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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Gastroenterol. Jan 21, 2027; 33(3): 127331
Published online Jan 21, 2027. doi: 10.3748/wjg.127331
Randomized trial of vonoprazan dual therapy vs bismuth-containing quadruple therapy with two low-resistance antibiotics for Helicobacter pylori eradication
Jian-Hong Chen, Xiao-Wen Liu, Yan-Ting Xu, Ning Wang, Jun-Feng Guo, Lu-Yang Chen, Fu-Sheng Gao, Chuan Zhang
Jian-Hong Chen, Xiao-Wen Liu, Yan-Ting Xu, Ning Wang, Jun-Feng Guo, Lu-Yang Chen, Fu-Sheng Gao, Chuan Zhang, Department of Gastroenterology, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
Co-corresponding authors: Fu-Sheng Gao and Chuan Zhang.
Author contributions: Chen JH, Zhang C, and Gao FS designed this study; Chen JH, Liu XW, Xu YT, Wang N, Guo JF and Chen LY screened patients and acquired clinical data. Chen JH, Gao FS, and Zhang C performed data analysis and interpretation; Chen JH drafted the manuscript. All the authors have read and approved the final manuscript. Zhang C and Gao FS have played important roles in the study design and data analysis as the co-corresponding authors. Zhang C and Gao FS conceived, designed, and supervised the study, and performed data analysis and interpretation.
AI contribution statement: Portions of this manuscript were edited using AI tools solely for language refinement. The authors carefully reviewed and verified all AI-assisted outputs and take full responsibility for the scientific content of the manuscript.
Supported by the National Natural Science Foundation of China, No. 81900505; and Beijing Municipal Administration of Hospitals’ Youth Program, No. QML20200702.
Institutional review board statement: The study protocol received ethical approval from the independent Ethics Committee of Beijing Tongren Hospital (Approval No. TREC2025-KY070).
Clinical trial registration statement: This study is registered at https://www.chictr.org.cn/showprojEN.html?proj=278033. The registration identification number is ChiCTR2500105014.
Informed consent statement: All study participants provided informed written consent prior to study enrollment.
Conflict-of-interest statement: The authors declare that they have no conflict of interest.
CONSORT 2010 statement: The authors have read the CONSORT 2010 Statement, and the manuscript was prepared and revised according to the CONSORT 2010 Statement.
Data sharing statement: De-identified participant-level data, statistical code, and the data dictionary used in this study are available from the corresponding author upon reasonable request, subject to institutional and ethical approvals.
Corresponding author: Chuan Zhang, MD, Department of Gastroenterology, Beijing Tongren Hospital, Capital Medical University, No. 1 Dongjiaomin Lane, Dongcheng District, Beijing 100730, China. digestivezhang@163.com
Received: August 28, 2026
Revised: September 20, 2026
Accepted: November 4, 2026
Published online: January 21, 2027
Processing time: 78 Days and 15 Hours
Abstract
BACKGROUND

Given the escalating resistance rates to commonly used antibiotics in Helicobacter pylori (H. pylori) eradication, regimens containing two antibiotics with low resistance rates were increasingly used in clinical practice to maximize successful initial eradication.

AIM

To compare the efficacy and safety of vonoprazan-amoxicillin (VA) dual therapy and vonoprazan-based bismuth-containing quadruple therapy with two low-resistance antibiotics (amoxicillin and minocycline) in treatment-naïve H. pylori infection.

METHODS

A total of 184 treatment‐naïve H. pylori-infected patients were randomly assigned to receive either VA (vonoprazan fumarate 20 mg twice daily and amoxicillin 1000 mg three times daily) or VBAM (vonoprazan fumarate 20 mg twice daily, bismuth potassium citrate 240 mg twice daily, amoxicillin 1000 mg twice daily, and minocycline hydrochloride 100 mg twice daily) for 14 days. Adverse events and medication adherence were recorded during follow‐up. H. pylori eradication was assessed by a 13C- or 14C-urea breath test 4 weeks after treatment completion.

RESULTS

Eradication rates were 92.4% (85/92, 95%CI: 85.1%-96.3%) for VA and 91.3% (84/92, 95%CI: 83.8%-95.5%) for VBAM by intention‐to‐treat analysis (difference 1.1%; 95%CI: -6.8% to 9.0%; non-inferiority P = 0.003); 95.5% (85/89, 95%CI: 89.0%-98.2%) and 96.6% (84/87, 95%CI: 90.4%-98.8%) by modified intention‐to‐treat analysis (difference -1.1%; 95%CI: -6.8% to 4.7%; non-inferiority P = 0.001); 95.4% (83/87, 95%CI: 88.8%-98.2%) and 96.4% (81/84, 95%CI: 90.0%-98.8%) by per‐protocol analysis (difference -1.0%; 95%CI: -7.0% to 4.9%; non-inferiority P = 0.002). In all three analysis sets, the lower limits of the 95%CI for the rate difference were above the prespecified non-inferiority margin of -10%. No significant differences were observed between the two groups in overall adverse event incidence or adherence, but the incidence of dizziness was lower in the VA group (1.1% vs 9.8%, P = 0.023). The incremental cost-effectiveness ratio for VA vs VBAM was -15958.18 CNY per additional successfully eradicated patient from a healthcare payer perspective.

CONCLUSION

The VA dual regimen is non‐inferior to the VBAM quadruple therapy in eradication rate for treatment‐naïve H. pylori infection, while being associated with fewer dizziness events and lower direct medical costs from a healthcare payer perspective.

Keywords: Helicobacter pylori; Vonoprazan; Amoxicillin; Minocycline; Eradication; Safety; Randomized controlled trial

Core Tip: This single-center, open-label randomized trial compared vonoprazan-amoxicillin (VA) dual therapy with vonoprazan-based bismuth-containing quadruple therapy containing amoxicillin and minocycline (VBAM) in treatment-naïve Helicobacter pylori infection. VA was non-inferior to VBAM in eradication rates across all analysis sets. Overall adverse events were comparable, but VA had fewer dizziness events. From a healthcare payer perspective, VA had lower direct medical costs. However, the generalizability of these findings to broader populations and different resistance patterns requires further investigation.

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