Vonoprazan Versus Proton-Pump Inhibitors for the Management of Severe Reflux Esophagitis: A Systematic Review and Network Meta-Analysis

Author(s)

Zhang X1, Yan B1, Sai X1, Sheng Y2, Peng L1, Yang Y1
1Chinese PLA General Hospital, Beijing, China, 2Takeda China Inc., Beijing, China

OBJECTIVES : Reflux esophagitis (RE) is an esophageal mucosal injury that occurs secondary to the regurgitation of stomach contents. An 8-week course of proton pump inhibitors (PPIs) has been the mainstay for the management of RE. Vonoprazan, a novel potassium-competitive acid blocking agent, demonstrated strong, fast and long-lasting acid inhibitory effects in patients with RE of any grades. In this study, We conducted a network meta-analysis (NMA) to assess the efficacy of 4-week vonoprazan and 8-week PPIs in severe RE.

METHODS : Medline, EMBASE and Cochrane Central Register of Controlled Trials were searched up to April 20, 2020, aiming for publications of randomized controlled trials reporting healing rates of vonoprazan 20mg at 4 weeks and PPIs (esomeprazole, ilaprazole, lansoprazole, omeprazole, pantoprazole, rabeprazole) in approved doses at 8 weeks among adults with severe RE. Bayesian NMAs with random-effect models were performed to compare each PPI versus vonoprazan. Odds ratios (ORs) and 95% credible intervals (CrIs) were reported. Between-study heterogeneity and consistency were evaluated.

RESULTS : Among 2,546 articles identified, 12 studies were selected into the NMA, which include 3 articles with vonoprazan and 9 articles with PPIs. Among patients with severe RE, the efficacy of 4-week vonoprazan was comparable to 8-week PPIs. Specifically, the ORs (CrIs)of PPIs vs. vonoprazan 20mg among patients with severe RE were as follows: esomeprazole 20mg 1.22 (0.51-3.01), esomeprazole 40mg 1.47 (0.76-2.86), lansoprazole 30mg 0.82 (0.44-1.56), omeprazole 20mg 0.90 (0.43-1.89), omeprazole 40mg 0.35 (0.04-2.09), pantoprazole 40mg 1.87 (0.50-7.35) and rabeprazole 20mg 1.06 (0.22-6.32). Ilaprazole was not included in the NMA due to lack of evidence in patients with severe RE. Heterogeneity existed in few comparisons and there was no evidence of inconsistency.

CONCLUSIONS : This NMA suggested that a 4-week course of vonoprazan had comparable efficacy to 8-week course of PPIs for patients with severe RE.

Conference/Value in Health Info

2021-05, ISPOR 2021, Montreal, Canada

Value in Health, Volume 24, Issue 5, S1 (May 2021)

Code

PGI1

Topic

Clinical Outcomes

Topic Subcategory

Clinical Outcomes Assessment, Comparative Effectiveness or Efficacy

Disease

Gastrointestinal Disorders

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