Wenqian Chen, Andrea S Fung, John B McIntyre, Roderick Simpson, Arfan R Afzal, Desiree Hao, Harold Lau
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引用次数: 10
摘要
目的:尽管缺乏免疫微环境的信息,但免疫检查点抑制剂在腺样囊性癌(ACC)中的作用的早期临床研究正在进行中。本研究旨在更好地表征ACC肿瘤的免疫微环境,并基于肿瘤浸润淋巴细胞(TIL)和程序性死亡配体1 (PD-L1)的表达来评估生存结果。方法:收集24例ACC患者的患者特征、治疗及转归资料。免疫组化法定量CD8+(cluster of differentiation 8) TIL和PD-L1表达。用Kaplan-Meier分析评估标志物表达和生存结果。结果:所有病例PD-L1表达均为阴性;TIL高表达4例,中度表达8例,低表达12例。基于TIL的表达,无病生存期和总生存期没有差异。结论:腺样囊性癌与免疫原性微环境差有关,PD-L1表达缺失,CD8+ TILs低。TIL表达与生存无相关性。这些数据表明,PD-L1和TIL表达不太可能作为免疫治疗反应的预测性生物标志物。
Assessment Of Tumour Infiltrating Lymphocytes And Pd-l1 Expression In Adenoid Cystic Carcinoma Of The Salivary Gland.
Purpose: Early phase clinical studies are ongoing to evaluate the role of immune checkpoint inhibitors in adenoid cystic carcinoma (ACC) despite a paucity of information on the immune microenvironment. This study aims to better characterize the immune microenvironment of ACC tumours and evaluate survival outcomes based on tumour infiltrating lymphocyte (TIL) and programmed death-ligand 1 (PD-L1) expression.
Methods: Patient characteristics, treatment and outcome data were collected for 24 ACC patients. The CD8+(cluster of differentiation 8) TIL and PD-L1 expression were quantified by immunohistochemistry. Marker expression and survival outcomes were evaluated by Kaplan-Meier analysis.
Results: All cases were negative for PD-L1 expression; four cases had focal high, eight cases had focal moderate and 12 cases had low TIL expression. Based on TIL expression, there was no difference in disease-free or overall survival.
Conclusion: Adenoid cystic carcinoma tumours were found to be associated with a poor immunogenic microenvironment, with absent PD-L1 expression and low CD8+ TILs. There was no association between TIL expression and survival. These data suggest that PD-L1 and TIL expression are unlikely to be useful as predictive biomarkers for response to immunotherapy.
期刊介绍:
Clinical and Investigative Medicine (CIM), publishes original work in the field of Clinical Investigation. Original work includes clinical or laboratory investigations and clinical reports. Reviews include information for Continuing Medical Education (CME), narrative review articles, systematic reviews, and meta-analyses.