确检验,生存结局采用Kaplan-Meier法。单因素和多因素Cox回归风险模型用于评估生存风险因素。结果:mCD155阳性病例与高级别肿瘤(p = 0.02)、淋巴结状态(p < 0.01)和pT分期(p = 0.04)相关。cCD155病例未观察到与任何临床病理因素相关。Kaplan-Meier分析显示,mCD155阳性病例的无复发生存期(p = 0.015)和癌症特异性生存期(p = 0.005)较短。多因素分析中,仅淋巴结状态是癌症特异性生存和无复发生存的独立预测因素(分别为p = 0.02和p < 0.01)。结论:mCD155表达可能是BC患者侵袭性表型和不良预后的标志物。