Narrative review of the prognostic significance of immune cells in the tumor microenvironment of stage I lung cancer

Ogheneyoma Akpoviroro, Kei Suzuki
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引用次数: 2

Abstract

: Current staging for lung cancer is primarily based on TNM staging, which is purely anatomical. This staging method has served an important purpose of stratifying patients into risk categories based on tumor physical characteristics including tumor size, nodal involvement and metastasis. Nonetheless, the TNM staging has its limitations. One such limitation is the fact that this staging method cannot prognostically discriminate within the same tumor stage. This issue may become relevant with the increasing number of stage I patients being detected as a result of lung cancer screening. As such, investigations for additional prognostic markers become important. The tumor immune microenvironment (IME), including infiltrating immune cells, cell surface markers of these infiltrating cells and of the tumor cells, and signaling proteins (specifically cytokines), could provide the opportunity to stratify patients with early-stage lung cancer based on prognosis (e.g., post-operative recurrence risk) and provide insight on therapeutic responses as well as therapeutic targets. Knowledge of the IME in cancers is important as it serves as a basis for research that attempts to study the possibility of employing the immune system to actively destroy cancer cells (i.e., cancer immunotherapy). This article aims to review recent findings as they relate to prognosticators in the IME of stage I lung cancer. 17 , a cell infiltration, OS, I–II CD8+ infiltration a cell showed a positive correlation with increased CD8+ infiltration in univariate (P=0.002, 95% CI: 0.217–0.714, HR: 0.393) and multivariate analyses (P=0.034, 95% CI: 0.053– 0.892. HR: 0.218). Similar findings were shown for OS in univariate analysis (P=0.044, 95% CI: 0.259–0.982, HR: multivariate analysis showed a trend between high CD8+ TILs and improved OS (P=0.070, 95% CI: 0.276–1.052, HR: 0.539) et the of cells in NSCLC
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免疫细胞在I期肺癌肿瘤微环境中的预后意义
目前肺癌的分期主要基于TNM分期,这是纯粹的解剖学分期。这种分期方法的重要目的是根据肿瘤的物理特征(包括肿瘤大小、淋巴结受累情况和转移情况)将患者划分为不同的风险类别。尽管如此,TNM分期有其局限性。这样的一个限制是,这种分期方法不能在同一肿瘤分期内进行预后区分。这个问题可能与越来越多的I期患者因肺癌筛查而被发现有关。因此,对其他预后指标的调查变得很重要。肿瘤免疫微环境(IME),包括浸润性免疫细胞、浸润性细胞和肿瘤细胞的细胞表面标记物以及信号蛋白(特别是细胞因子),可以根据预后(如术后复发风险)对早期肺癌患者进行分层,并提供治疗反应和治疗靶点的见解。了解癌症中的IME是很重要的,因为它是试图研究利用免疫系统主动摧毁癌细胞(即癌症免疫治疗)的可能性的基础。这篇文章的目的是回顾最近的发现,因为他们在I期肺癌的IME预测。17、在单因素分析(P=0.002, 95% CI: 0.217-0.714, HR: 0.393)和多因素分析(P=0.034, 95% CI: 0.053 - 0.892)中,细胞浸润、OS、I-II CD8+浸润与细胞CD8+浸润增加呈正相关。人力资源:0.218)。多因素分析显示,高CD8+ TILs与非小细胞肺癌细胞的OS (P=0.044, 95% CI: 0.259 ~ 0.982, HR: 0.539)之间存在相关性(P=0.070, 95% CI: 0.275 ~ 1.052, HR: 0.539)
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