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利福布汀、甲硝唑和沃克拉唑根除挽救治疗的单臂前瞻性干预研究

Single-Arm, Prospective, Interventional Study of Eradication Rescue Therapy with Rifabutin, Metronidazole, and Vonoprazan.

作者信息

Sue Soichiro, Ikeda Ryosuke, Ikeda Aya, Sato Hiroki, Kaneko Hiroaki, Irie Kuniyasu, Maeda Shin

机构信息

Department of Gastroenterology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.

出版信息

J Clin Med. 2024 Jun 27;13(13):3774. doi: 10.3390/jcm13133774.

Abstract

Rescue eradication can be challenging. Rifabutin (RBT) demonstrates high activity against and is incorporated into various rescue eradication regimens. This exploratory study was performed to evaluate the efficacy and safety of a rescue regimen comprising RBT, metronidazole (MNZ), and vonoprazan (VPZ). This prospective, single-center, single-arm, interventional study was performed in Japan. Eligible patients were those who underwent failed primary eradication treatment (7-day treatment with three drugs: VPZ or a proton pump inhibitor [PPI], amoxicillin [AMPC], and clarithromycin) and secondary eradication treatment (7-day treatment with three drugs: VPZ or a PPI, AMPC, and MNZ) and those who were unable to receive first- and second-line therapy because of penicillin allergy. Twenty -positive patients were treated with RBT (150 mg twice daily), MNZ (250 mg twice daily), and VPZ (20 mg twice daily) for 10 days (RBT-MNZ-VPZ therapy). Eradication success was evaluated using the urea breath test. Drug susceptibility test results were available in 16 patients. This study is registered in the Japan Registry of Clinical Trials (jRCT031220504). The intention-to-treat (ITT) and per-protocol (PP) eradication rates of RBT-MNZ-VPZ therapy were 70% (90% confidence interval [CI]: 49.2%-86.0%) and 72.2% (95% CI: 50.2%-88.4%), respectively. In the MNZ-susceptible subgroup, the ITT ( = 8) and PP ( = 7) eradication rates were 100% (90% CI: 68.8%-100%) and 100% (90% CI: 65.2%-100%). In the MNZ-resistant subgroup, the ITT ( = 8) and PP ( = 7) eradication rates were both 62.5% (90% CI: 28.9%-88.9%). All infections were RBT-susceptible. These findings suggest that RBT-MNZ-VPZ therapy may be a promising rescue regimen, especially in MNZ- and RBT-susceptible infections or patients with penicillin allergy.

摘要

挽救性根除治疗可能具有挑战性。利福布汀(RBT)对幽门螺杆菌显示出高活性,并被纳入各种挽救性根除方案。本探索性研究旨在评估由RBT、甲硝唑(MNZ)和沃克(VPZ)组成的挽救方案的疗效和安全性。 这项前瞻性、单中心、单臂干预性研究在日本进行。符合条件的患者为初次根除治疗失败(使用三种药物进行7天治疗:VPZ或质子泵抑制剂[PPI]、阿莫西林[AMPC]和克拉霉素)和二次根除治疗失败(使用三种药物进行7天治疗:VPZ或PPI、AMPC和MNZ)的患者,以及因青霉素过敏而无法接受一线和二线治疗的患者。20例幽门螺杆菌阳性患者接受RBT(每日2次,每次150 mg)、MNZ(每日2次,每次250 mg)和VPZ(每日2次,每次20 mg)治疗10天(RBT-MNZ-VPZ疗法)。使用尿素呼气试验评估根除成功率。16例患者可获得药敏试验结果。本研究已在日本临床试验注册中心(jRCT031220504)注册。RBT-MNZ-VPZ疗法的意向性治疗(ITT)和符合方案(PP)根除率分别为70%(90%置信区间[CI]:49.2%-86.0%)和72.2%(95%CI:50.2%-88.4%)。在MNZ敏感亚组中,ITT(n = 8)和PP(n = 7)根除率均为100%(90%CI:68.8%-100%)和100%(90%CI:65.2%-100%)。在MNZ耐药亚组中,ITT(n = 8)和PP(n = 7)根除率均为62.5%(90%CI:28.9%-88.9%)。所有感染均对RBT敏感。 这些研究结果表明,RBT-MNZ-VPZ疗法可能是一种有前景的挽救方案,尤其是在对MNZ和RBT敏感的感染或青霉素过敏的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a4a/11242301/5e6db636b50b/jcm-13-03774-g001.jpg

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