Tripathi Abhishek, Gupta Shilpa
Section of Hematology Oncology, University of Oklahoma Stephenson Cancer Center, Oklahoma City, OK, USA.
Department of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH, USA.
Asian J Urol. 2020 Jul;7(3):284-290. doi: 10.1016/j.ajur.2020.05.011. Epub 2020 Jun 2.
There has been a significant progress in the treatment of metastatic urothelial carcinoma in the last few years with the advent of immunotherapy after a long gap of no drug approvals for over 4 decades. While immunotherapy with checkpoint inhibitors has revolutionized the treatment of urothelial carcinoma, unfortunately, only a minority of patients respond to immunotherapy. Treatment options for patients who do not respond and/or progress on immunotherapy are very limited and overall prognosis remains dismal in metastatic urothelial carcinoma. The first targeted therapy targeting the fibroblast growth factor receptor (FGFR) was recently approved for bladder cancer, but it is effective only in select patients harboring the FGFR2 and FGFR 3 mutations. Antibody drug conjugates like enfortumab vedotin have shown promising activity in clinical trials. Development of novel targeted therapies remains an area of investigation and an unmet need in bladder cancer. Exploitation of androgen receptor (AR) is a potential strategy for targeted drug development in bladder cancer. A significant proportion of urothelial carcinoma patients express AR irrespective of gender. AR signaling in urothelial carcinoma has been linked to progression through multiple mechanisms, including activation of human epidermal growth factor receptor-2 (EGFR or HER-2) signaling and epithelial to mesenchymal transition (EMT). Furthermore, AR is enriched in the luminal papillary mRNA subtype of urothelial carcinoma and also mediates resistance to cisplatin-based chemotherapy. Preclinical evidence suggests that AR inhibition can successfully inhibit urothelial carcinoma growth as monotherapy and is synergistic with cisplatin-based chemotherapy. We review the preclinical and clinical evidence supporting the putative role of AR signaling in urothelial carcinoma pathogenesis, progression and its role as a novel therapeutic target and future directions.
在过去几十年无药物获批的漫长间隔后,随着免疫疗法的出现,转移性尿路上皮癌的治疗在过去几年取得了显著进展。虽然使用检查点抑制剂的免疫疗法彻底改变了尿路上皮癌的治疗方式,但不幸的是,只有少数患者对免疫疗法有反应。对于那些对免疫疗法无反应和/或病情进展的患者,治疗选择非常有限,转移性尿路上皮癌的总体预后仍然很差。首个靶向成纤维细胞生长因子受体(FGFR)的靶向疗法最近被批准用于膀胱癌,但它仅对携带FGFR2和FGFR 3突变的特定患者有效。像恩杂鲁胺这样的抗体药物偶联物在临床试验中显示出有前景的活性。新型靶向疗法的开发仍然是膀胱癌研究的一个领域和未满足的需求。利用雄激素受体(AR)是膀胱癌靶向药物开发的一种潜在策略。相当一部分尿路上皮癌患者无论性别都表达AR。尿路上皮癌中的AR信号通路通过多种机制与进展相关,包括激活人表皮生长因子受体-2(EGFR或HER-2)信号通路和上皮-间质转化(EMT)。此外,AR在尿路上皮癌的管腔乳头状mRNA亚型中富集,并且还介导对基于顺铂的化疗的耐药性。临床前证据表明,AR抑制作为单一疗法可以成功抑制尿路上皮癌的生长,并且与基于顺铂的化疗具有协同作用。我们综述了支持AR信号通路在尿路上皮癌发病机制、进展中的假定作用及其作为新型治疗靶点的作用和未来方向的临床前和临床证据。