PEMBROLIZUMAB: PD-1 INHIBITION AS A THERAPEUTIC STRATEGY IN CANCER

被引:59
作者
McDermott, J. [1 ]
Jimeno, A. [1 ,2 ]
机构
[1] Univ Colorado, Sch Med, Dept Med, Div Med Oncol, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dev Therapeut Program, Aurora, CO 80045 USA
关键词
MK-3475; Lambrolizumab; Pembrolizumab; Melanoma; NSCLC; anti-pD-1; antibody; T-CELLS; CLINICAL-SIGNIFICANCE; B7-H1; EXPRESSION; TUMOR-CELLS; BLOCKADE; CTLA-4; PHASE; IPILIMUMAB; CARCINOMA; LIGANDS;
D O I
10.1358/dot.2015.51.1.2250387
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Programmed cell death protein 1 (PD-1) and its ligands, programmed cell death 1 ligand 1 (PD-L1) and 2 (PD-L2) play an important role in regulating immune response through various mechanisms. This inhibitory action is thought to assist in immune evasion by cancer cells as PD-1, PD-L1 and PD-L2 have been found to be abnormally expressed by tumor cells and lymphocytes in the tumor microenvironment. Preclinical studies described PD-1 blockade resulting in tumor growth suppression and even decreased metastasis. This has led to the development of pembrolizumab (MK-3475), a highly selective, humanized monoclonal IgG(4) -kappa isotype antibody against PD-1. Early clinical trials have shown high tumor response rates and long duration of effect in previously treated advanced melanoma resulting in accelerated FDA approval for the drug in this situation. Pembrolizumab has also had success in non-small cell lung cancer and is being tested in multiple other tumor types. This review will discuss the development, preclinical data, pharmacokinetics and clinical efficacy to date of pembrolizumab.
引用
收藏
页码:7 / 20
页数:14
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