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

被引:10
作者
Meliante, Piero Giuseppe [1 ]
Zoccali, Federica [1 ]
de Vincentiis, Marco [1 ]
Ralli, Massimo [1 ]
Petrella, Carla [2 ]
Fiore, Marco [2 ]
Minni, Antonio [1 ,3 ]
Barbato, Christian [2 ]
机构
[1] Sapienza Univ Rome, Dept Sense Organs, I-00161 Rome, Italy
[2] Sapienza Univ Rome, Inst Biochem & Cell Biol IBBC, Natl Res Council CNR, Dept Sense Organs, Viale Policlin 155, I-00161 Rome, Italy
[3] ASL Rieti Sapienza Univ, Osped San Camillo Lellis, Div Otolaryngol Head & Neck Surg, Viale Kennedy, I-02100 Rieti, Italy
关键词
head and neck squamous cell carcinoma; immunotherapy; PD-1/PD-L1; immunotherapy molecular marker; immunotherapy resistance; pembrolizumab; nivolumab; chemotherapy; PROGRAMMED DEATH LIGAND-1; IFN-GAMMA; PD-L1; EXPRESSION; SIGNALING PATHWAYS; CANCER-IMMUNITY; OPEN-LABEL; TUMOR; B7-H1; CHEMOTHERAPY; RECURRENT;
D O I
10.3390/diagnostics13050862
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Programmed cell death ligand-1 (PD-L1) binds PD-1 on CD8+ 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 similar to 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-gamma, EGFR, VEGF, TGF-beta, 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.
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页数:14
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