Clinical researches on programmed death-1/programmed death ligand-1 immunity checkpoint inhibitors in solid tumor therapy
Received:June 25, 2017  Revised:July 31, 2017
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DOI:10.11915/j.issn.1671-5403.2017.12.221
Key words:tumor  biomarkers  checkpoint inhibitors  programmed death-1/programmed death ligand-1
Author NameAffiliationE-mail
SUN Peng Department of Oncology, Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China  
XU Yu-Qing Department of Oncology, Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China xuyuqingx@126.com 
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Abstract:
      In recent years, the inhibitors for immunity checkpoint molecules, programmed death-1/programmed death ligand-1 (PD-1/PD-L1), have obtained encouraging results in solid tumor therapy. PD-1, which is mainly expressed in activated T and B cells, plays a vital role in preventing autoimmune and auto-inflammatory reactivity in the normal host. However, PD-1/PD-L1 expres-sion is very high in the tumor microenvironment, which makes T cell activity be suppressed excessively. So tumor cells can escape immune response. PD-L1 expression level may be a predictive biomarker of its antibody treatment effect. Due to responses of long duration and less toxicity, a minority of patients benefit obviously from immunotherapy. In this article, we illuminated the present resear-ches on PD-1/PD-L1 antibody in treatment of malignant melanoma, lung cancer, urothelial carcinoma, renal cell carcinoma, and so on, and also discussed the biomarkers for patient selection.
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