Vlachostergios Panagiotis J, Jakubowski Christopher D, Niaz Muhammad J, Lee Aileen, Thomas Charlene, Hackett Amy L, Patel Priyanka, Rashid Naureen, Tagawa Scott T
Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, NY, USA.
Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
Bladder Cancer. 2018 Jul 30;4(3):247-259. doi: 10.3233/BLC-180169.
Urothelial carcinoma (UC) is characterized by expression of a plethora of cell surface antigens, thus offering opportunities for specific therapeutic targeting with use of antibody-drug conjugates (ADCs). ADCs are structured from two major constituents, a monoclonal antibody (mAb) against a specific target and a cytotoxic drug connected via a linker molecule. Several ADCs are developed against different UC surface markers, but the ones at most advanced stages of development include sacituzumab govitecan (IMMU-132), enfortumab vedotin (ASG-22CE/ASG-22ME), ASG-15ME for advanced UC, and oportuzumab monatox (VB4-845) for early UC. Several new targets are identified and utilized for novel or existing ADC testing. The most promising ones include human epidermal growth factor receptor 2 (HER2) and members of the fibroblast growth factor receptor axis (FGF/FGFR). Positive preclinical and early clinical results are reported in many cases, thus the next step involves further improving efficacy and reducing toxicity as well as testing combination strategies with approved agents.
尿路上皮癌(UC)的特征是表达大量细胞表面抗原,因此为使用抗体药物偶联物(ADC)进行特异性治疗靶向提供了机会。ADC由两个主要成分构成,一种针对特定靶点的单克隆抗体(mAb)和一种通过连接分子连接的细胞毒性药物。已经开发了几种针对不同UC表面标志物的ADC,但处于最先进开发阶段的包括戈沙妥珠单抗(IMMU-132)、恩扎妥昔单抗(ASG-22CE/ASG-22ME)、用于晚期UC的ASG-15ME以及用于早期UC的奥普妥珠单抗(VB4-845)。已经确定了几个新靶点并将其用于新型或现有ADC测试。最有前景的靶点包括人表皮生长因子受体2(HER2)和成纤维细胞生长因子受体轴(FGF/FGFR)的成员。在许多情况下都报告了阳性的临床前和早期临床结果,因此下一步涉及进一步提高疗效、降低毒性以及测试与已获批药物的联合策略。