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基于新型钾离子竞争性酸阻滞剂替戈拉赞的三联疗法用于一线治疗感染:一项随机、双盲、III 期临床试验。

Triple Therapy-Based on Tegoprazan, a New Potassium-Competitive Acid Blocker, for First-Line Treatment of Infection: A Randomized, Double-Blind, Phase III, Clinical Trial.

机构信息

Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.

Department of Microbiology and Institute of Biomedical Science, Hanyang University College of Medicine, Seoul, Korea.

出版信息

Gut Liver. 2022 Jul 15;16(4):535-546. doi: 10.5009/gnl220055. Epub 2022 Jul 6.

DOI:10.5009/gnl220055
PMID:
35791797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9289827/
Abstract

BACKGROUND/AIMS: We examined the efficacy and safety of tegoprazan as a part of first-line triple therapy for eradication.

METHODS

A randomized, double-blind, controlled, multicenter study was performed to evaluate whether tegoprazan (50 mg)-based triple therapy (TPZ) was noninferior to lansoprazole (30 mg)- based triple therapy (LPZ) (with amoxicillin 1 g and clarithromycin 500 mg; all administered twice daily for 7 days) for treating . The primary endpoint was the eradication rate. Subgroup analyses were performed according to the cytochrome P450 (CYP) 2C19 genotype, the minimum inhibitory concentration (MIC) of amoxicillin and clarithromycin, and underlying gastric diseases.

RESULTS

In total, 350 -positive patients were randomly allocated to the TPZ or LPZ group. The eradication rates in the TPZ and LPZ groups were 62.86% (110/175) and 60.57% (106/175) in an intention-to-treat analysis and 69.33% (104/150) and 67.33% (101/150) in a per-protocol analysis (non-inferiority test, p=0.009 and p=0.013), respectively. Subgroup analyses according to MICs or CYP2C19 did not show remarkable differences in eradication rate. Both first-line triple therapies were well-tolerated with no notable differences.

CONCLUSIONS

TPZ is as effective as proton pump inhibitor-based triple therapy and is as safe as first-line eradication therapy but does not overcome the clarithromycin resistance of in Korea (ClinicalTrials.gov identifier NCT03317223).

摘要

背景/目的:我们研究了替波拉唑作为一线三联疗法根除治疗的疗效和安全性。

方法

一项随机、双盲、对照、多中心研究评估了替波拉唑(50mg)为基础的三联疗法(TPZ)是否不劣于兰索拉唑(30mg)为基础的三联疗法(LPZ)(联合阿莫西林 1g 和克拉霉素 500mg;均每日 2 次,疗程 7 天)治疗幽门螺杆菌感染。主要终点是根除率。根据细胞色素 P450(CYP)2C19 基因型、阿莫西林和克拉霉素的最低抑菌浓度(MIC)以及潜在的胃部疾病进行亚组分析。

结果

共纳入 350 例幽门螺杆菌阳性患者随机分配至 TPZ 或 LPZ 组。意向治疗分析中,TPZ 组和 LPZ 组的根除率分别为 62.86%(110/175)和 60.57%(106/175),按方案分析分别为 69.33%(104/150)和 67.33%(101/150)(非劣效性检验,p=0.009 和 p=0.013)。根据 MIC 或 CYP2C19 的亚组分析,根除率无显著差异。两种一线三联疗法均具有良好的耐受性,无显著差异。

结论

TPZ 与质子泵抑制剂为基础的三联疗法疗效相当,与一线幽门螺杆菌根除治疗安全性相当,但未能克服韩国幽门螺杆菌对克拉霉素的耐药性(ClinicalTrials.gov 标识符 NCT03317223)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/4908ec1cfc9e/gnl-16-4-535-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/b4ff16b4c504/gnl-16-4-535-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/9ed19c9311a0/gnl-16-4-535-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/c14bdfba96d5/gnl-16-4-535-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/0ae94d323f5d/gnl-16-4-535-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/4908ec1cfc9e/gnl-16-4-535-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/b4ff16b4c504/gnl-16-4-535-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/9ed19c9311a0/gnl-16-4-535-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/c14bdfba96d5/gnl-16-4-535-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/0ae94d323f5d/gnl-16-4-535-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8447/9289827/4908ec1cfc9e/gnl-16-4-535-f5.jpg

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