Published online Sep 15, 2026. doi: 10.4251/wjgo.119082
Revised: March 28, 2026
Accepted: May 14, 2026
Published online: September 15, 2026
Processing time: 213 Days and 4.5 Hours
High Ki-67 expression promotes epithelial-mesenchymal transition and angio
To validate the interrelationships within the “Edmondson grade-MVI-SN-Ki-67” aggressive pathological cluster and to evaluate the predictive value of Ki-67 for SN.
A retrospective analysis was conducted on 223 patients with HCC who under
The pathological features demonstrated strong intercorrelations, with MVI and SN exhibiting the strongest association (rs = 0.637, odds ratio = 75.833). Ki-67 displayed optimal and consistent predictive performance for SN positivity across both centers (area under the curve = 0.792). A uniform Ki-67 cutoff value of 32.5% was identified, yielding high specificity (0.813). The predictive performance of Ki-67 for SN showed no significant difference between centers (area under the curve = 0.780 vs 0.835, P = 0.372). In multivariate analysis, Ki-67 remained an independent predictor of SN after adjusting for study center (odds ratio = 1.058, P < 0.001).
Key pathological characteristics of HCC constitute a tightly linked aggressive cluster. Ki-67 serves as a reproducible predictive biomarker for SN positivity, providing validated multicenter pathological evidence for postoperative risk stratification.
Core Tip: This dual-center retrospective study validates a tightly linked aggressive pathological cluster (Edmondson grade, microvascular invasion, satellite nodules, Ki-67) in hepatocellular carcinoma. We identify Ki-67 as a core, reproducible biomarker, with a validated cutoff of 32.5% demonstrating high specificity (0.813) for predicting satellite nodules positivity across two independent centers. These findings provide multicenter pathological evidence to inform postoperative risk stratification and adjuvant therapy decisions.