Zhou Yun, Liu Xia, Wu Biwen, Li Jiajun, Yi Zexin, Chen Cunte, Wu Yong, Liu Guolong, Wang Peipei
Department of Oncology, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, Guangdong, China.
Department of Oncology, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, Guangdong, China; The First Affiliated Hospital, Jinan University, Guangzhou, Guangdong, China.
Int Immunopharmacol. 2025 Mar 6;149:114215. doi: 10.1016/j.intimp.2025.114215. Epub 2025 Feb 3.
Due to drug resistance, a majority of patients with non-small cell lung cancer (NSCLC) experience disease progression following immunotherapy. Therefore, there is an urgent need to develop novel biomarkers to predict the prognosis of NSCLC patients. Clinical data from 544 patients with advanced NSCLC who underwent immune checkpoint blockers (ICBs) at our clinical center were collected in this study. The results indicated that low Albumin-Globulin Ratio (AGR) and Lymphocyte-Monocyte Ratio (LMR) and high Systemic Immune-Inflammation Index (SIRI) were significantly correlated with both poor overall survival (OS) and progression-free survival (PFS) in NSCLC patients (P < 0.01). These three indicators collectively formed the most effective combined model for predicting the prognosis of NSCLC. Importantly, risk stratification based on AGR, LMR and SIRI was better than that based on the TNM stage, and served as an independent predictor of OS and PFS. Notably, the nomogram model developed by risk stratification, sex, age, smoking history, and pathological type demonstrated a good ability to predict the 1 to 5-year OS rates for NSCLC patients. In summary, AGR, LMR, and SIRI represented the optimal combined models for forecasting the prognosis of patients with advanced NSCLC who underwent ICBs, offering promising potential as biomarkers to direct personalized clinical interventions.
由于耐药性,大多数非小细胞肺癌(NSCLC)患者在免疫治疗后会出现疾病进展。因此,迫切需要开发新的生物标志物来预测NSCLC患者的预后。本研究收集了在我们临床中心接受免疫检查点阻断剂(ICB)治疗的544例晚期NSCLC患者的临床数据。结果表明,低白蛋白球蛋白比(AGR)、淋巴细胞单核细胞比(LMR)和高全身免疫炎症指数(SIRI)与NSCLC患者较差的总生存期(OS)和无进展生存期(PFS)均显著相关(P < 0.01)。这三个指标共同构成了预测NSCLC预后最有效的联合模型。重要的是,基于AGR、LMR和SIRI的风险分层优于基于TNM分期的风险分层,并可作为OS和PFS的独立预测指标。值得注意的是,由风险分层、性别、年龄、吸烟史和病理类型构建的列线图模型对NSCLC患者1至5年的OS率具有良好的预测能力。总之,AGR、LMR和SIRI是预测接受ICB治疗的晚期NSCLC患者预后的最佳联合模型,作为指导个性化临床干预的生物标志物具有广阔前景。