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头颈部鳞状细胞癌免疫治疗反应的诊断预测指标

Diagnostic Predictors of Immunotherapy Response in Head and Neck Squamous Cell Carcinoma.

作者信息

Meliante Piero Giuseppe, Zoccali Federica, de Vincentiis Marco, Ralli Massimo, Petrella Carla, Fiore Marco, Minni Antonio, Barbato Christian

机构信息

Department of Sense Organs, Sapienza University of Rome, 00161 Roma, Italy.

Institute of Biochemistry and Cell Biology (IBBC), National Research Council (CNR), Department of Sense Organs, Sapienza University of Rome, Viale del Policlinico 155, 00161 Roma, Italy.

出版信息

Diagnostics (Basel). 2023 Feb 23;13(5):862. doi: 10.3390/diagnostics13050862.

Abstract

Programmed cell death ligand-1 (PD-L1) binds PD-1 on CD lymphocytes, inhibiting their cytotoxic action. Its aberrant expression by head and neck squamous cell carcinoma (HNSCC) cells leads to immune escape. Pembrolizumab and nivolumab, two humanized monoclonal antibodies against PD-1, have been approved in HNSCC treatment, but ~60% of patients with recurrent or metastatic HNSCC fail to respond to immunotherapy and only 20 to 30% of treated patients have long-term benefits. The purpose of this review is to analyze all the fragmentary evidence present in the literature to identify what future diagnostic markers could be useful for predicting, together with PD-L1 CPS, the response to immunotherapy and its durability. We searched PubMed, Embase, and the Cochrane Register of Controlled Trials and we summarize the evidence collected in this review. We confirmed that PD-L1 CPS is a predictor of response to immunotherapy, but it should be measured across multiple biopsies and repeatedly over time. PD-L2, IFN-γ, EGFR, VEGF, TGF-β, TMB, blood TMB, CD73, TILs, alternative splicing, tumor microenvironment, and some macroscopic and radiological features are promising predictors worthy of further studies. Studies comparing predictors appear to give greater potency to TMB and CXCR9.

摘要

程序性细胞死亡配体1(PD-L1)与CD淋巴细胞上的PD-1结合,抑制其细胞毒性作用。头颈部鳞状细胞癌(HNSCC)细胞中PD-L1的异常表达导致免疫逃逸。帕博利珠单抗和纳武利尤单抗这两种抗PD-1人源化单克隆抗体已被批准用于HNSCC治疗,但约60%的复发性或转移性HNSCC患者对免疫治疗无反应,只有20%至30%的接受治疗患者有长期获益。本综述的目的是分析文献中所有零散证据,以确定哪些未来诊断标志物可与PD-L1联合阳性评分(CPS)一起用于预测免疫治疗反应及其持久性。我们检索了PubMed、Embase和Cochrane对照试验注册库,并总结了本综述中收集的证据。我们证实PD-L1 CPS是免疫治疗反应的预测指标,但应在多次活检中进行测量,并随时间重复测量。PD-L2、干扰素-γ(IFN-γ)、表皮生长因子受体(EGFR)、血管内皮生长因子(VEGF)、转化生长因子-β(TGF-β)、肿瘤突变负荷(TMB)、血液TMB、CD73、肿瘤浸润淋巴细胞(TILs)、可变剪接、肿瘤微环境以及一些宏观和放射学特征都是值得进一步研究的有前景的预测指标。比较各预测指标的研究似乎显示肿瘤突变负荷和CXC趋化因子受体9(CXCR9)更具预测效力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e60/10001329/9f58f4944b0c/diagnostics-13-00862-g001.jpg

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