Harnessing the Immune System for the Treatment of Non-Small-Cell Lung Cancer

被引:122
作者
Brahmer, Julie R. [1 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD USA
关键词
BLP25 LIPOSOME VACCINE; PHASE-II; LYMPHOCYTE SUBSETS; BELAGENPUMATUCEL-L; DOUBLE-BLIND; STAGE-IIIB; MELANOMA; ANTIBODY; CHEMOTHERAPY; SAFETY;
D O I
10.1200/JCO.2012.45.8703
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over the last several years, new therapeutic targets have emerged in immunotherapy, particularly the immune checkpoint pathways. Blocking inhibitory pathways via monoclonal antibodies, such as the anti-cytotoxic T-lymphocyte antigen-4 antibody (ipilimumab), anti-programmed cell death-1 antibody (BMS-936558), and anti-programmed cell death-1 ligand antibody (BMS-936559), has the ability to break down the shield that tumors co-opt for their defense. Vaccines are able to help the immune system develop immune memory that can have long-lasting, tumor-specific effects. Newer vaccines, particularly the tumor cell vaccine, belagenpumatucel-L, and the antigen-specific vaccines, melanoma-associated antigen-A3, liposomal BLP-25, TG4010, and recombinant human epidermal growth factor, are being evaluated in some of the largest trials ever attempted in lung cancer therapy. These therapies alone or in combination may hold the key to making immunotherapy a reality in the treatment of lung cancer. J Clin Oncol 31:1021-1028. (C) 2013 by American Society of Clinical Oncology
引用
收藏
页码:1021 / 1028
页数:8
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