Lin Aiping, Lin Zhihui, Liu Yijuan, Chen Shuo, Shao Yanfeng, Qiu Feng, Xiao Zhongqin, Xu Zhangkun, Chen Longqun, Chen Lianghuo, Lin Weixing, Wang Yongfu, Huang Zhonghua, Lin Zhenqun, Huang Xueping
Department of Gastroenterology, Shengli Clinical Medical College of Fujian Medical University, Fuzhou, China.
Department of Gastroenterology, Fujian Provincial Hospital, Fuzhou, China.
J Gastroenterol Hepatol. 2024 Dec;39(12):2645-2653. doi: 10.1111/jgh.16761. Epub 2024 Nov 24.
Only a few studies have investigated the efficacy and safety of different durations of vonoprazan and amoxicillin (VA) high-dose dual therapy for the eradication of Helicobacter pylori. We aimed to compare the efficacy and safety of 10 days versus 14 days of VA high-dose dual therapy for H. pylori eradication.
This study was conducted in 14 centers in China. A total of 250 patients infected with H. pylori were randomly assigned to Group VA-10 or VA-14. Both groups received the VA dual therapy (vonoprazan 20 mg twice daily + amoxicillin 1000 mg three times daily). The primary endpoint was the H. pylori eradication rate. Secondary endpoints included adverse events and patient compliance.
Group VA-10 achieved eradication rates of 89.60%, 91.06%, and 91.67% as determined by the intention-to-treat (ITT), modified intention-to-treat (MITT), and per-protocol (PP) analysis, respectively. The eradication rates were similar to those in Group VA-14: 91.20%, 93.44%, and 93.39%. The difference and 90% confidence interval boundary -1.60% (-7.73% to 4.53%) in the ITT analysis, -2.39% (-8.00% to 3.23%) in the MITT analysis, and -1.72% (-7.29% to 3.85%) in the PP analysis were greater than the predefined noninferiority margin of -10%, establishing a noninferiority of Group VA-10 versus Group VA-14 (noninferiority P = 0.001 in ITT analysis, P < 0.001 in MITT analysis, and P < 0.001 in PP analysis, respectively). No significant differences were observed in adverse events between the two groups.
Ten-day VA dual therapy achieves comparable efficacy and safety to the 14-day regimen in Chinese population, providing patients with greater convenience and economic benefits.
仅有少数研究调查了不同疗程的沃克帕唑与阿莫西林(VA)高剂量双联疗法根除幽门螺杆菌的疗效和安全性。我们旨在比较10天与14天的VA高剂量双联疗法根除幽门螺杆菌的疗效和安全性。
本研究在中国的14个中心进行。共有250例幽门螺杆菌感染患者被随机分配至VA-10组或VA-14组。两组均接受VA双联疗法(沃克帕唑20 mg,每日2次 + 阿莫西林1000 mg,每日3次)。主要终点是幽门螺杆菌根除率。次要终点包括不良事件和患者依从性。
VA-10组在意向性分析(ITT)、改良意向性分析(mITT)和符合方案分析(PP)中确定的根除率分别为89.60%、91.06%和91.67%。根除率与VA-14组相似:分别为91.20%、93.44%和93.39%。ITT分析中的差异和90%置信区间边界为-1.60%(-7.73%至4.53%),mITT分析中为-2.39%(-8.00%至3.23%),PP分析中为-1.72%(-7.29%至3.85%),均大于预先设定的非劣效性界值-10%,确立了VA-10组相对于VA-14组的非劣效性(ITT分析中非劣效性P = 0.001,mITT分析中P < 0.001,PP分析中P < 0.001)。两组之间不良事件无显著差异。
在中国人群中,10天的VA双联疗法与14天疗程的疗效和安全性相当,为患者提供了更大的便利性和经济效益。