Molecular Pathways: Next-Generation Immunotherapy-Inhibiting Programmed Death-Ligand 1 and Programmed Death-1

被引:495
作者
Chen, Daniel S. [2 ,3 ]
Irving, Bryan A. [3 ]
Hodi, F. Stephen [1 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Stanford Med Oncol, Stanford, CA USA
[3] Genentech Inc, San Francisco, CA 94080 USA
关键词
ENDOTHELIAL GROWTH-FACTOR; B7-H1; PD-L1; T-CELLS; CLINICAL-SIGNIFICANCE; POTENTIAL MECHANISM; POOR-PROGNOSIS; PHASE-I; EXPRESSION; CARCINOMA; RECEPTOR;
D O I
10.1158/1078-0432.CCR-12-1362
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of T-cell-based immune therapy for cancer has been to generate durable clinical benefit for patients. Following a generation of therapies that largely showed minimal activity, substantial toxicity, and no biomarkers to identify which patients benefit from treatment, early studies are showing signs that programmed death-ligand 1 (PD-L1) and programmed death-1 (PD-1) inhibitors are highly active. Preclinical and early data from clinical studies suggest that targeting this pathway can induce durable clinical responses in patients in a variety of tumor types, including lung and colon cancer. Furthermore, correlations with tumor PD-L1 expression may enable selection of patients most likely to benefit from treatment. The emerging data not only offer the hope of better cancer therapy but also provide evidence that changes our understanding of how the host immune system interacts with human cancer. Clin Cancer Res; 18(24); 6580-7. (C)2012 AACR.
引用
收藏
页码:6580 / 6587
页数:8
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