# Comparative effectiveness and safety of vonoprazan/amoxicillin-based dual therapy versus quadruple therapy as second-line treatment for Helicobacter pylori Infection: a retrospective cohort study

**Authors:** Ying-Ying Han, Ji-Yan Li, Ya-Ni Zhou, Lin Tuo, Ge Wang, Jing-Mei Liu, Zhen-Zhen Zhou, Mei Liu, Pei-Yuan Li

PMC · DOI: 10.1007/s10238-025-02037-8 · Clinical and Experimental Medicine · 2026-01-20

## TL;DR

This study compares two second-line treatments for Helicobacter pylori infection and finds that a simpler dual therapy is as effective as a more complex one but with fewer side effects.

## Contribution

The study introduces a simplified dual therapy as a viable second-line treatment for H. pylori with comparable efficacy and better safety than quadruple therapy.

## Key findings

- VA dual therapy and VAMB quadruple therapy had comparable eradication rates in second-line treatment.
- VA therapy had significantly fewer adverse events compared to VAMB therapy.
- Both treatment groups showed excellent medication adherence.

## Abstract

The introduction of vonoprazan has markedly enhanced the effectiveness of the first-line Helicobacter pylori (H. pylori) eradication regimens. This study aimed to compare the effectiveness of vonoprazan-amoxicillin based dual therapy with that of quadruple therapy as second-line treatments, while also investigating potential clinical predictors of therapeutic success. From January 2023 to June 2025, we retrospectively analyzed clinical data from H. pylori-infected patients who received second-line treatment with either: vonoprazan-amoxicillin dual therapy (VA) or VA based quadruple therapy (VAMB; vonoprazan, amoxicillin, minocycline, and colloidal bismuth pectin). The eradication status was evaluated by 13/14C­urease breath test four weeks after treatment completion. Adverse events and medication compliance were systematically documented during follow-up. The study included 241 patients, with 107 receiving VA dual therapy and 134 undergoing VAMB quadruple therapy. Eradication rates were comparable between groups: 90.7% (VA) versus 92.5% (VAMB) by modified intention-to-treat (mITT) analysis, and 91.4% versus 93.7% by per-protocol (PP) analysis (all p > 0.05). Notably, the VA regimen demonstrated significantly fewer adverse events (8.4% vs 17.9%, p = 0.033). Both treatment arms maintained excellent medication adherence. Compared to the vonoprazan-amoxicillin-minocycline-bismuth (VAMB) quadruple regimen, vonoprazan-amoxicillin (VA) dual therapy achieved comparable eradication efficacy with a more favorable safety profile in second-line H. pylori treatment, representing a simplified yet effective rescue therapy option.

## Linked entities

- **Chemicals:** vonoprazan (PubChem CID 15981397), amoxicillin (PubChem CID 33613), minocycline (PubChem CID 54675783)

## Full-text entities

- **Diseases:** infected (MESH:D007239), nausea/vomiting (MESH:D020250), Dizziness (MESH:D004244), Nausea (MESH:D009325), mITT (MESH:D014202), rashes (MESH:D005076), gastric and extra-gastric complications (MESH:D013272), diarrhea (MESH:D003967), abdominal pain (MESH:D015746), abdominal distension (MESH:D000007), H. pylori infection (MESH:D016481), Vomiting (MESH:D014839), gastric cancer (MESH:D013274)
- **Chemicals:** rabeprazole (MESH:D064750), bismuth (MESH:D001729), amoxicillin (MESH:D000658), fluoroquinolone (MESH:D024841), esomeprazole (MESH:D064098), 14C-UBT (-), vonoprazan (MESH:C552956), metronidazole (MESH:D008795), lipid (MESH:D008055), alcohol (MESH:D000438), tetracycline (MESH:D013752), urea (MESH:D014508), clarithromycin (MESH:D017291), levofloxacin (MESH:D064704), tetracyclines (MESH:D013754), furazolidone (MESH:D005664), minocycline (MESH:D008911)
- **Species:** Homo sapiens (human, species) [taxon 9606], Helicobacter pylori (species) [taxon 210]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12847212