Gene-expression profiling to predict responsiveness to immunotherapy

被引:64
|
作者
Jamieson, N. B. [1 ,2 ,3 ]
Maker, A. V. [4 ,5 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Sch Med, Inst Canc Sci,Wolfson Wohl Canc Res Ctr, Glasgow, Lanark, Scotland
[2] Univ Glasgow, Coll Med Vet & Life Sci, Sch Med, Acad Surg Unit, Glasgow, Lanark, Scotland
[3] Glasgow Royal Infirm, West Scotland Pancreat Unit, Glasgow, Lanark, Scotland
[4] Univ Illinois, Dept Surg, Div Surg Oncol, Chicago, IL 60680 USA
[5] Univ Illinois, Dept Microbiol & Immunol, Chicago, IL 60680 USA
关键词
PD-1; BLOCKADE; MUTATIONAL PROCESSES; CTLA-4; IMMUNE CELLS; PHASE-III; CANCER; IPILIMUMAB; SURVIVAL; RESISTANCE; NIVOLUMAB;
D O I
10.1038/cgt.2016.63
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recent clinical successes with immunotherapy have resulted in expanding indications for cancer therapy. To enhance antitumor immune responses, and to better choose specific strategies matched to patient and tumor characteristics, genomic-driven precision immunotherapy will be necessary. Herein, we explore the role that tumor gene-expression profiling (GEP) may have in the prediction of immunotherapeutic response: Genetic markers associated with response to immunotherapy are addressed as they pertain to the tumor genomic landscape, the extent of DNA damage, tumor mutational load and tumor-specific neoantigens. Furthermore, genetic markers associated with resistance to checkpoint blockade and relapse are reviewed. Finally, the utility of GEP to identify new tumor types for immunotherapy and implications for combinatorial strategies are summarized.
引用
收藏
页码:134 / 140
页数:7
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