PD-L1 inhibitors in the pipeline: Promise and progress

被引:38
|
作者
Vanella, Vito [1 ]
Festino, Lucia [1 ]
Strudel, Martina [1 ]
Simeone, Ester [1 ]
Grimaldi, Antonio M. [1 ]
Ascierto, Paolo A. [1 ]
机构
[1] Ist Nazl Tumori, Melanoma Canc Immunotherapy & Innovat Therapies U, Fdn G Pascale, Naples, Italy
来源
ONCOIMMUNOLOGY | 2018年 / 7卷 / 01期
关键词
Atezolizumab; avelumab; bladder cancer; durvalumab; immunotherapy; lung cancer; melanoma; Merkel cell carcinoma; PD-L1; METASTATIC UROTHELIAL CARCINOMA; DEATH-LIGAND; ANTI-PD-L1; ANTIBODY; OPEN-LABEL; CLINICAL ACTIVITY; ADVERSE EVENTS; CELL-CARCINOMA; CANCER; MULTICENTER; IPILIMUMAB;
D O I
10.1080/2162402X.2017.1365209
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1 / 11
页数:11
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