# The influence of concomitant proton pump inhibitors use on treatment efficacy in hepatocellular carcinoma patients receiving immune checkpoint inhibitors: a systematic review and meta-analysis

**Authors:** Yangfei Duan, Qitai Zhao, Shumin Feng, Wei Jing, Dan Wang, Yi Zhang

PMC · DOI: 10.3389/fimmu.2026.1717420 · 2026-02-03

## TL;DR

This study examines whether proton pump inhibitors affect the effectiveness of cancer immunotherapy in liver cancer patients.

## Contribution

A meta-analysis evaluating the clinical impact of proton pump inhibitors in hepatocellular carcinoma patients receiving immunotherapy.

## Key findings

- No significant association found between PPIs use and overall survival in HCC patients receiving ICIs.
- No significant association found between PPIs use and progression-free survival in HCC patients receiving ICIs.

## Abstract

Despite the significant survival benefit offered by immune checkpoint inhibitors (ICIs) in patients with hepatocellular carcinoma (HCC), a subset of patients still develop drug resistance. Recent evidence suggests that proton pump inhibitors (PPIs) may influence the therapeutic efficacy of ICIs, but the clinical relevance of this interaction remains unclear. This meta-analysis aims to systematically evaluate the association between concomitant PPIs use and clinical outcomes in HCC patients receiving ICIs therapy.

A comprehensive search of the PubMed, Embase (via Ovid), and Web of Science databases was conducted to identify relevant studies published before May 14, 2025. The primary endpoints of the meta-analysis were overall survival (OS) and progression-free survival (PFS).

Five retrospective studies comprising a total of 1,257 patients were included, of whom 606 (48.2%) received PPIs concurrently with ICIs. The meta-analysis showed no statistically significant association between PPIs use and either OS (HR: 1.04, 95% CI: 0.88-1.24, P = 0.64) or PFS (HR: 0.92, 95% CI: 0.74-1.14, P = 0.44). These findings were further supported by a Bayesian sensitivity analysis performed to address the uncertainty inherent in a limited number of studies.

Based on the current evidence from retrospective studies, concomitant use of PPIs does not appear to significantly affect survival outcomes in HCC patients treated with ICIs. However, given the inherent limitations of the included studies, this conclusion should be interpreted with caution and warrants validation through prospective investigations.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251026028, CRD420251026028.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), liver cancer (MONDO:0002691)

## Full-text entities

- **Genes:** CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 397286], PDCD1 (programmed cell death 1) [NCBI Gene 100533201], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, AFP (alpha fetoprotein) [NCBI Gene 397586], CD274 (CD274 molecule) [NCBI Gene 574058] {aka PDL1}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** cancer (MESH:D009369), inflammatory (MESH:D007249), chronic liver disease (MESH:D008107), gastroesophageal reflux disease (MESH:D005764), cirrhosis (MESH:D005355), NSCLC (MESH:D002289), ulcer (MESH:D014456), death (MESH:D003643), UC (MESH:D014523), viral hepatitis (MESH:D014777), OS (MESH:D011475), Barcelona Clinic Liver Cancer (MESH:D006528)
- **Chemicals:** Bevacizumab (MESH:D000068258), Atezolizumab (MESH:C000594389), Atez (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960652/full.md

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Source: https://tomesphere.com/paper/PMC12960652