Published online Nov 15, 2026. doi: 10.4251/wjgo.122505
Revised: July 24, 2026
Accepted: September 18, 2026
Published online: November 15, 2026
Processing time: 189 Days and 14.7 Hours
Colorectal cancer (CRC) remains a leading cause of cancer-related mortality worldwide, making early detection of precancerous adenomas critical for effective prevention. The systemic immune-inflammation index (SII), derived from peri
To investigate the clinical utility of SII in screening for CRC and precancerous adenomas, and to evaluate its association with pathological features and prog
This retrospective study included 332 patients (141 with CRC, 191 with colorectal adenoma) who underwent colonoscopy between January 2019 and June 2025. Pe
SII was significantly higher in CRC than that in adenomas [712.76 (IQR: 435.87-1586.92) vs 347.56 (IQR: 256.05-471.03), P < 0.001]. The optimal SII cut-off for distinguishing CRC from adenoma was 480.326 [area under the curve (AUC) = 0.801, sensitivity 72.3%, specificity 76.1%]. Multivariate logistic regression confirmed that elevated SII [per 100-unit increase: Odds ratio (OR) = 1.195, 95% confidence interval: 1.101-1.298, P < 0.001], NLR (OR = 1.489, P < 0.001), PLR (OR = 1.009, P < 0.001), and CRP (OR = 1.069, P = 0.003) were independent risk factors for CRC after adjusting for age, hemoglobin, carcinoembryonic antigen, and fecal immunochemical test. For predicting lymph node meta
Elevated SII is an independent risk factor for CRC and may serve as a useful auxiliary screening marker. Preope
Core Tip: This retrospective study explored the clinical value of systemic immune-inflammation index (SII) screening and assessing colorectal adenoma and colorectal cancer (CRC). Receiver operating characteristic curve determined SII’s diag