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Introduction: No study has investigated the efficacy and safety of vonoprazan-amoxicillin dual therapy compared with bismuth quadruple therapy (B-quadruple). This study aimed to evaluate the efficacy and safety of 10-day vonoprazan-amoxicillin dual therapy as a first-line treatment of Helicobacter pylori infection compared with B-quadruple and to explore the optimal dosage of amoxicillin in the dual therapy.
Methods: A total of 375 treatment-naive, H. pylori -infected subjects were randomly assigned in a 1:1:1 ratio into 3 regimen groups including VHA-dual (vonoprazan 20 mg twice/day + amoxicillin 750 mg 4 times/day), VA-dual (vonoprazan 20 mg + amoxicillin 1,000 mg twice/day), and B-quadruple (esomeprazole 20 mg + bismuth 200 mg + amoxicillin 1,000 mg + clarithromycin 500 mg twice/day). Eradication rates, adverse events (AEs), and compliance were compared between 3 groups.
Results: The eradication rates of B-quadruple, VHA-dual, and VA-dual were 90.9%, 93.4%, and 85.1%, respectively, by per-protocol analysis; 89.4%, 92.7%, and 84.4%, respectively, by modified intention-to-treat analysis; 88.0%, 91.2%, and 82.4%, respectively, by intention-to-treat analysis. The efficacy of the VHA-dual group was not inferior to the B-quadruple group ( P < 0.001), but VA-dual did not reach a noninferiority margin of -10%. The AEs rates of the B-quadruple group were significantly higher than those of the VHA-dual ( P = 0.012) and VA-dual ( P = 0.001) groups. There was no significant difference in medication compliance among 3 treatment groups ( P = 0.995).
Conclusions: The 10-day VHA-dual therapy provided satisfactory eradication rates of >90%, lower AEs rates, and similar adherence compared with B-quadruple therapy as a first-line therapy for H. pylori infection. However, the efficacy of VA-dual therapy was not acceptable.
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http://dx.doi.org/10.14309/ajg.0000000000002086 | DOI Listing |
Medicine (Baltimore)
August 2025
Department of Gastroenterology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
This study aims to evaluate the efficacy of vonoprazan combined with amoxicillin (vonoprazan-amoxicillin [VA]) at the same dose but different administration frequencies in treating Helicobacter pylori (Helicobacter pylori [Hp]) infection. This retrospective study analyzed 236 Hp-positive patients. Patients were treated with the VA regimen for 14 days and divided based on amoxicillin administration frequency: L-VA: vonoprazan 20 mg bid + amoxicillin 1 g tid; H-VA: vonoprazan 20 mg bid + amoxicillin 0.
View Article and Find Full Text PDFHelicobacter
August 2025
Department of Gastroenterology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiansgsu, China.
Background: A 10 day vonoprazan-amoxicillin (VA) regimen (amoxicillin 750 mg four times daily) achieved > 90% Helicobacter pylori (H. pylori) eradication rates in the initial treatment. Whether less frequent dosing or shorter duration provides comparable efficacy remains unclear.
View Article and Find Full Text PDFTherap Adv Gastroenterol
July 2025
The School of Clinical Medicine, Fujian Medical University, No. 88 Jiaotong Road, Fuzhou 350004, Fujian, China.
Background: Potassium-competitive acid blockers (P-CABs) have shown potential in () eradication, but the efficacy of dual therapy with P-CABs and amoxicillin remains underexplored.
Objectives: This study evaluated the efficacy, safety, and compliance of a 14-day vonoprazan-amoxicillin (VA) dual therapy compared to a bismuth-based quadruple therapy (BQT) in treatment-naive patients.
Design: A randomized clinical trial.
Helicobacter
June 2025
Department of Gastroenterology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu, China.
Background: Limited research has explored the efficacy of reduced amoxicillin dosages in vonoprazan-amoxicillin (VA) dual therapy for Helicobacter pylori eradication in China, and this study aimed to assess the noninferiority of these lower dosages compared to the standard high dose (3 g/d).
Methods: This was a noninferiority study with a -10% margin. H.
World J Gastroenterol
April 2025
Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha 410013, Hunan Province, China.
Background: Effective acid suppression significantly enhances the eradication rate of ().
Aim: To assess the efficacy and safety of high-dose dual therapy (HDDT) utilizing various highly potent antisecretory medications, thereby providing additional clinical guidance for eradication.
Methods: The study population comprised untreated patients from three medical centers in central China.