Vonoprazan Triple and Dual Therapy
for Helicobacter pylori Infection in
the United States and Europe:
Randomized Clinical Trial
Gastroenterology 2022;163:3
Published on 6 June 2022
MODERATOR: Dr. K Romeo Singh
PRESENTER: Dr. P Kireeti
INTRODUCTION
• H. pylori is a leading cause of peptic ulcer, gastric
adenocarcinoma, gastric MALT lymphoma
• Treatment is by PPI based antibiotic therapy
• Eradication rates dropped to <80%, mainly due to
clarithromycin resistance
• Antibiotic action is influenced by intragastric pH, so
sustained control of pH may improve eradication rates
OBJECTIVE
• To evaluate the efficacy of vonoprazan, a
potassium-competitive acid blocker, vs
standard treatment on H pylori eradication in
the United States and Europe.
METHODS
• STUDY DESIGN : randomized controlled, phase 3 trial
• STUDY SETTING: multiple sites in the US and
Europe
• STUDY DURATION :2 yrs, Dec 2019 to Feb 2022
• SAMPLE SIZE: 1046 , 349- vonoprazan triple therapy,
349- vonoprazan dual, 348- lansoprazole triple therapy
INCLUSION CRITERIA
• ≥18 years old and had at least 1 of the following :
• dyspepsia;
• a recent/new diagnosis of non bleeding peptic ulcer;
• history of peptic ulcer not previously treated for H pylori
infection; H pylori infection diagnosed with a positive
13C-urea breath test (UBT)
EXCLUSION CRITERIA
• Patients with
• gastric cancer,
• gastric or duodenal ulcer with current or recent
bleeding,
• GI bleeding within 4 weeks of randomization
PROCEDURE
• Patients were randomly assigned 1:1:1 to
• Vonoprazan dual therapy (vonoprazan 20 mg BD and
amoxicillin 1 g TDS),
• Triple therapy with either vonoprazan 20 mg twice daily,
or lansoprazole 30 mg BD, each given with amoxicillin 1
g BD, and clarithromycin 500 mg BD for 14 days.
• H pylori status was assessed by 13C-UBT at week 6
OUTCOMES
• PRIMARY OUTCOME
• Noninferiority in eradication rates in patients
without clarithromycin- and amoxicillin-resistant
strains
• SECONDARY OUTCOME
• Superiority in eradication rates in clarithromycin-
resistant infections
STATISTICAL ANALYSIS
• Farrington and Manning test with a non inferiority
margin of 10% for the primary and secondary outcomes
• All statistical tests were 2-sided, with 95% CI and a
significance level of 0.05 (P value)
• Statistical analyses were performed using SAS for
Windows, version 9.4
RESULTS
• Primary outcome – eradication rates in non
resistant strains
• Vonoprazan triple therapy -84.7%
• Lansoprazole dual therapy-78.5%
• Lansoprazole triple therapy-78.8%
• Secondary outcome-eradication rates in resistant
strains strains
• Vonoprazan triple therapy - 65.8%
• Lansoprazole dual therapy- 69.6%
• Lansoprazole triple therapy-31.9%
• Frequency of TEAEs was similar between
vonoprazan and lansoprazole regimens
LIMITATIONS
• Previously treated pts are not included
• Study sites were not evenly distributed geographically
across the US and included only 5 European countries,
thus limiting generalizability to other geographic
regions
• The data were not adjusted for biases associated with
multiple sites
DISCUSSION
• Vonoprazan is a potassium-competitive acid blocker,
currently approved for the treatment of H pylori
infection and other acid-related diseases in several
countries. It ↑ intragastric pH rapidly and potently and
maintains it to a greater degree than PPIs; this has been
associated with higher H pylori eradication rates
• Optimizing current regimens offers the potential to
increase eradication rates and reduce additional antibiotic
usage, thereby promoting and improving antimicrobial
stewardship
• Vonoprazan therapy had the higher eradication rate and a
greater therapeutic gain over lansoprazole therapy
• All regimens were generally well tolerated. Most TEAEs
were mild to moderate in severity. Serious TEAEs were
uncommon and none was considered related to study
drugs.
CONCLUSION
• Vonoprazan-based triple and dual regimens were
noninferior and to lansoprazole-based triple therapy
for eradication of H pylori infection
THANK YOU

vono.pptx

  • 1.
    Vonoprazan Triple andDual Therapy for Helicobacter pylori Infection in the United States and Europe: Randomized Clinical Trial Gastroenterology 2022;163:3 Published on 6 June 2022 MODERATOR: Dr. K Romeo Singh PRESENTER: Dr. P Kireeti
  • 2.
    INTRODUCTION • H. pyloriis a leading cause of peptic ulcer, gastric adenocarcinoma, gastric MALT lymphoma • Treatment is by PPI based antibiotic therapy • Eradication rates dropped to <80%, mainly due to clarithromycin resistance • Antibiotic action is influenced by intragastric pH, so sustained control of pH may improve eradication rates
  • 3.
    OBJECTIVE • To evaluatethe efficacy of vonoprazan, a potassium-competitive acid blocker, vs standard treatment on H pylori eradication in the United States and Europe.
  • 4.
    METHODS • STUDY DESIGN: randomized controlled, phase 3 trial • STUDY SETTING: multiple sites in the US and Europe • STUDY DURATION :2 yrs, Dec 2019 to Feb 2022 • SAMPLE SIZE: 1046 , 349- vonoprazan triple therapy, 349- vonoprazan dual, 348- lansoprazole triple therapy
  • 5.
    INCLUSION CRITERIA • ≥18years old and had at least 1 of the following : • dyspepsia; • a recent/new diagnosis of non bleeding peptic ulcer; • history of peptic ulcer not previously treated for H pylori infection; H pylori infection diagnosed with a positive 13C-urea breath test (UBT)
  • 6.
    EXCLUSION CRITERIA • Patientswith • gastric cancer, • gastric or duodenal ulcer with current or recent bleeding, • GI bleeding within 4 weeks of randomization
  • 7.
    PROCEDURE • Patients wererandomly assigned 1:1:1 to • Vonoprazan dual therapy (vonoprazan 20 mg BD and amoxicillin 1 g TDS), • Triple therapy with either vonoprazan 20 mg twice daily, or lansoprazole 30 mg BD, each given with amoxicillin 1 g BD, and clarithromycin 500 mg BD for 14 days. • H pylori status was assessed by 13C-UBT at week 6
  • 10.
    OUTCOMES • PRIMARY OUTCOME •Noninferiority in eradication rates in patients without clarithromycin- and amoxicillin-resistant strains • SECONDARY OUTCOME • Superiority in eradication rates in clarithromycin- resistant infections
  • 11.
    STATISTICAL ANALYSIS • Farringtonand Manning test with a non inferiority margin of 10% for the primary and secondary outcomes • All statistical tests were 2-sided, with 95% CI and a significance level of 0.05 (P value) • Statistical analyses were performed using SAS for Windows, version 9.4
  • 12.
    RESULTS • Primary outcome– eradication rates in non resistant strains • Vonoprazan triple therapy -84.7% • Lansoprazole dual therapy-78.5% • Lansoprazole triple therapy-78.8% • Secondary outcome-eradication rates in resistant strains strains • Vonoprazan triple therapy - 65.8% • Lansoprazole dual therapy- 69.6% • Lansoprazole triple therapy-31.9% • Frequency of TEAEs was similar between vonoprazan and lansoprazole regimens
  • 16.
    LIMITATIONS • Previously treatedpts are not included • Study sites were not evenly distributed geographically across the US and included only 5 European countries, thus limiting generalizability to other geographic regions • The data were not adjusted for biases associated with multiple sites
  • 18.
    DISCUSSION • Vonoprazan isa potassium-competitive acid blocker, currently approved for the treatment of H pylori infection and other acid-related diseases in several countries. It ↑ intragastric pH rapidly and potently and maintains it to a greater degree than PPIs; this has been associated with higher H pylori eradication rates
  • 19.
    • Optimizing currentregimens offers the potential to increase eradication rates and reduce additional antibiotic usage, thereby promoting and improving antimicrobial stewardship • Vonoprazan therapy had the higher eradication rate and a greater therapeutic gain over lansoprazole therapy • All regimens were generally well tolerated. Most TEAEs were mild to moderate in severity. Serious TEAEs were uncommon and none was considered related to study drugs.
  • 20.
    CONCLUSION • Vonoprazan-based tripleand dual regimens were noninferior and to lansoprazole-based triple therapy for eradication of H pylori infection
  • 21.