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评估唾液腺癌腺样囊性癌中的肿瘤浸润淋巴细胞和 PD-L1 表达。

Assessment Of Tumour Infiltrating Lymphocytes And Pd-l1 Expression In Adenoid Cystic Carcinoma Of The Salivary Gland.

机构信息

Department of Pathology and Laboratory Medicine, University of Calgary, Alberta, Canada.

Department of Oncology, Queen's University, Kingston, Ontario, Canada.

出版信息

Clin Invest Med. 2021 Mar 21;44(1):E38-41. doi: 10.25011/cim.v44i1.35218.

Abstract

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.

摘要

目的

尽管关于腺样囊性癌 (ACC) 的免疫微环境的信息有限,但仍有许多正在进行的早期临床研究来评估免疫检查点抑制剂的作用。本研究旨在更好地描述 ACC 肿瘤的免疫微环境,并根据肿瘤浸润淋巴细胞 (TIL) 和程序性死亡配体 1 (PD-L1) 表达来评估生存结果。

方法

收集了 24 例 ACC 患者的患者特征、治疗和预后数据。采用免疫组织化学法检测 CD8+(分化簇 8)TIL 和 PD-L1 的表达。通过 Kaplan-Meier 分析评估标志物表达和生存结果。

结果

所有病例均无 PD-L1 表达;4 例有局灶性高表达,8 例有局灶性中度表达,12 例有低 TIL 表达。根据 TIL 表达,无疾病进展或总生存率的差异。

结论

发现腺样囊性癌肿瘤与免疫原性差的微环境相关,无 PD-L1 表达和低 CD8+TIL。TIL 表达与生存之间没有关联。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生物标志物。

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