The PD-1 pathway as a therapeutic target to overcome immune escape mechanisms in cancer

被引:34
作者
Henick, Brian S. [1 ]
Herbst, Roy S. [2 ,3 ]
Goldberg, Sarah B. [4 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Yale Comprehens Canc Ctr, Thorac Oncol Res Program, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Yale Comprehens Canc Ctr, Dev Therapeut Program, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Yale Comprehens Canc Ctr, New Haven, CT 06520 USA
关键词
cancer; immunotherapy; programmed death-1; programmed death-ligand 1; T-CELL-ACTIVATION; B7; FAMILY; PROGRAMMED DEATH-1; DILATED CARDIOMYOPATHY; INHIBITORY MOLECULES; ANTI-PD-L1; ANTIBODY; POSITIVE SELECTION; DENDRITIC CELLS; PHASE-III; B7-H1;
D O I
10.1517/14728222.2014.955794
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Immunotherapy is emerging as a powerful approach in cancer treatment. Preclinical data predicted the antineoplastic effects seen in clinical trials of programmed death-1 (PD-1) pathway inhibitors, as well as their observed toxicities. The results of early clinical trials are extraordinarily promising in several cancer types and have shaped the direction of ongoing and future studies. Areas covered: This review describes the biological rationale for targeting the PD-1 pathway with monoclonal antibodies for the treatment of cancer as a context for examining the results of early clinical trials. It also surveys the landscape of ongoing clinical trials and discusses their anticipated strengths and limitations. Expert opinion: PD-1 pathway inhibition represents a new frontier in cancer immunotherapy, which shows clear evidence of activity in various tumor types including NSCLC and melanoma. Ongoing and upcoming trials will examine optimal combinations of these agents, which should further define their role across tumor types. Current limitations include the absence of a reliable companion diagnostic to predict likely responders, as well as lack of data in early-stage cancer when treatment has the potential to increase cure rates.
引用
收藏
页码:1407 / 1420
页数:14
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