Emerging immunotherapies for bladder cancer. Issue 3 (May 2015)

• Record Type: Journal Article
• Authors: Kim, Joseph W.; Tomita, Yusuke; Trepel, Jane; Apolo, Andrea B.
• Is Part Of: Current opinion in oncology. Volume 27:Issue 3(2015:May)
• Publication Date: 2015-05
• Subjects: adoptive T-cell therapy -- B7-H3 -- bladder cancer -- immune escape -- immunotherapy -- NY-ESO-1 -- OX40 -- programmed death-ligand 1 -- urothelial carcinoma; Oncology -- Periodicals; 616.994
• DOI: 10.1097/CCO.0000000000000177
• Languages: English
• ISSNs: 1040-8746

Abstract

Abstract : Purpose of review: Inhibition of immune escape mechanisms, such as the programed death-ligand 1 pathway, has demonstrated rapid, durable responses in multiple tumor types, including advanced urothelial carcinoma. This review discusses emerging immunotherapies for urothelial carcinoma in various stages of clinical development. Recent findings: Urothelial carcinoma has a high mutational burden, which may increase the number of tumor antigens and potentially enhance the ability of the immune system to recognize tumor cells as foreign. However, urothelial carcinoma can evade the immune system by downregulating tumor–antigen presentation, upregulating various immune checkpoints, and inactivating cytotoxic T cells. Immunotherapies for urothelial carcinoma target each of these steps to restore immune-mediated cytotoxicity. Many of these agents are in clinical trials for urothelial carcinoma. Summary: Immunotherapies are active in urothelial carcinoma, but only in a fraction of patients, implying the presence of persistent immune escape. Identifying the mechanisms of immune escape and developing rational combinatorial regimens may make the benefit of immunotherapy accessible to a broader population.