Towards Next Generation Biomarkers in Natural Killer/T-Cell Lymphoma

被引:5
|
作者
Chan, Jason Yongsheng [1 ,2 ]
Lim, Jing Quan [3 ]
Ong, Choon Kiat [3 ,4 ,5 ]
机构
[1] Natl Canc Ctr Singapore, Div Med Oncol, Singapore 169610, Singapore
[2] SingHlth Duke NUS Blood Canc Ctr, Singapore 169857, Singapore
[3] Natl Canc Ctr Singapore, Div Cellular & Mol Res, Lymphoma Genom Translat Res Lab, Singapore 169610, Singapore
[4] Duke NUS Med Sch, Canc & Stem Cell Biol, Singapore 169857, Singapore
[5] A STAR Agency Sci Technol & Res, Genome Inst Singapore, Singapore 138672, Singapore
来源
LIFE-BASEL | 2021年 / 11卷 / 08期
基金
英国医学研究理事会;
关键词
precision oncology; PD-L1; immunotherapy; prognosis; EBV; BARR-VIRUS-DNA; DEATH-LIGAND; PREDICTS POOR-PROGNOSIS; NASAL-TYPE; EBV-DNA; MACROPHAGES CORRELATE; CD30; EXPRESSION; GENETIC RISK; HIGH NUMBERS; OPEN-LABEL;
D O I
10.3390/life11080838
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Natural killer/T-cell lymphoma (NKTCL) is an Epstein-Barr virus-associated non-Hodgkin lymphoma linked to an aggressive clinical course and poor prognosis. Despite an improvement in survival outcomes with the incorporation of novel agents including immune checkpoint inhibitors in the treatment of NKTCL, a significant proportion of patients still relapse or remain refractory to treatment. Several clinical prognostic models have been developed for NKTCL patients treated in the modern era, though the optimal approach to risk stratification remains to be determined. Novel molecular biomarkers derived from multi-omic profiling have recently been developed, with the potential to improve diagnosis, prognostication and treatment of this disease. Notably, a number of potential biomarkers have emerged from a better understanding of the tumor immune microenvironment and inflammatory responses. This includes a recently described 3 ' UTR structural variant in the PD-L1 gene, which confers susceptibility to checkpoint immunotherapy. In this review, we summarize the biomarker landscape of NKTCL and highlight emerging biomarkers with the potential for clinical implementation.
引用
收藏
页数:13
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