Yang Ruonan, Chang Qian, Meng Xianchun, Gao Nan, Wang Wanhai
Clinical Laboratory, First Affiliated Hospital of Zhengzhou University, Key Laboratory of Laboratory Medicine of Henan Province, Zhengzhou, Henan, People's Republic of China.
J Cancer. 2018 Sep 7;9(18):3295-3302. doi: 10.7150/jca.25691. eCollection 2018.
Systemic immune-inflammation index (SII), on the basis of lymphocyte, neutrophil and platelet counts had been published to be a good prognostic factor in multiple cancers. Nevertheless, the prognostic value of SII in cancer patients remains inconsistent. Therefore, we carried out a meta-analysis to evaluate the prognostic value of SII in these patients with cancer. A total of 22 articles with 7657 patients enrolled in this meta-analysis. The combined result revealed that a high SII was evidently correlated with poor overall survival (OS) (HR=1.69, 95%CI=1.42-2.01, <0.001), poor time to recurrent (TTR) (HR=1.87, <0.001) , poor progress-free survival (PFS) (HR=1.61, =0.012) ,poor cancer-specific survival (CSS) (HR=1.44, =0.027) , poor relapse-free survival (RFS) (HR=1.66, =0.025) and poor disease-free survival (DFS) (HR=2.70, <0.001) in patients with cancers. Subgroup analysis indicated that SII over the cutoff value could predict worse overall survival in Hepatocellular carcinoma (<0.001), Gastric cancer (=0.005), Esophageal Squamous Cell Carcinoma (=0.013), Urinary system cancer (<0.001), Small cell lung cancer (<0.001), Non-Small cell lung cancer (<0.001) and Acral Melanoma (<0.001). The largest effect size was observed in the Hepatocellular carcinoma (HR=2.11). In addition, these associations did not vary significantly by the cutoff value, sample size and ethnicity. Therefore, high SII may be a potential prognostic marker in patients with various cancers and associated with the poor overall outcomes.
基于淋巴细胞、中性粒细胞和血小板计数的全身免疫炎症指数(SII)已被公布为多种癌症的良好预后因素。然而,SII在癌症患者中的预后价值仍不一致。因此,我们进行了一项荟萃分析,以评估SII在这些癌症患者中的预后价值。本荟萃分析共纳入22篇文章,7657例患者。综合结果显示,高SII与总体生存率(OS)差(HR=1.69,95%CI=1.42-2.01,<0.001)、复发时间(TTR)差(HR=1.87,<0.001)、无进展生存期(PFS)差(HR=1.61,=0.012)、癌症特异性生存期(CSS)差(HR=1.44,=0.027)、无复发生存期(RFS)差(HR=1.66,=0.025)和无病生存期(DFS)差(HR=2.70,<0.001)显著相关。亚组分析表明,SII超过临界值可预测肝细胞癌(<0.001)、胃癌(=0.005)、食管鳞状细胞癌(=0.013)、泌尿系统癌(<0.001)、小细胞肺癌(<0.001)、非小细胞肺癌(<0.001)和肢端黑色素瘤(<0.001)的总体生存率更差。在肝细胞癌中观察到最大的效应量(HR=2.11)。此外,这些关联在临界值、样本量和种族方面没有显著差异。因此,高SII可能是各类癌症患者的潜在预后标志物,并与不良的总体预后相关。