The emerging role of immunotherapy in advanced urothelial cancers

被引:9
|
作者
Tabayoyong, William [1 ]
Gao, Jianjun [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
关键词
bladder cancer; immune checkpoint inhibitor; programmed death ligand-1; programmed death 1 receptor; PHASE-II TRIAL; CISPLATIN-INELIGIBLE PATIENTS; 2ND-LINE THERAPY; SINGLE-ARM; ACQUIRED-RESISTANCE; CELL-CARCINOMA; OPEN-LABEL; T-CELLS; PD-1; EXPRESSION;
D O I
10.1097/CCO.0000000000000445
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review 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. Recent findings 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. Summary 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.
引用
收藏
页码:172 / 180
页数:9
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