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Efficacy of first-line levofloxacin-based therapy for Helicobacter pylori eradication. Results from a single tertiary center cohort in Argentina

Pedro Elía, María Florencia Álvarez, Sandy Mark Trenholm, Matías Martínez, Roberto Chamale, D. Balderramo

Gastroenterology & hepatology, 2026

277 participants

Abstract

BACKGROUND AND OBJECTIVE

Helicobacter pylori (H. pylori) colonizes the gastric mucosa in approximately half of the global population and is a well-established risk factor for peptic ulcer disease and gastric adenocarcinoma. Data on the effectiveness of levofloxacin-based eradication regimens in Argentina remain scarce. The objective of the study was to evaluate the eradication efficacy of a 14-day levofloxacin-containing triple therapy regimen in treatment-naïve patients with H. pylori infection.

PATIENTS AND METHODS

This single-center retrospective study included treatment-naïve adult patients with histologically confirmed H. pylori infection between 09/2020-07/2023. Patients received a 14-day regimen consisting of amoxicillin 1 g twice daily, levofloxacin 500 mg once daily, and pantoprazole 40 mg twice daily. Eradication was assessed by ¹³C-urea breath test performed at least 4 weeks following treatment completion.

RESULTS

The study included 277 patients (median age 57 years; 60.6% female). The eradication rate was 76.2% evaluated through modified intention to treat analysis. Eradication rates did not differ by age, sex, body mass index, or other baseline clinical characteristics. Treatment-related adverse events occurred in 11 (4%) patients and 6 (2.2%) patients did not complete the prescribed treatment regimen due to adverse events.

CONCLUSION

The 14-day levofloxacin-based triple therapy regimen achieved a suboptimal H. pylori eradication rate, falling below the…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 277 participants or records.

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