Wu Zhong, Zhang Zongxin, Gu Chao
Clinical Laboratory, Nanxun District Hospital of Traditional Chinese Medicine, Huzhou, Zhejiang, 313009, China.
Clinical Laboratory, Huzhou Central Hospital, Affiliated Central Hospital of Huzhou University, Huzhou, Zhejiang, 313000, China.
Syst Rev. 2025 May 9;14(1):104. doi: 10.1186/s13643-025-02847-7.
Although the systemic inflammation response index (SIRI) is often associated with prognostic significance in esophageal cancer (EC) patients, the results continue to be conflicting. We focused on identifying SIRI's precise role in forecasting EC prognosis through performing this meta-analysis.
This work searched PubMed, Web of Science, Embase, Cochrane Library, and CNKI till November 16, 2024, and determined pooled hazard ratios (HRs) and 95% confidence intervals (CIs) for evaluating EC prognosis forecasting efficiency of SIRI. The inclusion criteria: (1) pathologic confirmation of EC; (2) those reporting associations of SIRI with EC survival outcomes; (3) those reporting HRs and 95% CIs; (4) those with an available cut-off value of SIRI; and (5) no restriction in language. The exclusion criteria: (1) case reports, reviews, meeting abstracts, comments and letters; (2) those enrolling duplicate cases; and (3) animal studies.
We enrolled six studies comprising 2176 cases into the present work. Based on our combined findings, elevated SIRI showed significant relation to dismal overall survival (OS) (HR = 1.43, 95%CI = 1.20-1.71, p < 0.001; I = 48.8%, p = 0.098) and shortened progression-free survival (PFS) (HR = 2.00, 95%CI = 1.35-2.98, p = 0.001; I = 0, p = 0.409) in EC. Moreover, high SIRI exhibited obvious relation to male gender (OR = 1.86, 95%CI = 1.07-3.22, p = 0.027; I = 69.4%, p = 0.020), TNM stage of III-IV (OR = 1.52, 95%CI = 1.18-1.94, p = 0.001; I = 24.3%, p = 0.265), T3-T4 stage (OR = 1.73, 95%CI = 1.12-2.69, p = 0.014; I = 61.0%, p = 0.053), and lymph node metastasis (OR = 1.29, 95%CI = 1.02-1.64, p = 0.036; I = 42.7%, p = 0.155). However, SIRI was not markedly related to age, tumor location, tumor differentiation, or smoking history.
In summary, high SIRI is significantly related to dismal OS and shortened PFS of EC cases, together with advanced tumor stage, T3-T4 stage, and lymph node metastasis of EC. Due to some limitations, large prospective studies that utilize standardized threshold SIRI should be conducted to validate our results in the future.
尽管全身炎症反应指数(SIRI)在食管癌(EC)患者中常与预后意义相关,但结果仍存在矛盾。我们通过进行这项荟萃分析,专注于确定SIRI在预测EC预后中的精确作用。
这项研究检索了截至2024年11月16日的PubMed、Web of Science、Embase、Cochrane图书馆和中国知网,并确定合并风险比(HRs)和95%置信区间(CIs),以评估SIRI对EC预后预测的效率。纳入标准:(1)EC的病理确诊;(2)报告SIRI与EC生存结果关联的研究;(3)报告HRs和95% CIs的研究;(4)有SIRI可用临界值的研究;(5)无语言限制。排除标准:(1)病例报告、综述、会议摘要、评论和信件;(2)纳入重复病例的研究;(3)动物研究。
我们纳入了6项研究,共2176例病例。基于我们的综合研究结果,SIRI升高与EC患者总体生存期(OS)不佳显著相关(HR = 1.43,95%CI = 1.20 - 1.71,p < 0.001;I = 48.8%,p = 0.098),无进展生存期(PFS)缩短(HR = 2.00,95%CI = 1.35 - 2.98,p = 0.001;I = 0,p = 0.409)。此外,高SIRI与男性性别(OR = 1.86,95%CI = 1.07 - 3.22,p = 0.027;I = 69.4%,p = 0.020)、TNM III - IV期(OR = 1.52,95%CI = 1.18 - 1.94,p = 0.001;I = 24.3%,p = 0.265)、T3 - T4期(OR = 1.73,95%CI = 1.12 - 2.69,p = 0.014;I = 61.0%,p = 0.053)以及淋巴结转移(OR = 1.29,95%CI = 1.02 - 1.64,p = 0.036;I = 42.7%,p = 0.155)存在明显关联。然而,SIRI与年龄、肿瘤位置、肿瘤分化或吸烟史无明显关联。
总之,高SIRI与EC患者的OS不佳和PFS缩短显著相关,同时与EC的肿瘤晚期、T3 - T4期和淋巴结转移相关。由于存在一些局限性,未来应进行利用标准化阈值SIRI的大型前瞻性研究以验证我们的结果。