| Literature DB >> 29407369 |
Francesco Massari1, Vincenzo Di Nunno2, Marta Cubelli2, Matteo Santoni3, Michelangelo Fiorentino4, Rodolfo Montironi5, Liang Cheng6, Anto Lopez-Beltran7, Nicola Battelli3, Andrea Ardizzoni2.
Abstract
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.Entities:
Keywords: Atezolizumab; Avelumab; Combination therapy; Durvalumab; Immune-checkpoint inhibitors; Ipilimumab; Nivolumab; Pembrolizumab; Urothelial carcinoma
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Year: 2018 PMID: 29407369 DOI: 10.1016/j.ctrv.2017.12.007
Source DB: PubMed Journal: Cancer Treat Rev ISSN: 0305-7372 Impact factor: 12.111