首页|期刊导航|疑难病杂志|肺部免疫预后指数联合血清sTNFR2对非小细胞肺癌患者化疗并发骨髓抑制的预测价值

肺部免疫预后指数联合血清sTNFR2对非小细胞肺癌患者化疗并发骨髓抑制的预测价值OA

The predictive value of the pulmonary immune prognostic index combined with serum sTNFR2 for bone marrow suppression complicated by chemotherapy in patients with non-small cell lung cancer

中文摘要英文摘要

目的 探讨肺部免疫预后指数(LIPI)联合血清可溶性肿瘤坏死因子受体2(sTNFR2)对非小细胞肺癌(NSCLC)患者化疗并发骨髓抑制的预测价值.方法 回顾性选取2022年1月-2025年1月安徽医科大学附属宿州医院呼吸与危重症医学科接受化疗的NSCLC患者92例作为研究对象,根据化疗后是否发生骨髓抑制分为骨髓抑制组63例和无骨髓抑制组29例.检测患者中性粒细胞计数(Neu)、白细胞计数(WBC)、乳酸脱氢酶(LDH),计算中性粒细胞/淋巴细胞(LYM)比值(dNLR),并按改良标准评定LIPI评分;ELISA法检测血清sTNFR2水平;多因素Logistic回归分析NSCLC患者化疗并发骨髓抑制的影响因素;受试者工作特征(ROC)曲线评估LIPI联合血清sTNFR2对NSCLC患者化疗并发骨髓抑制的预测效能.结果 骨髓抑制组血清sTNFR2水平高于无骨髓抑制组(t/P=6.235/<0.001);骨髓抑制组LIPI及相关指标(dNLR、Neu、WBC、LDH、ALT、SCr)均高于无骨髓抑制组(t/P=5.218/<0.001、5.873/<0.001、4.592/<0.001、3.586/0.001、5.012/<0.001、2.648/<0.001、2.715/0.008);含铂双药化疗方案、LIPI 评分高、sTNFR2高是NSCLC患者化疗并发骨髓抑制的独立危险因素[OR(95%CI)=2.689(1.215~5.947)、2.518(1.423~4.451)、1.852(1.236~2.778)];LIPI、血清sTNFR2水平单独及二者联合预测NSCLC患者化疗并发骨髓抑制的AUC分别为0.775、0.816、0.903,二者联合优于各自单独预测效能(Z/P=2.345/0.019、1.987/0.047).结论 LIPI联合血清sTNFR2可有效提升对NSCLC患者化疗相关骨髓抑制的预测效能,为临床风险分层提供更精准的依据.

Objective To explore the predictive value of the lung immune prognostic index(LIPI)combined with serum soluble tumor necrosis factor receptor 2(sTNFR2)for bone marrow suppression complicated by chemotherapy in pa-tients with non-small cell lung cancer(NSCLC).Methods A total of 92 patients with NSCLC who received chemotherapy were included and divided into a myelosuppression group(63 cases)and a non-myelosuppression group(29 cases)according to whether myelosuppression occurred after chemotherapy.Fasting venous blood was collected from all patients within 24 hours of admission.Absolute neutrophil count(Neu),total white blood cell count(WBC),and lactate dehydrogenase(LDH)were detected by an automatic analyzer.The derived neutrophil-to-lymphocyte ratio(dNLR=Neu/(WBC-Neu))was calculat-ed,and the LIPI score was evaluated according to the modified criteria.Serum sTNFR2 levels were detected by ELISA.The t-test/Wilcoxon rank sum test and x2 test were used to compare baseline indicators between the two groups.Multivariate logis-tic regression analysis was used to identify independent risk factors.ROC curves were used to evaluate predictive efficacy.Re-sults Serum sTNFR2 level in the myelosuppression group was(2.41±0.76)ng/mL,which was significantly higher than that in the non-myelosuppression group[(1.45±0.52)ng/mL](t=6.235,P<0.001).LIPI-related indicators(dNLR,Neu,WBC,LDH),sTNFR2,ALT,and Cr in the myelosuppression group were all significantly higher than those in the non-myelosuppres-sion group(t=5.873,4.592,3.586,5.012,6.235,2.648,2.715,all P<0.001).High LIPI score,high serum sTNFR2,and plati-num-based dual-drug chemotherapy regimens were independent risk factors for bone marrow suppression complicated by chemotherapy in NSCLC patients[OR(95%CI)=2.518(1.423-4.451),1.852(1.236-2.778),2.689(1.215-5.947);P=0.002,0.003,0.015].The AUCs of LIPI,serum sTNFR2,and their combination in predicting bone marrow suppression complicated by chemotherapy in NSCLC patients were 0.775,0.816,and 0.903,respectively.The combined predictive efficacy of the two was superior to that of each individual(differences were compared using the DeLong method)(Z=2.345,1.987;P=0.019,0.047).Conclusion The LIPI score combined with serum sTNFR2 can effectively enhance the predictive efficacy of bone marrow suppression during chemotherapy in NSCLC patients,providing a precise basis for clinical risk stratification.

李磊;程英;孙传忠;郭锋;王震

234000 安徽宿州,安徽医科大学附属宿州医院/宿州市立医院呼吸与危重症医学科234000 安徽宿州,安徽医科大学附属宿州医院/宿州市立医院呼吸与危重症医学科234000 安徽宿州,安徽医科大学附属宿州医院/宿州市立医院呼吸与危重症医学科234000 安徽宿州,安徽医科大学附属宿州医院/宿州市立医院呼吸与危重症医学科234000 安徽宿州,安徽医科大学附属宿州医院/宿州市立医院呼吸与危重症医学科

医药卫生

非小细胞肺癌肺部免疫预后指数可溶性肿瘤坏死因子受体2化疗骨髓抑制预测价值

Non-small cell lung cancerLung immune prognostic indexSerum soluble tumor necrosis factor recep-tor 2ChemotherapyBone marrow suppressionPrediction

《疑难病杂志》 2026 (4)

390-394,5

安徽省重点研究与开发项目(2022e07020010) Key Research and Development Projects of Anhui Province(2022e07020010)

10.3969/j.issn.1671-6450.2026.04.002

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