Pan-immune-inflammation value as a novel prognostic biomarker for digestive system cancers: a meta-analysis

World J Surg Oncol. 2024 Nov 20;22(1):306. doi: 10.1186/s12957-024-03595-z.

Abstract

Background: Digestive system cancers pose a significant global health challenge with high incidence and mortality rates. Inflammation is a key factor in cancer progression, necessitating reliable prognostic indicators. The pan-immune-inflammation value (PIV), as a new biomarker of immune-inflammatory response, has emerged as a potential prognostic biomarker for cancers.

Methods: We performed a meta-analysis to evaluate the prognostic significance of PIV in digestive system cancers. Our search, up to June 2024, included 20 studies from 19 articles with 5037 patients. We extracted and analyzed data on PIV levels and assessed hazard ratios (HRs) for overall survival (OS), progression-free survival (PFS), disease-free survival (DFS), recurrence-free survival (RFS), and cancer-specific survival (CSS) using STATA 14.0.

Results: Our analysis found that high PIV levels were significantly associated with poor prognosis in patients with digestive system cancers. Specifically, high PIV was linked to shorter OS (HR = 2.039, P < 0.001), PFS (HR = 1.877, P = 0.028), DFS (HR = 1.624, P = 0.005), RFS (HR = 2.393, P = 0.037), and CSS (HR = 2.053, P < 0.001). Additionally, the adverse prognostic impact of high PIV on OS was consistent across different cancer types, including digestive tract, colorectal, esophageal, and hepatobiliary pancreatic cancers. Although some heterogeneity was observed, sensitivity and bias analyses confirmed the reliability of these findings.

Conclusions: PIV was a valuable and practical prognostic marker for digestive system cancers, providing significant predictive value across multiple survival metrics. Its simplicity and minimal invasiveness nature support its potential integration into routine clinical practice.

Keywords: Biomarker; Cancer; Meta-analysis; Pan-immune-inflammation value; Prognosis.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Biomarkers, Tumor* / analysis
  • Digestive System Neoplasms* / diagnosis
  • Digestive System Neoplasms* / immunology
  • Digestive System Neoplasms* / mortality
  • Digestive System Neoplasms* / pathology
  • Humans
  • Inflammation* / immunology
  • Prognosis
  • Survival Rate

Substances

  • Biomarkers, Tumor