Li Jing, Wang Jiayi, Li Yuxuan, Jiang Wenna, Zuo Duo, Zhang Xiuse, Xiao Jiawei, Inamura Kentaro, Giovannetti Elisa, Ren Li
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.
Division of Pathology, The Cancer Institute, Japanese Foundation for Cancer Research, Tokyo, Japan.
J Gastrointest Oncol. 2025 Jun 30;16(3):1248-1257. doi: 10.21037/jgo-2025-283. Epub 2025 Jun 25.
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.
据报道,外周血中性粒细胞与淋巴细胞比值(NLR)升高是包括胰腺导管腺癌(PDAC)在内的多种癌症的不良预后标志物。然而,NLR是否与PDAC中的肿瘤免疫微环境(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。本研究的目的是探讨早期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患者进行总生存期(OS)和无复发生存期(RFS)随访,通过对CD8 T细胞和CD33髓源性抑制细胞(MDSC)进行免疫组化染色来评估TIME。进行统计分析以评估NLR、临床结局和TIME成分之间的关系,以进一步确定NLR在反映TIME状态和预测PDAC患者结局方面的价值。
PDAC患者的NLR与OS和RFS呈负相关。此外,发现NLR是PDAC和早期PDAC的预后因素。NLR与肿瘤CD8 T细胞丰度呈负相关(r = -0.345,P = 0.004),与CD33 MDSC丰度呈正相关(r = 0.407,P = 0.001)。
我们的研究结果表明,高NLR值与PDAC患者的不良结局密切相关。此外,它与PDAC患者TIME中肿瘤CD8肿瘤浸润淋巴细胞和CD33细胞的存在显著相关。NLR可能是一种可为治疗相关决策提供依据的生物标志物。