炎症营养因素对中晚期非小细胞肺癌患者免疫治疗效果的预测价值
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安徽省高等学校自然科学研究项目(KJ2020A0338)


Predictive value of inflammatory nutritional indices for immunotherapy in patients with advanced non-small cell lung cancer
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    摘要:

    目的 探讨炎症营养因素对中晚期非小细胞肺癌(NSCLC)患者接受程序性死亡受体1(PD-1)抑制剂治疗疗效的预测价值。方法 回顾性分析2020年7月—2023年11月安徽理工大学第一附属医院收治的接受PD-1抑制剂免疫治疗的70例中晚期NSCLC患者的完整病历资料。根据受试者工作特征(ROC)曲线获得血清C反应蛋白(CRP)、C反应蛋白与白蛋白比值(CAR)的最佳截断值,并根据最佳截断值将患者分别分为高CRP(H-CRP)、低CRP(L-CRP)组和高CAR(H-CAR)、低CAR(L-CAR)组;根据格拉斯哥预后评分(GPS)分为GPS0组、GPS1组和GPS2组。使用卡方检验对组间各临床特征的分类变量进行差异分析。采用卡方检验分析各组间经免疫治疗后的客观缓解率(ORR)、疾病控制率(DCR)。通过Kaplan-Meier方法进行生存分析,单因素和多因素Cox分析筛选影响患者无进展生存期(PFS)的独立危险因素。通过R软件建立临床预测模型列线图,并进行模型评价及内部验证。通过Kaplan-Meier方法进行生存分析,单因素和多因素Cox分析筛选影响患者PFS的独立危险因素。通过R软件建立临床预测模型列线图,并进行模型评价及内部验证。结果 GPS与免疫治疗药物有相关性(P=0.004)。CRP、CAR、GPS组间ORR均无显著相关性(P>0.05);L-CRP、L-CAR组较H-CRP、H-CAR组DCR显著升高(P=0.002、P=0.001),GPS0的患者DCR显著升高(P=0.005)。Kaplan-Meier生存分析表明L-CRP组中位PFS(mPFS)14.77个月,显著高于H-CRP组mPFS 6.13个月(P=0.001 7)。L-CAR组mPFS 24.53个月,显著高于H-CAR组5.63个月(P<0.001)。GPS 0组mPFS 13.83个月,显著高于GPS 1组的5.63个月和GPS 2组的8.40个月(P=0.041)。多因素Cox分析表明CAR是接受PD-1抑制剂治疗的NSCLC患者PFS的独立预后因素(P=0.001)。通过R软件将CRP、CAR、GPS纳入构建临床预测模型,经检验该模型具有较好的预测价值。结论 使用血清CRP、CAR及GPS构建临床预测模型,这个模型具有很好的区分度和校准度,对用于预测中晚期NSCLC抗PD-1治疗效果具有重要价值

    Abstract:

    Objective The objective of this study was to investigate the predictive value of inflammatory and nutritional factors in PD-1 inhibitor treatment in patients with advanced non-small cell lung cancer (NSCLC).Methods The complete medical records of 70 patients with advanced NSCLC treated with PD-1 inhibitor immunotherapy in the First Affiliated Hospital of Anhui University of Science and Technology from July 2020 to November 2023 were retrospectively analyzed. Survival analysis was performed by Kaplan-Meier method, and univariate and multivariate Cox analysis was used to screen for independent risk factors affecting patients' PFS. RStudio was used to build the clinical prediction model, and C-index, ROC curve, calibration curve and DCA curve were used to evaluate the model, and bootstrap method was used for internal verification. Results There was no significant correlation between CRP, CAR, GPS and ORR (P>0.05). The DCR of low CRP and CAR was significantly increased (P=0.002, P=0.001), and DCR of patients with low GPS was significantly increased (P=0.005). Kaplan-Meier survival analysis showed that the median PFS (mPFS) of L-CRP group was 14.77 months, which was significantly higher than that of H-CRP group (P=0.002). The mPFS of L-CAR group was 24.53 months, which was significantly higher than that of H-CAR group which was 5.63 months (P<0.001). mPFS of 13.83 months in the GPS 0 group was significantly higher than 5.63 months in the GPS 1 group and 8.40 months in the GPS 2 group (P=0.041). Multivariate Cox analysis showed that CAR (P=0.001) was an independent prognostic factor for PFS in NSCLC patients treated with PD-1 inhibitors. CRP, CAR and GPS in this study were incorporated into the clinical prediction model by RStudio, and the model was tested to have good predictive value.Conclusion In this study, serum CRP, CAR and GPS were used to construct a clinical prediction model, which has good differentiation and calibration degree, and is of great value for predicting the anti-PD-1 treatment effect of middle and advanced NSCLC

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  • 在线发布日期: 2025-12-19
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