| Literature DB >> 29951298 |
David F Heigener1,2, Martin Reck1,3.
Abstract
PD-L1 and PD-1 inhibitors were both developed to combat a huge array of cancers. Both classes of agents block the PD-1/PD-L1 pathway. Unlike PD-1 inhibitors, PD-L1 inhibitors do also block the B-7.1-receptor and leave the PD-L2/PD-1 axis unaffected. Whether these differences enhance efficacy and tolerability is not clear yet. There are three PD-L1 inhibitors approved or in late clinical development: Atezolizumab, approved in 2nd-line treatment of non-small cell lung cancer, durvalumab, showing promising results as a consolidation therapy in stage III disease and avelumab, the only drug exploiting antigen-dependent cytotoxicity. Future directions are the combination of these compounds with chemotherapy or other immuno-oncologic drugs.Entities:
Keywords: PD-L1 inhibition; atezolizumab; avelumab; durvalumab; non-small cell lung cancer (NSCLC)
Year: 2018 PMID: 29951298 PMCID: PMC5994502 DOI: 10.21037/jtd.2018.01.112
Source DB: PubMed Journal: J Thorac Dis ISSN: 2072-1439 Impact factor: 2.895