Dual Therapy with Vonoprazan and Amoxicillin Is as Effective as Triple Therapy with Vonoprazan, Amoxicillin and Clarithromycin for Eradication of Helicobacter pylori.


Journal

Digestion
ISSN: 1421-9867
Titre abrégé: Digestion
Pays: Switzerland
ID NLM: 0150472

Informations de publication

Date de publication:
2020
Historique:
received: 06 06 2019
accepted: 23 07 2019
pubmed: 23 8 2019
medline: 31 7 2021
entrez: 22 8 2019
Statut: ppublish

Résumé

Vonoprazan (VPZ) is the first clinically available potassium competitive acid blocker. This class of agents provides faster and more potent acid inhibition than proton pump inhibitors. Most strains of Helicobacter pylori are sensitive to amoxicillin. We hypothesized that dual therapy with VPZ and amoxicillin would provide the sufficient eradication rate for H. pylori infection. To evaluate this, we compared the eradication rate by the dual VPZ/amoxicillin therapy with that by the standard triple VPZ/amoxicillin/clarithromycin therapy. Non-inferiority of the eradication rate of H. pylori by the dual therapy with VPZ 20 mg twice daily (bid) and amoxicillin 500 mg 3 times daily (tid) for 1 week to that by the triple therapy with VPZ 20 mg bid, amoxicillin 750 mg bid and clarithromycin 200 mg bid for 1 week was retrospectively studied. Propensity score matching was performed to improve comparability between 2 regimen groups. Successful eradication was diagnosed using the [13C]-urea breath test at 1-2 months after the end of eradication therapy. The intention-to-treat analysis demonstrated that the eradication rate by the dual therapy (92.9%; 95% CI 82.7-98.0%, 52/56) was not inferior to that of the triple therapy (91.9%; 95% CI 80.4-97.0%, 51/56; OR 1.275, 95% CI 0.324-5.017%, p = 0.728). There were no statistically significant differences in incidences of adverse events between 2 regimens. VPZ-based dual therapy (VPZ 20 mg bid and amoxicillin 500 mg tid for 1 week) provides an acceptable eradication rate of H. pylori infection without the need for second antimicrobial agents, such as clarithromycin.

Sections du résumé

BACKGROUNDS/AIMS OBJECTIVE
Vonoprazan (VPZ) is the first clinically available potassium competitive acid blocker. This class of agents provides faster and more potent acid inhibition than proton pump inhibitors. Most strains of Helicobacter pylori are sensitive to amoxicillin. We hypothesized that dual therapy with VPZ and amoxicillin would provide the sufficient eradication rate for H. pylori infection. To evaluate this, we compared the eradication rate by the dual VPZ/amoxicillin therapy with that by the standard triple VPZ/amoxicillin/clarithromycin therapy.
METHODS METHODS
Non-inferiority of the eradication rate of H. pylori by the dual therapy with VPZ 20 mg twice daily (bid) and amoxicillin 500 mg 3 times daily (tid) for 1 week to that by the triple therapy with VPZ 20 mg bid, amoxicillin 750 mg bid and clarithromycin 200 mg bid for 1 week was retrospectively studied. Propensity score matching was performed to improve comparability between 2 regimen groups. Successful eradication was diagnosed using the [13C]-urea breath test at 1-2 months after the end of eradication therapy.
RESULTS RESULTS
The intention-to-treat analysis demonstrated that the eradication rate by the dual therapy (92.9%; 95% CI 82.7-98.0%, 52/56) was not inferior to that of the triple therapy (91.9%; 95% CI 80.4-97.0%, 51/56; OR 1.275, 95% CI 0.324-5.017%, p = 0.728). There were no statistically significant differences in incidences of adverse events between 2 regimens.
CONCLUSION CONCLUSIONS
VPZ-based dual therapy (VPZ 20 mg bid and amoxicillin 500 mg tid for 1 week) provides an acceptable eradication rate of H. pylori infection without the need for second antimicrobial agents, such as clarithromycin.

Identifiants

pubmed: 31434101
pii: 000502287
doi: 10.1159/000502287
doi:

Substances chimiques

1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine 0
Anti-Bacterial Agents 0
Proton Pump Inhibitors 0
Pyrroles 0
Sulfonamides 0
Amoxicillin 804826J2HU
Clarithromycin H1250JIK0A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

743-751

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Takahisa Furuta (T)

Center for Clinical Research, Hamamatsu University School of Medicine, Hamamatsu, Japan, furuta@hama-med.ac.jp.

Mihoko Yamade (M)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Takuma Kagami (T)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Takahiro Uotani (T)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Takahiro Suzuki (T)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Tomohiro Higuchi (T)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Shinya Tani (S)

Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Yasushi Hamaya (Y)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Moriya Iwaizumi (M)

Department of Laboratory Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Hiroaki Miyajima (H)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Kazuo Umemura (K)

Center for Clinical Research, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Department of Pharmacology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Satoshi Osawa (S)

Department of Endoscopic and Photodynamic Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Ken Sugimoto (K)

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

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Classifications MeSH