Vonoprazan is noninferior to proton pump inhibitors in bismuth-containing quadruple therapy for the treatment of Helicobacter pylori infection : A propensity score matching analysis
© 2023 Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd..
OBJECTIVE: This study aimed to evaluate the efficacy and safety of vonoprazan (VPZ) versus proton pump inhibitor (PPI) in clarithromycin-based bismuth-containing quadruple therapy (C-BQT) for the treatment of Helicobacter pylori (H. pylori) eradication.
METHODS: Medical records of patients in whom H. pylori was eradicated between 1 July 2018 and 31 December 2021 were retrieved retrospectively from the Outpatient Unit of Qilu Hospital. Efficacy, safety, and compliance were compared between VPZ-based and PPI-based C-BQT, containing vonoprazan 20 mg or proton pump inhibitors (lansoprazole 30 mg or esomeprazole 20 mg), bismuth 220 or 200 mg, amoxicillin 1000 mg, and clarithromycin 500 mg, twice daily for 2 weeks by 1:1 propensity score matching analysis. The trial was registed on ClinicalTrials.gov (registration no. NCT05301725).
RESULTS: The H. pylori eradication rates of VPZ-based and PPI-based therapies were 88.8% (151/170) and 87.6% (149/170) in the intention-to-treat analysis, 94.1% (144/153) and 91.1% (144/158) in the per-protocol analysis, respectively. The noninferiority of VPZ to PPI was confirmed in all analyses (P < 0.001). The incidence of adverse events was 30.0% (51/170) and 27.1% (46/170) in the VPZ-based and PPI-based groups, respectively. VPZ-based and PPI-based therapies were well tolerated and showed good patient compliance without significant differences.
CONCLUSIONS: VPZ-based therapy resulted in a satisfactory eradication rate and was well tolerated for H. pylori eradication, which are comparable to PPIs in C-BQT as a first-line treatment for H. pylori infection.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:24 |
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Enthalten in: |
Journal of digestive diseases - 24(2023), 1 vom: 01. Jan., Seite 19-27 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Wang, Juan [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 07.05.2023 Date Revised 07.05.2023 published: Print-Electronic ClinicalTrials.gov: NCT05301725 Citation Status MEDLINE |
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doi: |
10.1111/1751-2980.13166 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM354656910 |
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245 | 1 | 0 | |a Vonoprazan is noninferior to proton pump inhibitors in bismuth-containing quadruple therapy for the treatment of Helicobacter pylori infection |b A propensity score matching analysis |
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500 | |a ClinicalTrials.gov: NCT05301725 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023 Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd. | ||
520 | |a OBJECTIVE: This study aimed to evaluate the efficacy and safety of vonoprazan (VPZ) versus proton pump inhibitor (PPI) in clarithromycin-based bismuth-containing quadruple therapy (C-BQT) for the treatment of Helicobacter pylori (H. pylori) eradication | ||
520 | |a METHODS: Medical records of patients in whom H. pylori was eradicated between 1 July 2018 and 31 December 2021 were retrieved retrospectively from the Outpatient Unit of Qilu Hospital. Efficacy, safety, and compliance were compared between VPZ-based and PPI-based C-BQT, containing vonoprazan 20 mg or proton pump inhibitors (lansoprazole 30 mg or esomeprazole 20 mg), bismuth 220 or 200 mg, amoxicillin 1000 mg, and clarithromycin 500 mg, twice daily for 2 weeks by 1:1 propensity score matching analysis. The trial was registed on ClinicalTrials.gov (registration no. NCT05301725) | ||
520 | |a RESULTS: The H. pylori eradication rates of VPZ-based and PPI-based therapies were 88.8% (151/170) and 87.6% (149/170) in the intention-to-treat analysis, 94.1% (144/153) and 91.1% (144/158) in the per-protocol analysis, respectively. The noninferiority of VPZ to PPI was confirmed in all analyses (P < 0.001). The incidence of adverse events was 30.0% (51/170) and 27.1% (46/170) in the VPZ-based and PPI-based groups, respectively. VPZ-based and PPI-based therapies were well tolerated and showed good patient compliance without significant differences | ||
520 | |a CONCLUSIONS: VPZ-based therapy resulted in a satisfactory eradication rate and was well tolerated for H. pylori eradication, which are comparable to PPIs in C-BQT as a first-line treatment for H. pylori infection | ||
650 | 4 | |a Clinical Trial | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Helicobacter pylori | |
650 | 4 | |a bismuth-containing therapy | |
650 | 4 | |a propensity score matching | |
650 | 4 | |a proton pump inhibitors | |
650 | 4 | |a vonoprazan | |
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650 | 7 | |a Clarithromycin |2 NLM | |
650 | 7 | |a H1250JIK0A |2 NLM | |
650 | 7 | |a Proton Pump Inhibitors |2 NLM | |
700 | 1 | |a Li, Yue Yue |e verfasserin |4 aut | |
700 | 1 | |a Lin, Min Juan |e verfasserin |4 aut | |
700 | 1 | |a Liu, Jing |e verfasserin |4 aut | |
700 | 1 | |a Lin, Bo Shen |e verfasserin |4 aut | |
700 | 1 | |a Ding, Yu Ming |e verfasserin |4 aut | |
700 | 1 | |a Wan, Meng |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Wen Lin |e verfasserin |4 aut | |
700 | 1 | |a Kong, Qing Zhou |e verfasserin |4 aut | |
700 | 1 | |a Wang, Shao Tong |e verfasserin |4 aut | |
700 | 1 | |a Mu, Yi Jun |e verfasserin |4 aut | |
700 | 1 | |a Duan, Miao |e verfasserin |4 aut | |
700 | 1 | |a Han, Zhong Xue |e verfasserin |4 aut | |
700 | 1 | |a Zuo, Xiu Li |e verfasserin |4 aut | |
700 | 1 | |a Li, Yan Qing |e verfasserin |4 aut | |
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