赵小涵, 沈文斌, 祝淑钗, 王鹤松, 宋春洋, 邓文钊. 营养免疫炎性指标预测免疫联合放化疗二线治疗食管鳞癌患者预后的价值[J]. 中国肿瘤临床, 2023, 50(14): 720-727. DOI: 10.12354/j.issn.1000-8179.2023.20230297
引用本文: 赵小涵, 沈文斌, 祝淑钗, 王鹤松, 宋春洋, 邓文钊. 营养免疫炎性指标预测免疫联合放化疗二线治疗食管鳞癌患者预后的价值[J]. 中国肿瘤临床, 2023, 50(14): 720-727. DOI: 10.12354/j.issn.1000-8179.2023.20230297
Xiaohan Zhao, Wenbin Shen, Shuchai Zhu, Hesong Wang, Chunyang Song, Wenzhao Deng. The prognostic value of nutritional immunoinflammatory indicators for patients withesophageal squamous cell carcinoma treated with second-line immunotherapycombined with radio (chemo) therapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2023, 50(14): 720-727. DOI: 10.12354/j.issn.1000-8179.2023.20230297
Citation: Xiaohan Zhao, Wenbin Shen, Shuchai Zhu, Hesong Wang, Chunyang Song, Wenzhao Deng. The prognostic value of nutritional immunoinflammatory indicators for patients withesophageal squamous cell carcinoma treated with second-line immunotherapycombined with radio (chemo) therapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2023, 50(14): 720-727. DOI: 10.12354/j.issn.1000-8179.2023.20230297

营养免疫炎性指标预测免疫联合放化疗二线治疗食管鳞癌患者预后的价值

The prognostic value of nutritional immunoinflammatory indicators for patients withesophageal squamous cell carcinoma treated with second-line immunotherapycombined with radio (chemo) therapy

  • 摘要:
      目的  评估营养免疫炎性指标用于预测接受camrelizumab联合放(化)疗二线治疗复发和(或)转移转移食管鳞癌(relapsed or metastatic esophageal squamous cell carcinoma ,R/M ESCC)患者预后的价值。
      方法  从2018年1月至2021年3月,从河北医科大学第四医院筛选出48例符合入组标准的R/M ESCC患者进行回顾性分析,根据受试者工作特征曲线(receiver operating characteristic curve,ROC)确定预后营养指数(prognostic nutritional index, PNI)、中性粒细胞淋巴细胞比(neutrophilic-to-lymphocyte ratio,NLR)、血小板与淋巴细胞比(platelet-to-lymphocyte ratio,PLR)和全身免疫-炎症指数(systemic immune-inflammation index,SII)这4项指标预测患者预后的最佳临界值。应用SPSS 25.0版本软件进行单因素和多因素统计学分析。
      结果  全组患者二线免疫治疗后的1、2年生存(overall survival,OS)率和无进展生存(progression-free survival,PFS)率分别为42.9%、22.5%和29.0%、5.8%;中位OS和PFS分别为9.0个月(95%CI:6.4~11.7)和8.5个月(95%CI:1.5~5.6)。多因素分析结果显示免疫联合方式、近期疗效、PNI、NLR、PLR和SII为患者OS的独立影响因素(P=0.044、0.030、<0.001、0.040、0.044、0.036);免疫联合方式、使用免疫周期数、近期疗效、PNI、NLR、PLR和SII为患者PFS的独立影响因素(P=0.049、0.024、0.003、0.017、0.008、<0.001、0.009)。
      结论  低PNL,高NLR、PLR和SII值为接受camrelizumab联合放(化)疗二线治疗R/M ESCC预后较差的独立性预测指标。

     

    Abstract: Objective: To evaluate the value of serological nutritional immunoinflammatory indicators for predicting the prognosis of patients with relapsed or metastatic esophageal squamous cell carcinoma (R/M ESCC) treated with camrelizumab combined with radio (chemo) therapy. Methods: From January 2018 to March 2021, 48 R/M ESCC patients who met the inclusion criteria were screened from The Forth Hospital of Hebei Medical University for retrospective analysis. According to the receiver operating characteristics (ROC) curve, the optimal threshold values of the prognostic nutritional index (PNI), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and systemic immune-inflammation index (SII) were determined. SPSS 25.0 software was used to perform univariate and multivariate statistical analyses. Results: The one- and two-year rates of overall survival (OS) and progression-free survival (PFS) after second-line immunotherapy were 42.9%, 22.5%, and 29.0%, 5.8%, respectively. The median OS and PFS were 9.0 months (95%CI: 6.4–11.7) and 8.5 months (95%CI:1.5–5.6), respectively. The multivariate analysis results showed that the combined methods of immunization, short-term efficacy, PNI, NLR, PLR, and SII were independent prognostic factors affecting patients’ OS (P=0.044, 0.030, 0.000, 0.040, 0.044, and 0.036, respectively). The independent prognostic factors for PFS were the combined methods of immunization, number of immunotherapy cycles, short-term efficacy, PNI, NLR, PLR, and SII (P=0.049, 0.024, 0.003, 0.017, 0.008, 0.000, and 0.009, respectively). Conclusions: Low PNL, high NLR, PLR, and SII values are independent predictors of poor prognosis for R/M ESCC after second-line therapy with a combination of camrelizumab and radiotherapy. alues are independent predictors of poor prognosis for R/M ESCC after second-line therapy with a combination of camrelizumab and radiotherapy.

     

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