Association Between Vonoprazan and the Risk of Gastric Cancer After Helicobacter pylori Eradication

被引:5
|
作者
Arai, Junya [1 ,2 ]
Miyawaki, Atsushi [3 ]
Aoki, Tomonori [2 ]
Niikura, Ryota [4 ]
Hayakawa, Yoku [2 ]
Fujiwara, Hiroaki [1 ]
Ihara, Sozaburo [2 ]
Fujishiro, Mitsuhiro [2 ]
Kasuga, Masato [5 ]
机构
[1] Asahi Life Fdn, Inst Med Sci, Div Gastroenterol, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Gastroenterol, Bunkyo Ku, Hongo, Tokyo 1138655, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Hlth Serv Res, Tokyo, Japan
[4] Tokyo Med Univ, Grad Sch Med, Dept Endoscopy, Shinjuku Ku, Tokyo, Tokyo 1608402, Japan
[5] Asahi Life Fdn, Inst Med Sci, Tokyo, Japan
关键词
Gastric Cancer; Helicobacter pylori; Potassium-Competitive Acid Blocker; Proton Pump Inhibitor; PROTON-PUMP INHIBITORS; THERAPY; COHORT;
D O I
10.1016/j.cgh.2024.01.037
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Potassium -competitive acid blockers (PCABs) have been increasingly used to treat upper gastrointestinal disorders, replacing proton pump inhibitors (PPIs). Whereas PPIs are associated with an increased risk of gastric cancer (GC) after Helicobacter pylori (Hp) eradication, it is uncertain whether PCABs carry the same risk. METHODS: Using a population -based claims database in Japan, we identi fi ed patients who were prescribed a clarithromycin-based fi rst regimen of Hp eradication between 2015 and 2018. Patients who failed this regimen and those diagnosed with GC before or within 1 year after Hp eradication were excluded. We compared GC incidence between PCAB users and histamine type -2 receptor antagonist (H2RA) users, matching them on the basis of propensity scores calculated with considerations for age, sex, smoking, alcohol consumption, comorbidities, and co -administered medications. PCABs included only vonoprazan in this study. RESULTS: Among 54,055 patients, 568 (1.05%) developed GC during the follow-up period (mean, 3.65 years). The cumulative incidence of GC was 1.64% at 3 years, 2.02% at 4 years, and 2.36% at 5 years in PCAB users and 0.71% at 3 years, 1.04% at 4 years, and 1.22% at 5 years in H2RA users. The use of PCABs was associated with a higher GC risk (matched hazard ratio, 1.92; 95% con fi dence interval, 1.13 - 3.25; P [ .016). Longer PCAB use and high -dose PCAB use were signi fi cantly associated with higher incidence of GC. Sensitivity analyses showed the risk of GC incidence among PCAB users was comparable with that of PPI users. CONCLUSIONS: The use of PCABs was associated with an increased risk of GC among Hp -eradicated patients, with duration/dose response effects.
引用
收藏
页码:1217 / 1225.e6
页数:15
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