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沃克-阿莫西林双重疗法用于中国人群根除幽门螺杆菌:一项前瞻性、多中心、随机、两阶段研究。

Vonoprazan-amoxicillin dual therapy for eradication in Chinese population: A prospective, multicenter, randomized, two-stage study.

作者信息

Huang Xue-Ping, Liu Yi-Juan, Lin Shao-Wei, Shao Yan-Feng, Qiu Feng, Qiu Qing-Wu, Xu Zhang-Kun, Chen Jin-Xian, Chen Liang-Huo, Lin Zhen-Qun, Dai Wen-Hua, Zhang Ming-Qing, Jiang Qi, Xiao Zhong-Qin, Cheng Xian-Xing, Zhang Xiang-Fei, You Wen-Bin, Chen Wei, Li Long-Qin, Lin Wei-Xing, Wang Yong-Fu, Lai Fu-Jin, Chen Long-Qun, Huang Zhong-Hua, Zheng Wen-Qi, Wei Jin-Qi, Lin Zhi-Hui

机构信息

Department of Gastroenterology, Shengli Clinical Medical College of Fujian Medical University, Fuzhou 350000, Fujian Province, China.

Department of Gastroenterology, Fujian Provincial Hospital, Fuzhou 350001, Fujian Province, China.

出版信息

World J Gastroenterol. 2024 Jul 21;30(27):3304-3313. doi: 10.3748/wjg.v30.i27.3304.

Abstract

BACKGROUND

The efficacy of Vonoprazan-amoxicillin dual therapy (VAT) in the treatment of () is controversial.

AIM

To evaluate the efficacy of VAT in the Chinese population.

METHODS

This prospective, multicenter, randomized, open-label, and two-stage study was conducted at 23 centers in Fujian, China (May 2021-April 2022). -infected patients were randomized to bismuth quadruple therapy (BQT), BQT-Vonoprazan (BQT-V), seven-day VAT (VAT-7), ten-day VAT (VAT-10), and fourteen-day VAT (VAT-14) groups. The primary endpoint was the eradication rate. The secondary endpoint was the frequency of adverse events. This study was registered with the Chinese Clinical Trial Registry, ChiCTR2100045778.

RESULTS

In the first stage, VAT-7 and BQT-V groups were selected for early termination because less than 23 among 28 cases were eradicated. In the second stage, the eradication rates for BQT, VAT-10, and VA-14 were 80.2% [95% confidence interval (95%CI): 71.4%-86.8%], 93.2% (86.6%-96.7%), 92.2% (85.3%-96.0%) in the intention-to-treat (ITT) analysis, and 80.9% (95%CI: 71.7%-87.5%), 94.0% (87.5%-97.2%), and 93.9% (87.4%-97.2%) in the per-protocol analysis. The ITT analysis showed a higher eradication rate in the VAT-10 and VAT-14 groups than in the BQT group ( = 0.022 and = 0.046, respectively). The incidence of adverse events in the VAT-10 and VAT-14 groups was lower than in the BQT group (25.27% and 13.73% 37.62%, respectively; < 0.001).

CONCLUSION

VAT with a duration of 10 or 14 days achieves a higher eradication rate than the BQT, with a more tolerable safety profile in -infected patients in Fujian.

摘要

背景

沃克帕唑-阿莫西林联合疗法(VAT)治疗()的疗效存在争议。

目的

评估VAT在中国人群中的疗效。

方法

本前瞻性、多中心、随机、开放标签的两阶段研究在中国福建的23个中心进行(2021年5月至2022年4月)。将()感染患者随机分为铋剂四联疗法(BQT)组、BQT-沃克帕唑(BQT-V)组、7天VAT(VAT-7)组、10天VAT(VAT-10)组和14天VAT(VAT-14)组。主要终点是()根除率。次要终点是不良事件的发生频率。本研究已在中国临床试验注册中心注册,注册号为ChiCTR2100045778。

结果

在第一阶段,VAT-7组和BQT-V组因28例中根除例数少于23例而被提前终止。在第二阶段,意向性分析(ITT)中,BQT组、VAT-10组和VAT-14组的根除率分别为80.2%[95%置信区间(95%CI):71.4%-86.8%]、93.2%(86.6%-96.7%)、92.2%(85.3%-96.0%),符合方案分析中分别为80.9%(95%CI:71.7%-87.5%)、94.0%(87.5%-97.2%)、93.9%(87.4%-97.2%)。ITT分析显示,VAT-10组和VAT-14组的根除率高于BQT组(分别为 = 0.022和 = 0.046)。VAT-10组和VAT-14组不良事件的发生率低于BQT组(分别为25.27%和13.73%对37.62%; < 0.001)。

结论

为期10天或14天的VAT比BQT实现了更高的根除率,在福建()感染患者中安全性更易耐受。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ddf/11287422/93d30069e9f4/WJG-30-3304-g001.jpg

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