Published online Jul 15, 2026. doi: 10.4251/wjgo.v18.i7.121250
Revised: April 8, 2026
Accepted: April 22, 2026
Published online: July 15, 2026
Processing time: 110 Days and 16.5 Hours
Hepatocellular carcinoma (HCC) prognosis is influenced by tumor burden, liver function, performance status, and systemic inflammation. Conventional prog
To evaluate the prognostic significance of the pan-immune-inflammation value (PIV) compared with ALBI and MELD-Na scores in patients with HCC.
This retrospective cohort study included 97 patients diagnosed with HCC and treated at the Medical Oncology Department of Ankara Etlik City Hospital between September 2022 and September 2025. Overall survival (OS) was analyzed using Kaplan-Meier survival analysis, Cox regression models, and receiver operating characteristic (ROC) curve analysis. Univariate and multivariable Cox regression analyses were performed to identify independent prognostic factors, and optimal cut-off values were determined using the Youden index.
Median follow-up was 10 months, and 58 deaths occurred. In univariate analysis, Eastern Cooperative Oncology Group (ECOG) performance status, Barcelona clinic liver cancer stage, cirrhosis, treatment modality, ALBI, MELD-Na score, and PIV were significantly associated with OS (all P < 0.05). In multivariable Cox regression analysis, ECOG performance status (P < 0.001) and PIV (P = 0.016) remained independent prognostic factors. ROC analysis demonstrated that PIV had the highest discriminatory ability for predicting OS (AUC = 0.794, P < 0.001), followed by ALBI (AUC = 0.781, P < 0.001), alpha-fetoprotein (AUC = 0.712, P < 0.001), and MELD-Na (AUC = 0.699, P = 0.001). Patients with high PIV had significantly poorer survival, with a median OS of 5 months compared with 30 months in the low-PIV group.
These findings demonstrate that PIV provides superior prognostic performance compared with conventional liver function-based scores and may serve as a robust biomarker for risk stratification in patients with HCC.
Core Tip: Pan-immune-inflammation value (PIV) is a novel biomarker reflecting systemic inflammatory and immune status in hepatocellular carcinoma (HCC). In this retrospective study, PIV demonstrated superior prognostic performance compared with conventional liver function scores such as albumin-bilirubin and model for end-stage liver disease-sodium and remained an independent predictor of overall survival. These findings suggest that inflammation-based indices may improve risk stratification beyond traditional liver function-based models in patients with HCC.