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外周血中性粒细胞与淋巴细胞比值作为胰腺癌预后标志物及其与肿瘤免疫微环境的关联:一项回顾性队列研究

英文原题:Peripheral blood neutrophil-to-lymphocyte ratio as a prognostic marker and its association with the tumor-immune microenvironment in pancreatic cancer: a retrospective cohort study.

查看英文原题

Peripheral blood neutrophil-to-lymphocyte ratio as a prognostic marker and its association with the tumor-immune microenvironment in pancreatic cancer: a retrospective cohort study.

PubMed 2025/06/25(内容时间) J Gastrointest Oncol Q3 · IF 2.1(JCR 2025)

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研究概要

我们的研究结果表明,高 NLR 值与 PDAC 患者的不良预后密切相关。此外,它与 PDAC 患者 TIME 中肿瘤 CD8+TIL(肿瘤浸润淋巴细胞)和 CD33+细胞的存在显著相关。NLR 可能是一个可用于指导治疗相关决策的生物标志物。

研究思路结论见上方概要

外周血中性粒细胞与淋巴细胞比值(NLR)升高已被报道为包括胰腺导管腺癌(PDAC)在内的多种癌症的不良预后标志物。然而,NLR是否与PDAC的肿瘤免疫微环境(TIME)相关尚不清楚。了解NLR所反映的全身炎症与PDAC中TIME之间的相互作用,对于识别预后生物标志物和潜在治疗靶点至关重要。本研究旨在探讨早期PDAC患者中NLR与临床结局之间的关系以及TIME在PDAC中的影响。

我们进行了一项回顾性分析,包括两个队列:PDAC患者与健康对照,以及未经治疗的I-II期PDAC病例。我们收集了临床数据,包括NLR值,并对PDAC患者进行随访以评估总生存期(OS)和无复发生存期(RFS),同时通过免疫组化染色评估TIME中CD8+ T细胞和CD33+髓源性抑制细胞(MDSCs)。我们进行了统计分析,以评估NLR、临床结局和TIME组分之间的关系,进一步确定NLR在反映TIME状态和预测PDAC患者结局中的价值。

NLR与PDAC患者的OS和RFS呈负相关。此外,NLR被发现是PDAC和早期PDAC的预后因素。NLR与肿瘤内CD8 + T细胞丰度呈负相关(r=-0.345,P=0.004),与CD33 + MDSCs丰度呈正相关(r=0.407,P=0.001)。

展开英文摘要原文

An elevated peripheral blood neutrophil-to-lymphocyte ratio (NLR) has been reported to be a negative prognostic marker in many types of cancer, including pancreatic ductal adenocarcinoma (PDAC). However, whether NLR is associated with the tumor-immune microenvironment (TIME) in PDAC is unclear. Understanding the interplay between systemic inflammation as reflected by NLR and TIME in PDAC is crucial for identifying prognostic biomarkers and potential therapeutic targets. The aim of this study was to examine the relationship between the NLR and clinical outcomes in patients with early-stage PDAC and the impact of the TIME in PDAC.

We conducted a retrospective analysis including two cohorts: PDAC patients versus healthy controls and untreated stage I-II PDAC cases. We collected clinical data, including NLR values and followed PDAC patients for overall survival (OS) and relapse-free survival (RFS), and the TIME was evaluated through immunohistochemical staining for CD8 + T cells and CD33 + myeloid-derived suppressor cells (MDSCs). Statistical analyses were performed to assess the relationship between NLR, clinical outcomes, and TIME components to further determine the value of NLR in reflecting the status of the TIME and predicting outcomes of patients with PDAC.

NLR was negatively associated with OS and RFS in patients with PDAC. Moreover, NLR was found to be a prognostic factor for PDAC and early-stage PDAC. The NLR was inversely correlated with the abundance of tumoral CD8 + T cells (r=-0.345, P=0.004) and positively correlated with that of CD33 + MDSCs (r=0.407, P=0.001).

Our findings indicate that a high NLR value is closely correlated with poor outcomes in patients with PDAC. In addition, it was significantly associated with the presence of tumoral CD8 + tumor-infiltrating lymphocytes and CD33 + cells in the TIME of patients with PDAC. NLR may be a biomarker that can inform treat-related decision-making.

论文信息

作者
Li J、Wang J、Li Y、Jiang W、Zuo D、Zhang X、Xiao J、Inamura K
单位
Department of Clinical Laboratory, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China.China
期刊
Journal of gastrointestinal oncology2025 Jun 30
原文标识
PubMed 40672064 · DOI 10.21037/jgo-2025-283