Department of Urology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Int J Urol. 2011 Sep;18(9):616-29. doi: 10.1111/j.1442-2042.2011.02809.x. Epub 2011 Jul 20.
Urothelial carcinoma of the bladder (UCB) is an especially complex and heterogeneous disease with a broad spectrum of histologic findings and potentially lethal behavior. Despite advances in surgical techniques, as well as intravesical and systemic therapies, up to 30% of patients with non-muscle-invasive UCB and 50% of patients with muscle-invasive UCB experience disease progression, recurrence, and eventual death. Standard prognostic features, such as pathologic stage and grade, have limited ability to predict the outcomes of this heterogeneous population. Current risk-stratification algorithms using clinical and pathologic parameters are limited in their prognostic ability. Molecular medicine holds the promise that clinical outcomes will be improved by more accurate prognostication and directing therapy towards the mechanisms and targets associated with the growth of an individual patient's tumor. Immunohistochemical analysis of biomarker expression has provided insight into the molecular pathogenesis of UCB and offers the potential for improving clinical decision making. Numerous candidate immunohistochemical biomarkers for patients with UCB have been identified, with those relating to the cell cycle and apoptosis/cell proliferation being the most extensively studied. The present review discusses the most promising immunohistochemical biomarkers. Special attention is paid to recent data from a multi-institutional collaboration that has implemented a regulated, phased biomarker discovery and validation pathway. Because UCB tumorigenesis and progression is a process involving multiple genetic and epigenetic alterations, multiple biomarkers need to be integrated into a prognostic signature to accurately predict outcomes. There is no doubt that biomarkers will eventually guide our clinical decision making regarding follow-up scheduling and treatment choice.
膀胱癌(UCB)是一种特别复杂和异质的疾病,具有广泛的组织学发现和潜在致命的行为。尽管手术技术、膀胱内和全身治疗有所进步,但高达 30%的非肌肉浸润性 UCB 患者和约 50%的肌肉浸润性 UCB 患者会出现疾病进展、复发和最终死亡。标准的预后特征,如病理分期和分级,对预测这种异质人群的结果能力有限。目前使用临床和病理参数的风险分层算法在预测能力方面存在局限性。分子医学有望通过更准确的预后判断,并针对与个体患者肿瘤生长相关的机制和靶点指导治疗,从而改善临床结果。生物标志物表达的免疫组织化学分析为 UCB 的分子发病机制提供了深入了解,并为改善临床决策提供了潜力。已经鉴定出许多用于 UCB 患者的候选免疫组织化学生物标志物,其中与细胞周期和凋亡/细胞增殖相关的标志物研究最为广泛。本综述讨论了最有前途的免疫组织化学生物标志物。特别关注来自多机构合作的最新数据,该合作实施了受监管的分阶段生物标志物发现和验证途径。由于 UCB 肿瘤发生和进展是一个涉及多个遗传和表观遗传改变的过程,因此需要将多个生物标志物整合到预后标志中,以准确预测结果。毫无疑问,生物标志物最终将指导我们关于随访计划和治疗选择的临床决策。