Tassinari Elisa, Mollica Veronica, Nuvola Giacomo, Marchetti Andrea, Rosellini Matteo, Massari Francesco
Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Department of Experimental, Diagnostic and Specialty Medicine, S.Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy.
Cancer Manag Res. 2022 Jun 13;14:1945-1960. doi: 10.2147/CMAR.S287904. eCollection 2022.
Urothelial carcinoma (UC) is a frequently diagnosed tumor and an important cause of cancer deaths worldwide. Until a few years ago, despite the unquestioned role of platinum-based chemotherapy, therapeutic choices beyond the first line were limited and related to unsatisfactory outcomes. Metastatic UC has always been associated with a poor prognosis, with overall survival only slightly above a year. In the recent past, huge progress has been made in our understanding of the molecular and genomic disease characteristics, to enable stratification of patients in terms of prognosis and treatment responses. Unfortunately, we still do not have the perfect combination of clinical biomarkers to tailor the optimal treatment for each patient, despite making several efforts in this direction. The therapeutic arsenal has been augmented by immune checkpoint inhibitors (ICIs), which nowadays represent the backbone of the second-line setting. Equally revolutionary was the FDA's approval of erdafitinib, a potent fibroblast growth factor receptor (FGFR) inhibitor, the use of which is reserved for patients whose tumor harbors specific FGF pathway alterations. Recently, the therapeutic landscape of metastatic UC has been enhanced by the introduction of novel compounds, consisting of antibody-drug conjugates (ADCs). Enfortumab vedotin is an antibody targeting nectin-4, a cell adhesion molecule highly expressed in UC, conjugated to monomethyl auristatin E (MMAE), a microtubule-disrupting agent. Sacituzumab govitecan is a humanized monoclonal antibody targeting Trop-2, a transmembrane glycoprotein, conjugated to the active metabolite of irinotecan. These two compounds have received accelerated approval by the FDA in patients pretreated with platinum-based chemotherapy and immunotherapy. Several ongoing trials are investigating the role of ICIs combined with chemotherapy, antiangiogenic drugs, or other ICIs, as well as the efficacy of PARP inhibitors and target therapies, hoping to provide information for some important unmet needs. In this review, we aim to evaluate the current potential treatment options after first-line chemotherapy.
尿路上皮癌(UC)是一种常见的诊断肿瘤,也是全球癌症死亡的重要原因。直到几年前,尽管铂类化疗的作用毋庸置疑,但一线治疗之外的治疗选择有限,且疗效不尽人意。转移性UC一直与预后不良相关,总生存期仅略高于一年。最近,我们对该疾病的分子和基因组特征的理解取得了巨大进展,从而能够根据预后和治疗反应对患者进行分层。不幸的是,尽管在这方面做出了多项努力,但我们仍未找到完美的临床生物标志物组合来为每位患者量身定制最佳治疗方案。免疫检查点抑制剂(ICI)扩大了治疗手段,如今它已成为二线治疗的支柱。同样具有革命性的是美国食品药品监督管理局(FDA)批准了erdafitinib,这是一种强效的成纤维细胞生长因子受体(FGFR)抑制剂,仅用于肿瘤存在特定FGF通路改变的患者。最近,新型化合物抗体药物偶联物(ADC)的引入改善了转移性UC的治疗前景。安罗替尼是一种靶向nectin-4的抗体,nectin-4是一种在UC中高度表达的细胞粘附分子,与单甲基奥瑞他汀E(MMAE)偶联,MMAE是一种微管破坏剂。戈沙妥珠单抗是一种靶向Trop-2的人源化单克隆抗体,Trop-2是一种跨膜糖蛋白,与伊立替康的活性代谢产物偶联。这两种化合物已获得FDA加速批准,用于接受过铂类化疗和免疫治疗的患者。多项正在进行的试验正在研究ICI与化疗、抗血管生成药物或其他ICI联合使用的作用,以及PARP抑制剂和靶向治疗的疗效,希望能为一些重要的未满足需求提供信息。在本综述中,我们旨在评估一线化疗后的当前潜在治疗选择。