Dynamic versus static biomarkers in cancer immune checkpoint blockade: unravelling complexity

被引:181
作者
Lesterhuis, W. Joost [1 ,2 ]
Bosco, Anthony [3 ]
Millward, Michael J. [1 ,2 ,4 ]
Small, Michael [5 ,6 ]
Nowak, Anna K. [1 ,2 ,4 ]
Lake, Richard A. [1 ,2 ]
机构
[1] Univ Western Australia, Sch Med & Pharmacol, 5th Floor,QQ Block,6 Verdun St, Perth, WA 6009, Australia
[2] Univ Western Australia, Natl Ctr Asbestos Related Dis, 5th Floor,QQ Block,6 Verdun St, Perth, WA 6009, Australia
[3] Univ Western Australia, Telethon Kids Inst, POB 855, Perth, WA, Australia
[4] Sir Charles Gairdner Hosp, Dept Med Oncol, Hosp Ave, Nedlands, WA 6009, Australia
[5] Univ Western Australia, Sch Math & Stat, 35 Stirling Highway, Crawley, WA 6009, Australia
[6] CSIRO, Mineral Resources, 26 Dick Perry Ave, Kensington, WA 6152, Australia
基金
英国医学研究理事会;
关键词
EARLY-WARNING SIGNALS; MYELOID-DERIVED SUPPRESSOR; REGULATORY T-CELLS; PD-1; BLOCKADE; TRANSCRIPTIONAL NETWORK; IMMUNOTHERAPY TARGETS; CRITICAL TRANSITIONS; ANTI-PD-1; ANTIBODY; ANTIGEN-4; NIVOLUMAB;
D O I
10.1038/nrd.2016.233
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
Recently, there has been a coordinated effort from academic institutions and the pharmaceutical industry to identify biomarkers that can predict responses to immune checkpoint blockade in cancer. Several biomarkers have been identified; however, none has reliably predicted response in a sufficiently rigorous manner for routine use. Here, we argue that the therapeutic response to immune checkpoint blockade is a critical state transition of a complex system. Such systems are highly sensitive to initial conditions, and critical transitions are notoriously difficult to predict far in advance. Nevertheless, warning signals can be detected closer to the tipping point. Advances in mathematics and network biology are starting to make it possible to identify such warning signals. We propose that these dynamic biomarkers could prove to be useful in distinguishing responding from non-responding patients, as well as facilitate the identification of new therapeutic targets for combination therapy.
引用
收藏
页码:264 / 272
页数:9
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