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Systemic inflammation with sarcopenia predicts survival in patients with gastric cancer

内科学 医学 肌萎缩 癌症 比例危险模型 多元分析 胃肠病学 接收机工作特性 单变量分析 生存分析 肿瘤科
作者
Yuying Liu,Guo‐Tian Ruan,Yi‐Zhong Ge,Qin‐Qin Li,Qi Zhang,Xi Zhang,Meng Tang,Mengmeng Song,Xiaowei Zhang,Xiangrui Li,Kang‐Ping Zhang,Ming Yang,Chunlei Hu,Tong Liu,Hailun Xie,Xiaoyue Liu,Shiqi Lin,Min Weng,Qinghua Yao,Zhengping Wang
出处
期刊:Journal of Cancer Research and Clinical Oncology [Springer Nature]
卷期号:149 (3): 1249-1259 被引量:20
标识
DOI:10.1007/s00432-022-03925-2
摘要

ObjectiveThe levels of platelet-related inflammation indicators and sarcopenia have been reported to affect the survival of patients with cancer. To evaluate the prognostic influence of platelet count (PLT), platelet lymphocyte ratio (PLR), and systemic immune inflammation index (SII), and SII combined with sarcopenia on the survival of patients with gastric cancer (GC).MethodsA total of 1133 patients with GC (812 male and 321 female, average age: 59.43 years) were evaluated. Receiver-operating characteristic curves were used to determine the best cutoff values of PLT, PLR, and SII, and univariate and multivariate Cox risk regression models were used to evaluate whether SII is an independent predictor of overall survival (OS). The prognostic SS (SII-sarcopenia) was established based on SII and sarcopenia. Finally, a comprehensive analysis of the prognostic SS was performed.ResultsSII had the strongest prognostic effect. The SII and OS of patients with GC were in an inverted U-shape (adjusted HR = 1.07; 95% CI 0.97–1.19; adjusted P = 0.179). In patients with SII > 1800, SII was negatively correlated with OS (adjusted HR = 0.57; 95% CI 0.29–1.12; adjusted P = 0.102), however, there is no statistical difference. Interestingly, a high SS was associated with a poorer prognosis. The higher the SS score was, the worse the OS (P < 0.001).ConclusionSII is an independent prognostic indicator of GC, and high SII is related to poor prognosis. A higher SS score had worse survival. Thus, the prognostic SS is a reliable predictor of OS in patients with GC.

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