Immunogenetic variations predict immune-related adverse events for PD-1/PD-L1 inhibitors

被引:11
|
作者
Xin, Zhaodan [1 ]
You, Liting [1 ,2 ]
Na, Feifei [3 ]
Li, Jin [1 ]
Chen, Min [4 ]
Song, Jiajia [1 ]
Bai, Ling [1 ]
Chen, Jie [1 ]
Zhou, Juan [1 ]
Ying, Binwu [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Lab Med, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Natl Clin Res Ctr Geriatr, Lab Aging Res & Canc Drug Target,State Key Lab Bio, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Thorac Canc, Chengdu 610041, Peoples R China
[4] Hainan Med Coll, Affiliated Hosp 1, Dept Lab Med, Haikou 570100, Hainan, Peoples R China
基金
中国国家自然科学基金;
关键词
Immune checkpoint inhibitors; PD-1; PD-L1; inhibitors; Immune-related adverse events; Therapeutic biomarker; GENOME-WIDE ASSOCIATION; RHEUMATOID-ARTHRITIS; POOLED ANALYSIS; RISK; SUSCEPTIBILITY; VARIANTS; DISEASES; PATHWAY; CD45;
D O I
10.1016/j.ejca.2023.01.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: PD-1/PD-L1 inhibitors have brought remarkable benefits but can cause profound immune-related adverse events (irAEs). The host immunogenetic background is likely to play a role in irAE susceptibility. In this study, we aimed to identify potential im-munogenetic biomarkers to predict irAEs. Methods: Patients with solid tumours receiving PD-1/PD-L1 blockade were recruited and fol-lowed up. Genes considered pivotal contributors to tumour-immunity and autoimmune dis-eases were screened out via protein-protein interaction network and Cytoscape. Consequently, thirty-nine variants in eighteen genes were genotyped using the multiplex gen-otyping assay. Association analysis between genetic variants and irAEs as well as irAEs-free survival was performed. Results: Four immunogenetic variants as predictive biomarkers of irAEs were identified. The C allele of Mitogen-Activated Protein Kinase 1 (MAPK1) rs3810610 (odds ratio [OR] = 1.495, 95% confidence interval [CI] = 1.093-2.044, P = 0.012) was a risk predictor while the A allele of PTPRC rs6428474 (OR = 0.717, 95% CI = 0.521-0.987, P = 0.041) was a protective factor for all-grade irAEs. The A allele of ADAD1 rs17388568 (OR = 2.599, 95% CI = 1.355-4.9 83, P = 0.003) increased the risk while the G allele of IL6 rs1800796 (OR = 0.425, 95% CI = 0.205-0.881, P = 0.018) protected patients from high-grade irAEs. Significant immunogenetic variants reached a similar tendency in PD-1 blockade or lung can- cer subgroups. In multivariate Cox regression analysis, the MAPK1 rs3810610 was an inde- pendent factor regarding all-grade irAEs-free survival (CC versus CT or TT: hazard ratio [HR] = 0.71, 95% CI = 0.52-0.99, P = 0.042). ADAD1 rs17388568 (AA versus AG or GG: HR = 0.11, 95% CI = 0.025-0.49, P = 0.004) and IL6 rs1800796 (GG or GC versus CC: HR = 3.10, 95% CI = 1.315-7.29, P = 0.01) were independent variables for high-grade irAEs-free survival. Conclusion: We first identified several immunogenetic polymorphisms associated with irAEs and irAEs-free survival in PD-1/PD-L1 blockade-treated tumour patients, and they may serve as potential predictive biomarkers. 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:124 / 136
页数:13
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