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联合免疫评分用于早期非小细胞肺癌的预后分层

Combined Immunoscore for Prognostic Stratification of Early Stage Non-Small-Cell Lung Cancer.

作者信息

Boscolo Alice, Fortarezza Francesco, Lunardi Francesca, Comacchio Giovanni, Urso Loredana, Frega Stefano, Menis Jessica, Bonanno Laura, Guarneri Valentina, Rea Federico, Conte PierFranco, Calabrese Fiorella, Pasello Giulia

机构信息

Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.

Pathology Unit, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Padua, Italy.

出版信息

Front Oncol. 2020 Sep 25;10:564915. doi: 10.3389/fonc.2020.564915. eCollection 2020.

Abstract

BACKGROUND

To date, no combined immunoscore has been evaluated for prognostic stratification of early stage non-small-cell lung cancer (NSCLC). The main goal of this study was to investigate the prognostic impact of programmed death ligand 1 (PD-L1) expression and different immune cell components (CD4+, CD8+ T-lymphocytes, and CD68+ macrophages) in early stage NSCLC patients, distinguishing peritumoral (PT) and intratumoral (IT) localizations. The secondary aim was to identify a combined immunoscore to optimize the prognostic stratification of NSCLC patients.

METHODS

This retrospective study included surgical specimens from consecutive chemo-naive stage II-III radically resected NSCLC patients. Immunohistochemistry was carried out to evaluate PD-L1 expression and to quantify IT and PT CD4+, CD8+ T-lymphocytes, and CD68+ macrophages. The impact of a single marker and of a combination of multiple markers on overall survival (OS) was investigated.

RESULTS

Seventy-nine patients were included in the study. PD-L1 expression was associated with worse prognosis (3 years OS: 58% in high- compared with 67% in low-expressing tumors), even though without statistical significance. When integrating PT CD8+, CD4+, and CD68 into a combined PT immunoscore, a significant prognostic stratification of patients was obtained and confirmed at multivariate analysis (3 years OS: 86% in patients with low PT immunoscore vs. 59% in patients with high PT immunoscore, = 0.018). The integration of derived neutrophil/lymphocyte ratio (dNLR) with combined PT immunoscore improved prognostic stratification, with longer OS in patients with low PT immunoscore and low dNLR ( = 0.002).

CONCLUSION

The combined PT immunoscore (CD8+, CD4+, and CD68) integrated with dNLR may be a promising marker for the development of an integrated Tumor, Node, Metastasis (TNM) immunoscore.

摘要

背景

迄今为止,尚未对联合免疫评分用于早期非小细胞肺癌(NSCLC)的预后分层进行评估。本研究的主要目的是调查程序性死亡配体1(PD-L1)表达以及不同免疫细胞成分(CD4 +、CD8 + T淋巴细胞和CD68 +巨噬细胞)在早期NSCLC患者中的预后影响,区分瘤旁(PT)和瘤内(IT)定位。次要目的是确定一种联合免疫评分,以优化NSCLC患者的预后分层。

方法

这项回顾性研究纳入了连续的未经化疗的II-III期接受根治性切除的NSCLC患者的手术标本。进行免疫组织化学以评估PD-L1表达,并对IT和PT的CD4 +、CD8 + T淋巴细胞和CD68 +巨噬细胞进行定量。研究了单一标志物和多种标志物组合对总生存期(OS)的影响。

结果

79例患者纳入研究。PD-L1表达与较差的预后相关(3年总生存率:高表达肿瘤为58%,低表达肿瘤为67%),尽管无统计学意义。将PT CD8 +、CD4 +和CD68整合为联合PT免疫评分时,患者获得了显著的预后分层,并在多变量分析中得到证实(3年总生存率:PT免疫评分低的患者为86%,PT免疫评分高的患者为59%,P = 0.018)。将衍生的中性粒细胞/淋巴细胞比值(dNLR)与联合PT免疫评分相结合可改善预后分层,PT免疫评分低且dNLR低的患者总生存期更长(P = 0.002)。

结论

联合PT免疫评分(CD8 +、CD4 +和CD68)与dNLR相结合可能是开发综合肿瘤、淋巴结、转移(TNM)免疫评分的一个有前景的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fba2/7544833/f422a514dcf8/fonc-10-564915-g001.jpg

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