| Literature DB >> 29296516 |
Vito Vanella1, Lucia Festino1, Martina Strudel1, Ester Simeone1, Antonio M Grimaldi1, Paolo A Ascierto1.
Abstract
Checkpoint inhibitors have improved survival for patients with melanoma, non-small-cell lung cancer (NSCLC), bladder, head and neck and other cancers. Antibodies against PD-L1, including atezolizumab, avelumab and durvalumab, are also being developed and have been approved for various cancers. Compared with anti-CTLA-4 drugs, studies with anti-PD-1/PD-L1 agents have suggested higher response rates and improved survival. Targeting PD-L1 rather than PD-1 may also theoretically offer further benefit, with the potential for improved efficacy and reduced toxicity, although this has not been clearly shown by clinical experience to date. Anti-PD-L1 agents have shown good efficacy and manageable toxicity in several tumor types.Entities:
Keywords: Atezolizumab; Merkel cell carcinoma; PD-L1; avelumab; bladder cancer; durvalumab; immunotherapy; lung cancer; melanoma
Year: 2017 PMID: 29296516 PMCID: PMC5739559 DOI: 10.1080/2162402X.2017.1365209
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110