Tumor immune microenvironment in adenoid cystic carcinoma of the lacrimal gland: relationship with histopathology and prognosis.

IF 3.4 2区 医学 Q2 ONCOLOGY
Yi Zhang, Zhipeng Guo, Jie Sun, Yingwen Bi, Rongrong Cai, Rui Zhang, Hui Ren, Jiang Qian, Fengxi Meng
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Abstract

Purpose: To quantitatively investigate the pathological subtypes of lacrimal gland adenoid cystic carcinoma (LGACCs), the tumor immune microenvironment in each pathological subtype, and the relation to survival.

Methods: In this retrospective study, the tumor subtype was determined by H&E staining. Multiplex immunochemistry was performed to define specific immune cells. The tumor immune microenvironment (TIME) was sketched by sequential image scanning and reconstructed by a cytometry platform.

Results: Eighteen patients with adequate paraffin blocks diagnosed with LGACC from 2012 to 2021 were included in this study. Thirteen patients out of the eighteen patients (72.2%)showed a mixture of different pathological subtypes. Each pathological subtype took different percentages on different tumors. The cribriform was the most common subtype, taking an overall percentage of 39%. The rest of the pathological subtypes were tubular (19%), basaloid (17%), cribriform and tubular mixture (C + T) 14%. The sclerosing and comedocarcinomic subtypes were the least seen in LGACC, taking a percentage of 11% altogether. Patients with cribriform dominant component had better overall survival than the non-cribriform dominant patients. Patients with basaloid dominant component had worse clinical outcomes than the non-basaloid dominant ones. The TIME showed high immunogenicity in the tumor margin but declined in the tumor areas. Pathological subtypes rather than individual differences determined the TIME phenotype. The cribriform subtype possessed more immune cell infiltration than other pathological subtypes.

Conclusions: LGACC is composed of multiple pathological subtypes. Each pathological subtype takes different percentages on different tumors, which is related to the prognosis. TIME pattern in LGACC varies among different pathological subtypes, which could indicate novel strategies in immunotherapy.

泪腺腺样囊性癌的肿瘤免疫微环境:与组织病理学和预后的关系。
目的:定量研究泪腺腺样囊性癌(LGACCs)的病理亚型、各病理亚型的肿瘤免疫微环境及其与生存的关系。方法:回顾性研究,采用H&E染色法确定肿瘤亚型。多重免疫化学测定特异性免疫细胞。通过序列图像扫描绘制肿瘤免疫微环境(TIME),并用细胞仪平台重建肿瘤免疫微环境。结果:本研究纳入了2012年至2021年诊断为LGACC的18例石蜡块充足的患者。18例患者中有13例(72.2%)表现为不同病理亚型的混合。每种病理亚型在不同肿瘤中所占比例不同。筛状是最常见的亚型,占总百分比的39%。其余病理亚型为管状(19%)、基底样(17%)、筛状和管状混合型(C + T) 14%。硬化和粉刺癌亚型在LGACC中最少见,总共占11%。筛状显性成分患者的总生存率高于非筛状显性成分患者。基底样蛋白显性成分患者的临床结果较非基底样蛋白显性成分患者差。TIME在肿瘤边缘表现出较高的免疫原性,而在肿瘤区域表现出较低的免疫原性。病理亚型而非个体差异决定了TIME表型。筛状亚型比其他病理亚型具有更多的免疫细胞浸润。结论:LGACC由多种病理亚型组成。每种病理亚型在不同肿瘤中所占比例不同,这与预后有关。不同病理亚型LGACC的时间模式不同,这可能提示免疫治疗的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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