# Predictive value of geriatric nutritional risk index in patients with pancreatic cancer: a meta-analysis

**Authors:** Yaqi Hua, Yi Yuan, Chen Zhou, Liping Liu, Yan Hu, Ping Tu, Dongying Li

PMC · DOI: 10.3389/fnut.2025.1464447 · Frontiers in Nutrition · 2025-07-29

## TL;DR

This study finds that the Geriatric Nutritional Risk Index can predict survival and complications in pancreatic cancer patients.

## Contribution

The study is the first meta-analysis to evaluate GNRI's predictive value specifically for pancreatic cancer outcomes.

## Key findings

- Lower GNRI scores are strongly linked to worse overall survival in pancreatic cancer patients.
- GNRI effectively predicts the risk of postoperative pancreatic fistula.
- No significant association was found between GNRI and postoperative hemorrhage.

## Abstract

While growing evidence supports the Geriatric Nutritional Risk Index (GNRI) as a prognostic indicator for various cancers, its predictive value in pancreatic cancer remains unclear. This meta-analysis systematically evaluates GNRI’s ability to predict postoperative complications and long-term outcomes in pancreatic cancer patients.

We conducted a comprehensive literature search across nine databases (Web of Science, PubMed, Embase, Cochrane Library, Scopus, WanFang, CNKI, VIP, and SinoMed) through June 1, 2025. Hazard ratios (HRs) with 95% confidence intervals (CIs) were used to assess overall survival (OS), while risk ratios (RRs) with 95% CIs evaluated postoperative complications.

From 233 initially identified studies, 10 met inclusion criteria (n = 2,003 patients). Pooled analysis revealed that lower GNRI significantly predicted worse OS (HR = 1.92, 95% CI 1.54–2.41, p < 0.0001) and higher postoperative pancreatic fistula (POPF) incidence (RR = 0.18, 95% CI 0.08–0.43, p < 0.001). No significant association was found between GNRI and post-pancreatectomy hemorrhage (PPH) (RR = 0.21, 95% CI 0.03–1.53, p = 0.13).

GNRI shows promise as a clinically useful predictor of OS and POPF in pancreatic cancer patients. However, these findings require validation through prospective multicenter studies.

Identifier CRD42023409362.

## Linked entities

- **Diseases:** pancreatic cancer (MONDO:0005192)

## Full-text entities

- **Diseases:** pancreatic cancer (MESH:D010190), cancers (MESH:D009369), PPH (MESH:D020206), POPF (MESH:D010185), hemorrhage (MESH:D006470)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12341475/full.md

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Source: https://tomesphere.com/paper/PMC12341475