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.
Keywords
- PD-L1 inhibition
- atezolizumab
- avelumab
- durvalumab
- non-small cell lung cancer (NSCLC)
- BMS, MSD, Pfizer, Lilly, Astra Zeneca, Chugai, Fresenius
- Honoraria for Speeches:
- Boehringer Ingelheim, Roche, BMS, MSD, Pfizer, Lilly, Astra Zeneca
- Travel
- Reimbursement: Boehringer Ingelheim, Roche, BMS, MSD, Pfizer, Lilly, AstraZeneca,
- Chugai, Fresenius. M Reck: Advisory Board: Boehringer Ingelheim, Roche, BMS, MSD,
- Pfizer, Lilly, Astra Zeneca, Chugai
- Honoraria for Speeches: Boehringer
- Ingelheim, Roche, BMS, MSD, Pfizer, Lilly, AstraZeneca
- Travel Reimbursement:
- Boehringer Ingelheim, Roche, BMS, MSD, Pfizer, Lilly, Astra Zeneca, Chugai,
- Fresenius.