Quadruple therapies show a higher eradication rate compared to standard triple therapy for Helicobacter pylori infection within the LEGACy consortium. A multicenter observational study in European and Latin American countries

Author:

Medel‐Jara Patricio123ORCID,Reyes Placencia Diego4ORCID,Fuentes‐López Eduardo5,Corsi Oscar4,Latorre Gonzalo4,Antón Rosario67,Jiménez Elena8,Miralles‐Marco Ana8,Caballero Carmelo9,Boggino Hugo9,Cantero Daniel10,Barros Rita1112,Santos‐Antunes João111314ORCID,Díez Marc1516,Quiñones Luis A.171819,Riquelme Erick2021,Rollán Antonio22,Cerpa Leslie C.1719,Valdés Ivania23,Nyssen Olga P.2425ORCID,Moreira Leticia26,Gisbert Javier P.2425,Camargo M. Constanza27,Ortiz‐Olvera Nayeli28,Leon‐Takahashi Alberto M.29ORCID,Ruiz‐Garcia Erika2930ORCID,Fernández‐Figueroa Edith A.31,Garrido Marcelo32,Owen Gareth I.21333435,Cervantes Andrés836,Fleitas Tania836ORCID,Riquelme Arnoldo421ORCID

Affiliation:

1. Facultad de Medicina Programa de Doctorado en Epidemiología Pontificia Universidad Católica de Chile Santiago Chile

2. Facultad de Medicina Programa de Farmacología y Toxicología Pontificia Universidad Católica de Chile Santiago Chile

3. Facultad de Medicina Carrera de Terapia Ocupacional Pontificia Universidad Católica de Chile Santiago Chile

4. Departamento de Gastroenterología Escuela de Medicina Pontificia Universidad Católica de Chile Santiago Chile

5. Facultad de Medicina Departamento de Ciencias de la Salud Pontificia Universidad Católica de Chile Santiago Chile

6. Digestive Medicine Department Hospital Clínico Universitario de Valencia Valencia Spain

7. Biochemistry Department and Molecular Biology Universidad de Valencia Valencia Spain

8. INCLIVA Biomedical Research Institute Valencia Spain

9. GenPat Laboratory Asunción Paraguay

10. Endoscopy Department Instituto de Previsión Social Asunción Paraguay

11. IPATIMUP ‐ Institute of Pathology and Molecular Immunology of the University of Porto Porto Portugal

12. Department of Pathology Medical Faculty of the University of Porto Porto Portugal

13. Department of Gastroenterology Centro Hospitalar Universitário de S. João Porto Portugal

14. Department of Gastroenterology Medical Faculty of the University of Porto Porto Portugal

15. Vall d'Hebron University Barcelona Spain

16. Hospital‐Vall d’Hebron Institute of Oncology (VHIO) Barcelona Spain

17. Faculty of Medicine Department of Basic and Clinical Oncology Laboratory of Chemical Carcinogenesis and Pharmacogenetics (CQF) University of Chile Santiago Chile

18. Faculty of Chemical and Pharmaceutical Sciences Department of Pharmaceutical Sciences and Technology University of Chile Santiago Chile

19. Latin American Network for Implementation and Validation of Clinical Pharmacogenomics Guidelines (RELIVAF) Santiago Chile

20. Departamento de Enfermedades Respiratorias Escuela de Medicina Pontificia Universidad Católica de Chile Santiago Chile

21. Centro para la Prevención y el Control del Cáncer (CECAN) Santiago Chile

22. Facultad de Medicina Clínica Alemana—Universidad del Desarrollo Unidad de Gastroenterología Santiago Chile

23. Doctorate Program Integrative Genomics Universidad Mayor Santiago Chile

24. Servicio de Aparato Digestivo. Hospital Universitario de La Princesa Instituto de Investigación Sanitaria Princesa (IIS‐Princesa) Universidad Autónoma de Madrid (UAM) Madrid Spain

25. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd) Madrid Spain

26. Hospital Clínic de Barcelona Centro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBERehd) IDIBAPS (Institut d’Investigacions Biomèdiques August Pi i Sunyer) University of Barcelona Barcelona Spain

27. Division of Cancer Epidemiology and Genetics National Cancer Institute Rockville Maryland USA

28. Departamento de Gastroenterología UMAE Hospital de Especialidades “Dr. Bernardo Sepúlveda” Centro Médico Nacional Siglo XXI IMSS Ciudad de México México

29. Departamento de Gastroenterología Instituto Nacional de Cancerología Ciudad de México México

30. Laboratorio de Medicina Traslacional Instituto Nacional de Cancerología Ciudad de México México

31. Núcleo B de Innovación en Medicina de Precisión. Instituto Nacional de Medicina Genómica Ciudad de México México

32. Centro de Oncología de Precisión Escuela de Medicina Universidad Mayor Santiago Chile

33. Faculty of Biological Sciences Faculty of Medicine Pontificia Universidad Católica de Chile Santiago Chile

34. Millennium Institute on Immunology and Immunotherapy Santiago Chile

35. Advanced Center for Chronic Diseases Santiago Chile

36. Medical Oncology Department Hospital Clínico Universitario de Valencia Valencia Spain

Abstract

AbstractIntroductionGastric cancer (GC) is one of the most lethal malignancies worldwide. Helicobacter pylori is the primary cause of GC; therefore, its eradication reduces the risk of developing this neoplasia. There is extensive evidence regarding quadruple therapy with relevance to the European population. However, in Latin America, data are scarce. Furthermore, there is limited information about the eradication rates achieved by antibiotic schemes in European and Latin American populations.ObjectiveTo compare the effectiveness of standard triple therapy (STT), quadruple concomitant therapy (QCT), and bismuth quadruple therapy (QBT) in six centers in Europe and Latin America.MethodsA retrospective study was carried out based on the LEGACy registry from 2017 to 2022. Data from adult patients recruited in Portugal, Spain, Chile, Mexico, and Paraguay with confirmed H. pylori infection who received eradication therapy and confirmatory tests at least 1 month apart were included. Treatment success by each scheme was compared using a mixed multilevel Poisson regression, adjusting for patient sex and age, together with country‐specific variables, including prevalence of H. pylori antibiotic resistance (clarithromycin, metronidazole, and amoxicillin), and CYP2C19 polymorphisms.Results772 patients were incorporated (64.64% females; mean age of 52.93 years). The total H. pylori eradication rates were 75.20% (255/339) with STT, 88.70% (159/178) with QCT, and 91.30% (191/209) with QBT. Both quadruple therapies (QCT‐QBT) showed significantly higher eradication rates compared with STT, with an adjusted incidence risk ratio (IRR) of 1.25 (p: <0.05); and 1.24 (p: <0.05), respectively. The antibiotic‐resistance prevalence by country, but not the prevalence of CYP2C19 polymorphism, showed a statistically significant impact on eradication success.ConclusionsBoth QCT and QBT are superior to STT for H. pylori eradication when adjusted for country‐specific antibiotic resistance and CYP2C19 polymorphism in a sample of individuals residing in five countries within two continents.

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Wiley

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