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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.
Medel-Jara, Patricio; Reyes Placencia, Diego; Fuentes-López, Eduardo; Corsi, Oscar; Latorre, Gonzalo; Antón, Rosario; Jiménez, Elena; Miralles-Marco, Ana; Caballero, Carmelo; Boggino, Hugo; Cantero, Daniel; Barros, Rita; Santos-Antunes, João; Díez, Marc; Quiñones, Luis A; Riquelme, Erick; Rollán, Antonio; Cerpa, Leslie C; Valdés, Ivania; Nyssen, Olga P; Moreira, Leticia; Gisbert, Javier P; Camargo, M Constanza; Ortiz-Olvera, Nayeli; Leon-Takahashi, Alberto M; Ruiz-Garcia, Erika; Fernández-Figueroa, Edith A; Garrido, Marcelo; Owen, Gareth I; Cervantes, Andrés; Fleitas, Tania; Riquelme, Arnoldo.
Affiliation
  • Medel-Jara P; Facultad de Medicina, Programa de Doctorado en Epidemiología, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Reyes Placencia D; Facultad de Medicina, Programa de Farmacología y Toxicología, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Fuentes-López E; Facultad de Medicina, Carrera de Terapia Ocupacional, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Corsi O; Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Latorre G; Facultad de Medicina, Departamento de Ciencias de la Salud, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Antón R; Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Jiménez E; Departamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Miralles-Marco A; Digestive Medicine Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
  • Caballero C; Biochemistry Department and Molecular Biology, Universidad de Valencia, Valencia, Spain.
  • Boggino H; INCLIVA Biomedical Research Institute, Valencia, Spain.
  • Cantero D; INCLIVA Biomedical Research Institute, Valencia, Spain.
  • Barros R; GenPat Laboratory, Asunción, Paraguay.
  • Santos-Antunes J; GenPat Laboratory, Asunción, Paraguay.
  • Díez M; Endoscopy Department, Instituto de Previsión Social, Asunción, Paraguay.
  • Quiñones LA; IPATIMUP - Institute of Pathology and Molecular Immunology of the University of Porto, Porto, Portugal.
  • Riquelme E; Department of Pathology, Medical Faculty of the University of Porto, Porto, Portugal.
  • Rollán A; IPATIMUP - Institute of Pathology and Molecular Immunology of the University of Porto, Porto, Portugal.
  • Cerpa LC; Department of Gastroenterology, Centro Hospitalar Universitário de S. João, Porto, Portugal.
  • Valdés I; Department of Gastroenterology, Medical Faculty of the University of Porto, Porto, Portugal.
  • Nyssen OP; Vall d'Hebron University, Barcelona, Spain.
  • Moreira L; Hospital-Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • Gisbert JP; Faculty of Medicine, Department of Basic and Clinical Oncology, Laboratory of Chemical Carcinogenesis and Pharmacogenetics (CQF), University of Chile, Santiago, Chile.
  • Camargo MC; Faculty of Chemical and Pharmaceutical Sciences, Department of Pharmaceutical Sciences and Technology, University of Chile, Santiago, Chile.
  • Ortiz-Olvera N; Latin American Network for Implementation and Validation of Clinical Pharmacogenomics Guidelines (RELIVAF), Santiago, Chile.
  • Leon-Takahashi AM; Departamento de Enfermedades Respiratorias, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Ruiz-Garcia E; Centro para la Prevención y el Control del Cáncer (CECAN), Santiago, Chile.
  • Fernández-Figueroa EA; Facultad de Medicina Clínica Alemana-Universidad del Desarrollo, Unidad de Gastroenterología, Santiago, Chile.
  • Garrido M; Faculty of Medicine, Department of Basic and Clinical Oncology, Laboratory of Chemical Carcinogenesis and Pharmacogenetics (CQF), University of Chile, Santiago, Chile.
  • Owen GI; Latin American Network for Implementation and Validation of Clinical Pharmacogenomics Guidelines (RELIVAF), Santiago, Chile.
  • Cervantes A; Doctorate Program, Integrative Genomics, Universidad Mayor, Santiago, Chile.
  • Fleitas T; Servicio de Aparato Digestivo. Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), Madrid, Spain.
  • Riquelme A; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
Article in En | MEDLINE | ID: mdl-39090833
ABSTRACT

INTRODUCTION:

Gastric 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.

OBJECTIVE:

To 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.

METHODS:

A 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.

RESULTS:

772 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.

CONCLUSIONS:

Both 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: United European Gastroenterol J Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: United European Gastroenterol J Year: 2024 Document type: Article Affiliation country: Country of publication: