New Combination Strategies Using Programmed Cell Death 1/Programmed Cell Death Ligand 1 Checkpoint Inhibitors as a Backbone

被引:37
作者
Hu-Lieskovan, Siwen [1 ]
Ribas, Antoni [1 ]
机构
[1] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol, Jonsson Comprehens Canc Ctr, 11-934 Factor Bldg,10833 Le Conte Ave, Los Angeles, CA 90095 USA
关键词
Adoptive cell transfer; cancer vaccines; combination immunotherapy; checkpoint inhibitor; chemotherapy; epigenetic modification; immune-modulatory agent; oncolytic virus; radiotherapy; tumor microenvironment; RESISTANT PROSTATE-CANCER; COLONY-STIMULATING FACTOR; ANTITUMOR IMMUNE-RESPONSES; LONG-TERM SURVIVAL; REGULATORY T-CELLS; TUMOR-ASSOCIATED MACROPHAGES; COMBINING TARGETED THERAPY; LOCAL RADIATION-THERAPY; TOLL-LIKE RECEPTORS; GROWTH-FACTOR-BETA;
D O I
10.1097/PPO.0000000000000246
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The discovery of immune checkpoints and subsequent clinical development of checkpoint inhibitors have revolutionized the field of oncology. The durability of the antitumor immune responses has raised the hope for long-term patient survival and potential cure; however, currently, only aminority of patients respond. Combination strategies to help increase antigen release and T-cell priming, promote T-cell activation and homing, and improve the tumor immune microenvironment, all guided by predictive biomarkers, can help overcome the tumor immune-evasive mechanisms and maximize efficacy to ultimately benefit the majority of patients. Great challenges remain because of the complex underlying biology, unpredictable toxicity, and accurate assessment of response. Carefully designed clinical trials guided by translational studies of paired biopsies will be key to develop reliable predictive biomarkers to choose which patients would most likely benefit from each strategy.
引用
收藏
页码:10 / 22
页数:13
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