Ladrón-de-Guevara L, Bornstein-Quevedo L, González-Huezo S, Castañeda-Romero B, Costa F G, di Silvio-López M
Servicio de Gastroenterología, Hospital Ángeles Clínica Londres, Ciudad de México, México.
Laboratorio de Inmunohistoquímica y Patología Molecular, InmunoQ, Ciudad de México, México.
Rev Gastroenterol Mex (Engl Ed). 2019 Jul-Sep;84(3):274-283. doi: 10.1016/j.rgmx.2018.04.005. Epub 2018 Jul 27.
Helicobacter pylori (H. pylori) infection remains the leading cause of several gastroduodenal diseases. Despite the fact that multiple antibiotic regimens have been used to change its associated morbidity and mortality, the prevalence of this bacterial infection continues to be disproportionately high worldwide, mainly due to antibiotic resistance. To assess the noninferiority efficacy and safety of 210-day triple regimens on H. pylori eradication, we evaluated clarithromycin 500mg, lansoprazole 30mg, and amoxicillin 1g, all bid (standard triple therapy or CLA, Group 1) vs. pantoprazole 80mg, levofloxacin 500mg and azithromycin 500mg, all od (PLA, Group 2). Both regimens were compared in treatment-naïve patients.
An open label phase IIIb randomized and noninferiority trial comparing CLA vs. PLA was carried out for a 10-day period, within the time frame of June 2012 and March 2014. Eradication was verified with C-urea breath testing. Gastric biopsies were tested for fluorescence in situ hybridization (FISH)-clarithromycin resistance prior to any antibiotic administration. Efficacy and safety results were analyzed according to the noninferiority methodological approach.
From the 227 H. pylori positive subjects that were randomized, 194 were finally analyzed as per-protocol. The group 2 eradication rate was 63% and was noninferior to the group 1 eradication rate of 58.5% (upper limit 95% CI: 0.11608; below the noninferiority margin: 0.1200). FISH clarithromycin-resistance was found in 28.2% of the cases. Adverse events, all minor and self-limited, were significantly higher in group 1 than in group 2 (86 vs. 65.4%; p=0.001).
First-line H. pylori eradication with pantoprazole/levofloxacin/azithromycin combination therapy is as effective as the standard triple therapy, with better tolerability and easier dosing. Clarithromycin resistance should be considered when selecting antibiotics in Helicobacter pylori eradication treatments. ClinicalTrials.gov identifier NCT02726269.
幽门螺杆菌(H. pylori)感染仍然是多种胃十二指肠疾病的主要病因。尽管已使用多种抗生素方案来改变其相关的发病率和死亡率,但这种细菌感染在全球的患病率仍然高得不成比例,主要原因是抗生素耐药性。为评估210天三联疗法根除幽门螺杆菌的非劣效性疗效和安全性,我们比较了克拉霉素500mg、兰索拉唑30mg和阿莫西林1g,均每日两次(标准三联疗法或CLA,第1组)与泮托拉唑80mg、左氧氟沙星500mg和阿奇霉素500mg,均每日一次(PLA,第2组)。两种方案均在初治患者中进行比较。
在2012年6月至2014年3月期间,进行了一项为期10天的开放标签IIIb期随机非劣效性试验,比较CLA与PLA。通过C-尿素呼气试验验证根除情况。在给予任何抗生素之前,对胃活检组织进行荧光原位杂交(FISH)检测克拉霉素耐药性。根据非劣效性方法分析疗效和安全性结果。
在随机分组的227例幽门螺杆菌阳性受试者中,最终按方案分析了194例。第2组的根除率为63%,不劣于第1组的根除率58.5%(95%CI上限:0.11608;低于非劣效性界值:0.1200)。28.2%的病例检测到FISH克拉霉素耐药。不良事件均为轻微且自限性,第1组显著高于第2组(86%对65.4%;p = 0.001)。
泮托拉唑/左氧氟沙星/阿奇霉素联合疗法一线根除幽门螺杆菌与标准三联疗法同样有效,耐受性更好且给药更方便。在幽门螺杆菌根除治疗中选择抗生素时应考虑克拉霉素耐药性。ClinicalTrials.gov标识符:NCT02726269。