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. 2025 Jan 18:18:813-826.
doi: 10.2147/JIR.S496703. eCollection 2025.

The Clinical Value of the Combined Detection of Systemic Immune-Inflammation Index (SII), Systemic Inflammation Response Index (SIRI), and Prognostic Nutritional Index (PNI) in Early Diagnosis of Gastric Cancer

Affiliations

The Clinical Value of the Combined Detection of Systemic Immune-Inflammation Index (SII), Systemic Inflammation Response Index (SIRI), and Prognostic Nutritional Index (PNI) in Early Diagnosis of Gastric Cancer

Junyu Zheng et al. J Inflamm Res. .

Abstract

Objective: Gastric cancer (GC) is a common malignant tumor of the digestive tract. Accumulating studies suggest that inflammation is linked with the pathogenesis of GC. The study delves into novel hematological inflammatory markers, such as systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), and prognostic nutritional index (PNI), to explore their potential applications in early diagnosis of GC.

Methods: From October 2020 and August 2024, 1339 GC patients admitted to our hospital were enrolled in this study. The pre-treatment SII, SIRI, and PNI was calculated from peripheral blood samples. Univariate and multivariate logistic regression analyses were utilized to verify independent risk factors for patients, and constructed the nomograms. The correlation between hematological indicators and tumor-node-metastasis (TNM) stage was assessed through Spearman's analysis.

Results: Eligible patients and healthy controls were grouped by gender. The diagnostic ability of PNI was significantly superior to other indicators to diagnose male GC (area under the curve [AUC]=0.908, 95% CI: 0.892-0.925) and female GC (AUC=0.890, 95% CI: 0.865-0.914). Besides, the combination of hematological indicators is more effective in diagnosing GC patients, especially for male patients (AUC=0.916, 95% CI: 0.901-0.932, sensitivity: 84.98%, specificity: 84.29%). The C-statistic of Nomogram model was 0.917 for males and 0.875 for females. In both male and female cohorts, CEA, SII, and SIRI were positively correlated with TNM stage, while PNI was negatively correlated. The AUC of CEA, SII, SIRI, and PNI combined for the diagnosis in the early stage of male GC patients was 0.897 (95% CI: 0.875-0.918, sensitivity: 86.57%, specificity: 80.30%) is higher than that of in the advanced stage (AUC: 0.745, 95% CI: 0.710-0.780, sensitivity: 56.53%, specificity: 82.86%).

Conclusion: The combined CEA, SII, PNI, and SIRI could be used as screening biomarkers in diagnosing GC, especially in the early stage of male GC patients.

Keywords: PNI; SII; SIRI; early diagnosis; gastric cancer; prognostic nutritional index; systemic immune-inflammation index; systemic inflammation response index.

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Conflict of interest statement

All authors have no conflicts of interest of declare.

Figures

Figure 1
Figure 1
Flow diagram of subjects enrolled in this study.
Figure 2
Figure 2
ROC curves of hematological indicators for diagnosing GC (a and b) CEA, CA19-9, SII, SIRI and PNI in diagnosis of male GC patients. (c) Combined diagnostic value of CEA, CA19-9, SII, SIRI and PNI in male GC patients. (d and e) CEA, SII, SIRI and PNI in diagnosis of female GC patients. (f) Combined diagnostic value of CEA, SII, SIRI and PNI in female GC patients.
Figure 3
Figure 3
Nomogram to estimate the risk of patients with GC. (a) Nomogram model to predict male GC occurrence. (b) Nomogram model to predict female GC occurrence.
Figure 4
Figure 4
Correlation analysis of hematological indicators within Subgroups in male patients (ac) and female patients (df). A: 18–44 years old; B: 45–60 years old; C: 61–75 years old.
Figure 5
Figure 5
Association between TNM stage and CEA, SII, SIRI and PNI in male cohorts (ad) and female cohorts (eh) using Spearman’s analysis. 1: stage Ia, 2: stage Ib, 3: stage IIa, 4: stage IIb, 5: stage IIIa, 6: stage IIIb and 7: stage IIIc.
Figure 6
Figure 6
The ROC curves of hematological indicators for differentiating early stages or advanced stages GC from healthy control (a and b) In male GC cohorts and (c and d) In female GC cohorts.

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