Immune checkpoint inhibitors for metastatic bladder cancer

被引:79
作者
Massari, Francesco [1 ]
Di Nunno, Vincenzo [1 ]
Cubelli, Marta [1 ]
Santoni, Matteo [2 ]
Fiorentino, Michelangelo [3 ]
Montironi, Rodolfo [4 ]
Cheng, Liang [5 ]
Lopez-Beltran, Anto [6 ]
Battelli, Nicola [2 ]
Ardizzoni, Andrea [1 ]
机构
[1] St Orsola Marcello Malpighi Hosp, Div Oncol, Bologna, Italy
[2] Macerata Hosp, Oncol Unit, Macerata, Italy
[3] St Orsola Marcello Malpighi Hosp, Addarii Inst Oncol, Pathol Serv, Bologna, Italy
[4] Polytech Univ Marche Reg, Sch Med, United Hosp, Sect Pathol Anat, Ancona, Italy
[5] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[6] Cordoba Univ, Fac Med, Anat Pathol Unit, Cordoba, Spain
关键词
Urothelial carcinoma; Immune-checkpoint inhibitors; Pembrolizumab; Atezolizumab; Avelumab; Durvalumab; Nivolumab; Ipilimumab; Combination therapy; UROTHELIAL CARCINOMA; PD-1; BLOCKADE; CTLA-4; FUSION PROTEIN; SINGLE-ARM; OPEN-LABEL; CISPLATIN; IMMUNOTHERAPY; NIVOLUMAB; SAFETY;
D O I
10.1016/j.ctrv.2017.12.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy has represented the standard therapy for unresectable or metastatic urothelial carcinoma for more than 20 years. The growing knowledge of the interaction between tumour and immune system has led to the advent of new classes of drugs, the immune-checkpoints inhibitors, which are intended to change the current scenario. To date, immunotherapy is able to improve the overall responses and survival. Moreover, thanks to its safety profile immune-checkpoint inhibitors could be proposed also to patients unfit for standard chemotherapy. No doubts that these agents have started a revolution expected for years, but despite this encouraging results it appears clear that not all subjects respond to these agents and requiring the development of reliable predictive response factors able to isolate patients who can more benefit from these treatments as well as new strategies aimed to improve immunotherapy clinical outcome. In this review we describe the active or ongoing clinical trials involving Programmed Death Ligand 1 (PD-L1), Programmed Death receptor 1 (PD-1) and Cytotoxic-T Lymphocyte Antigen 4 (CTLA 4) inhibitors in urothelial carcinoma focusing our attention on the developing new immune-agents and combination strategies with immune-checkpoint inhibitors. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:11 / 20
页数:10
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