Song Zhiqiang, Zuo Xiuli, Zhang Zhenyu, Wang Xuehong, Lin Ya, Li Yueyue, Xu Xiaojun, Huang Yun, Wang Qiuyan, Shi Yanyan, Zhou Liya
Department of Gastroenterology, Peking University Third Hospital, Beijing, China.
Department of Gastroenterology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Helicobacter. 2025 Sep-Oct;30(5):e70070. doi: 10.1111/hel.70070.
The optimal duration for vonoprazan and amoxicillin dual therapy (VA-DT) remains unclear, and studies on gastric acid suppression of vonoprazan during eradication are still lacking.
This study conducted a multicenter, randomized controlled trial to compare the eradication efficacy between 10 and 14-day VA-DT, and to identify the dynamic changes of gastric pH during treatment.
This study included 418 naïve adult patients with Helicobacter pylori infection, who were randomly divided into 10 or 14-day VA-DT groups (vonoprazan 20 mg twice daily and amoxicillin 1000 mg thrice daily). C-urea breath tests were conducted at 4-8 weeks after eradication to evaluate the success of treatment. 24-h intragastric pH was monitored in 22 patients.
Ten and 14-day VA-DT demonstrated eradication rates of 83.3% vs. 88.0% (rate difference: -4.8%, 95% confidence interval: -11.6% to -2.0%) in intention-to-treat analysis, 87.9% vs. 93.9% (-6.0%, -11.9% to -0.3%) in modified intention-to-treat analysis, and 89.1% vs. 95.3% (-6.1%, -11.8% to -0.7%) in per-protocol analysis, respectively. Vonoprazan showed excellent gastric acid suppression during eradication, with the time percentages of pH > 6 at 75.3% and 97.2% and the median pH levels at 7.4 and 7.8 on the 1st and 7th days, respectively. Furthermore, gastric pH exceeded 6 approximately 4-5 h after the first dose and remained stable at 7-9 thereafter.
The noninferiority of eradication efficacy between 10- and 14-day VA-DT in the first-line treatment was not established, indicating that 10-day therapy cannot be used as a substitute for 14-day therapy. Vonoprazan exerted excellent gastric acid suppression during eradication.
Chinese Clinical Trial Registry: ChiCTR2200057625.
沃克沙唑与阿莫西林联合治疗(VA-DT)的最佳疗程仍不明确,且关于根除治疗期间沃克沙唑抑制胃酸的研究仍很缺乏。
本研究进行了一项多中心随机对照试验,比较10天和14天VA-DT的根除疗效,并确定治疗期间胃内pH值的动态变化。
本研究纳入418例初治成年幽门螺杆菌感染患者,随机分为10天或14天VA-DT组(沃克沙唑20mg,每日2次;阿莫西林1000mg,每日3次)。根除治疗后4-8周进行C-尿素呼气试验以评估治疗效果。对22例患者进行24小时胃内pH值监测。
意向性分析中,10天和14天VA-DT的根除率分别为83.3%和88.0%(率差:-4.8%,95%置信区间:-11.6%至-2.0%);改良意向性分析中分别为87.9%和93.9%(-6.0%,-11.9%至-0.3%);符合方案分析中分别为89.1%和95.3%(-6.1%,-11.8%至-0.7%)。沃克沙唑在根除治疗期间显示出优异的胃酸抑制效果,第1天和第7天pH>6的时间百分比分别为75.3%和97.2%,中位pH值分别为7.4和7.8。此外,首次给药后约4-5小时胃内pH值超过6,此后稳定在7-9。
一线治疗中10天和14天VA-DT的根除疗效非劣效性未得到证实,表明10天治疗不能替代14天治疗。沃克沙唑在根除治疗期间发挥了优异的胃酸抑制作用。
中国临床试验注册中心:ChiCTR2200057625。