Advanced non-small cell lung cancer: the role of PD-L1 inhibitors
Author(s) -
David F. Heigener,
Martin Reck
Publication year - 2018
Publication title -
journal of thoracic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.682
H-Index - 60
eISSN - 2077-6624
pISSN - 2072-1439
DOI - 10.21037/jtd.2018.01.112
Subject(s) - durvalumab , medicine , atezolizumab , avelumab , tolerability , pd l1 , lung cancer , oncology , chemotherapy , cytotoxicity , pembrolizumab , pharmacology , immunotherapy , cancer , adverse effect , biochemistry , chemistry , in vitro
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 2 nd -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.
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