纵向血浆代谢组学指导食管鳞状细胞癌化疗免疫治疗的动态风险评估与饮食调节
Longitudinal Plasma Metabolomics Guides Dynamic Risk Assessment and Dietary Modulation for Esophageal Squamous Cell Cancer Chemoimmunotherapy.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Pan-immune-inflammation Value and Prognosis in Patients With Esophageal Cancer.
Pan-immune-inflammation Value and Prognosis in Patients With Esophageal Cancer.
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PIV 与食管癌的临床结局相关,支持其作为预后生物标志物的作用。
评估 866 例食管癌患者的全身免疫炎症值(PIV)、肿瘤免疫和临床结局之间的关系。
PIV 根据外周血计数中所有免疫炎症细胞计算,是近期提出的一种用于部分癌症临床结局评估的指标,但其在食管癌中的预后意义仍不清楚。
在推导队列(n = 433)中,利用时间依赖性受试者工作特征(ROC)曲线确定最佳截断值;在验证队列(n = 433)中,考察 PIV 与TIL(肿瘤浸润淋巴细胞)、免疫组化染色显示的 CD8 表达及患者预后的关系。
推导队列中,PIV 的 5 年 ROC 曲线下面积为 0.631。验证队列分为 PIV 低值组(n = 223)和高值组(n = 210);低值组总生存期显著更差(log-rank P = 0.0065;风险比 [HR]:1.48;95% 置信区间 [CI]:1.12–1.98;P < 0.001;多变量 HR:1.41;95% CI:1.05–1.90;P = 0.023)。任何临床特征均未显著改变 PIV 的预后效应(交互作用 P > 0.05)。PIV 高值与 TIL 状态较低(P < 0.001)及 CD8 阳性细胞计数较低(P = 0.011)显著相关。
PIV 与食管癌临床结局相关,支持其作为预后生物标志物的作用。考虑到 PIV 与 TIL 的关系,全身免疫能力可能通过局部免疫反应影响患者预后。
To examine the relationship between the pan-immune-inflammation value (PIV), tumor immunity, and clinical outcomes in 866 patients with esophageal cancer.
The PIV, calculated from all immune-inflammatory cells in the peripheral blood count, is a recently proposed marker for clinical outcomes in some types of cancers. Nonetheless, the prognostic significance of PIV in esophageal cancer remains unclear.
In the derivation cohort (n = 433), we set the optimal cutoff value using a time-dependent receiver operating characteristic (ROC) curve. In the validation cohort (n = 433), the relationships between the PIV, tumor-infiltrating lymphocytes (TILs), CD8 expression by immunohistochemical staining, and patient prognosis were examined.
The area under the ROC curve for the PIV at 5 years was 0.631 in the derivation cohort. The validation cohort, divided into PIV-low cases (n = 223) and PIV-high cases (n = 210), showed significantly worse overall survival (log-rank P = 0.0065; hazard ratio [HR]: 1.48; 95% confidence interval [CI]: 1.12-1.98; P < 0.001; multivariate HR: 1.41; 95% CI: 1.05-1.90; P = 0.023). The prognostic effect of the PIV was not significantly modified by any clinical characteristics ( P for interaction > 0.05). The PIV-high cases were significantly associated with a low TIL status ( P < 0.001) and low CD8-positive cell counts ( P = 0.011).
The PIV was associated with clinical outcomes in esophageal cancer, supporting its role as a prognostic biomarker. Considering the relationship between the PIV and TILs, systemic immune competence may influence patient prognosis through a local immune response.
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