The University of Texas MD Anderson Cancer Center, Department of Urology.
The University of Texas MD Anderson Cancer Center, Department of Genitourinary Medical Oncology, Houston, Texas, USA.
Curr Opin Oncol. 2018 May;30(3):172-180. doi: 10.1097/CCO.0000000000000445.
Recent Food and Drug Administration (FDA) approval of five new immune checkpoint inhibitors for the treatment of metastatic urothelial cancer represents the first major treatment breakthrough for this disease since the introduction of combination chemotherapy over 30 years ago. This review examines the recent clinical trials leading to FDA approval of these agents, the current challenges facing immunotherapy and areas that require further research.
The programmed death 1 receptor (PD-1) and its ligand programmed death ligand-1 (PD-L1) are important negative regulators of immune activity, preventing destruction of normal tissues and autoimmunity. Aggressive bladder cancer cells express aberrantly high levels of PD-L1, hijacking the normal immune-regulatory pathway to evade detection and destruction by the immune system. Blockade of the PD-1/PD-L1 axis with immune checkpoint inhibitors augments the immune system's ability to eradicate bladder cancer with impressive safety and tolerability profiles.
Recent clinical trials demonstrate that patients with metastatic urothelial carcinoma are responsive to immune checkpoint inhibitor therapy. Optimal treatment regimens are still under development, but activity has been demonstrated in both the first and second-line setting for metastatic disease.
最近食品和药物管理局(FDA)批准了五种新的免疫检查点抑制剂用于治疗转移性尿路上皮癌,这是 30 多年前联合化疗以来该疾病治疗的首次重大突破。这篇综述检查了导致这些药物获得 FDA 批准的最近临床试验,免疫疗法面临的当前挑战和需要进一步研究的领域。
程序性死亡受体 1(PD-1)及其配体程序性死亡配体-1(PD-L1)是免疫活性的重要负调节剂,可防止正常组织的破坏和自身免疫。侵袭性膀胱癌细胞异常高表达 PD-L1,劫持正常的免疫调节途径,逃避免疫系统的检测和破坏。用免疫检查点抑制剂阻断 PD-1/PD-L1 轴增强了免疫系统消除膀胱癌的能力,具有令人印象深刻的安全性和耐受性。
最近的临床试验表明,转移性尿路上皮癌患者对免疫检查点抑制剂治疗有反应。最佳治疗方案仍在开发中,但在转移性疾病的一线和二线治疗中均显示出活性。