Gao Kun, Wei Zhigong, Liu Zheran, Pei Yiyan, Li Huilin, Song Ge, Xiang Jin, Ge Junyou, Qing Yan, Wei Youneng, Ai Ping, Chen Ye, Peng Xingchen
Division of Head & Neck Tumor Multimodality Treatment, Department of Radiation Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Department of Targeting Therapy & Immunology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Head Neck. 2025 Jul;47(7):1928-1938. doi: 10.1002/hed.28101. Epub 2025 Feb 12.
Neutrophil-to-lymphocyte ratio (NLR) can be treated as a simple indicator of patients' immune status by representing the state of the systemic inflammatory response. Immunotherapy now is the accepted second-line treatment for recurrent or metastatic nasopharyngeal carcinoma (R/M NPC). However, the significance of NLR in patients with R/M NPC undergoing treatment with PD-L1 (programmed cell death-ligand 1) inhibitors is still uncertain.
We analyzed the relationship between baseline NLR with 153 patients' efficacy and survival from a multicenter, prospective, Phase 2 study. We employed restricted cubic spline plots to get the nonlinear relationship between NLR and progression-free survival (PFS) or overall survival (OS). We identified the ideal cut-off value through the analysis of the receiver operating characteristic curve (ROC curve). We used Logistic regression, Cox regression, Log-rank test, and Kaplan-Meier method to analyze the association between NLR and patients' disease control rate (DCR) and PFS or OS.
The ideal threshold value for NLR was 2.826. NLR was identified as a significant independent predictor of DCR (OR = 0.17, 95% CI = 0.05-0.48, p = 0.001), indicating that a higher NLR is associated with worse DCR. NLR (AUC = 0.634) showed superior predictive capability for DCR in comparison to lymphocytes (AUC = 0.602) and neutrophils (AUC = 0.593). High NLR values were risk factors both for poor PFS (HR = 2.53, 95% CI = 1.58-4.06, p < 0.001) and OS (HR = 3.89, 95% CI = 2.09-7.24, p < 0.001).
Elevated NLR is strongly associated with lower response to treatment and reduced survival rates in patients with R/M NPC being treated with PD-L1 inhibitors. Patients with high NLR values have poor efficacy and survival.
中性粒细胞与淋巴细胞比值(NLR)可作为反映全身炎症反应状态的指标,用于评估患者的免疫状态。免疫疗法目前是复发或转移性鼻咽癌(R/M NPC)公认的二线治疗方法。然而,NLR在接受程序性死亡配体1(PD-L1)抑制剂治疗的R/M NPC患者中的意义仍不明确。
我们分析了一项多中心、前瞻性II期研究中153例患者的基线NLR与疗效及生存之间的关系。我们采用限制立方样条图来获取NLR与无进展生存期(PFS)或总生存期(OS)之间的非线性关系。通过分析受试者工作特征曲线(ROC曲线)确定理想的截断值。我们使用逻辑回归、Cox回归、对数秩检验和Kaplan-Meier方法分析NLR与患者疾病控制率(DCR)以及PFS或OS之间的关联。
NLR的理想阈值为2.826。NLR被确定为DCR的显著独立预测因子(OR = 0.17,95%CI = 0.05 - 0.48,p = 0.001),表明较高的NLR与较差的DCR相关。与淋巴细胞(AUC = 0.602)和中性粒细胞(AUC = 0.593)相比,NLR(AUC = 0.634)对DCR显示出更好的预测能力。高NLR值是PFS差(HR = 2.53,95%CI = 1.58 - 4.06,p < 0.001)和OS差(HR = 3.89,95%CI = 2.09 - 7.24,p < 0.001)的危险因素。
NLR升高与接受PD-L1抑制剂治疗的R/M NPC患者的治疗反应降低和生存率降低密切相关。NLR值高的患者疗效和生存率较差。