Evidence map›Paper›PMID 39090833›Full record

Observational studyUnited European gastroenterology journal2024

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.

Patricio Medel-Jara, Diego Reyes Placencia, Eduardo Fuentes-López, Oscar Corsi, Gonzalo Latorre, Rosario Antón, Elena Jiménez, Ana Miralles-Marco, Carmelo Caballero, Hugo Boggino and 22 more

Abstract readMulticenter StudyObservational StudyComparative Study
In one paragraph

Observational study in United European gastroenterology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Adjunctive Synbiotic Therapy forLife (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Overcoming antibiotic-resistantWorld journal of gastroenterology · 2025
    Review
  6. Therapeutic advances and future directions inFrontiers in microbiology · 2025
    Review
  7. Observational
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors.

Patricio Medel-JaraFacultad de Medicina, Programa de Doctorado en Epidemiología, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0003-3784-1463
Diego Reyes PlacenciaDepartamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0001-6371-3516
Eduardo Fuentes-LópezFacultad de Medicina, Departamento de Ciencias de la Salud, Pontificia Universidad Católica de Chile, Santiago, Chile.
Oscar CorsiDepartamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Gonzalo LatorreDepartamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Rosario AntónDigestive Medicine Department, Hospital Clínico Universitario de Valencia, Valencia, Spain.
Elena JiménezINCLIVA Biomedical Research Institute, Valencia, Spain.
Ana Miralles-MarcoINCLIVA Biomedical Research Institute, Valencia, Spain.
Carmelo CaballeroGenPat Laboratory, Asunción, Paraguay.
Hugo BogginoGenPat Laboratory, Asunción, Paraguay.
Daniel CanteroEndoscopy Department, Instituto de Previsión Social, Asunción, Paraguay.
Rita BarrosIPATIMUP - Institute of Pathology and Molecular Immunology of the University of Porto, Porto, Portugal.
João Santos-AntunesIPATIMUP - Institute of Pathology and Molecular Immunology of the University of Porto, Porto, Portugal.ORCID 0000-0003-0614-0576
Marc DíezVall d'Hebron University, Barcelona, Spain.
Luis A QuiñonesFaculty of Medicine, Department of Basic and Clinical Oncology, Laboratory of Chemical Carcinogenesis and Pharmacogenetics (CQF), University of Chile, Santiago, Chile.
Erick RiquelmeDepartamento de Enfermedades Respiratorias, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Antonio RollánFacultad de Medicina Clínica Alemana-Universidad del Desarrollo, Unidad de Gastroenterología, Santiago, Chile.
Leslie C CerpaFaculty of Medicine, Department of Basic and Clinical Oncology, Laboratory of Chemical Carcinogenesis and Pharmacogenetics (CQF), University of Chile, Santiago, Chile.
Ivania ValdésDoctorate Program, Integrative Genomics, Universidad Mayor, Santiago, Chile.
Olga P NyssenServicio de Aparato Digestivo. Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), Madrid, Spain.ORCID 0000-0002-4920-9310
Leticia MoreiraHospital 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.
Javier P GisbertServicio de Aparato Digestivo. Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), Madrid, Spain.
M Constanza CamargoDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
Nayeli Ortiz-OlveraDepartamento de Gastroenterología, UMAE, Hospital de Especialidades "Dr. Bernardo Sepúlveda", Centro Médico Nacional Siglo XXI, IMSS, Ciudad de México, México.
Alberto M Leon-TakahashiDepartamento de Gastroenterología, Instituto Nacional de Cancerología, Ciudad de México, México.ORCID 0000-0001-8031-8358
Erika Ruiz-GarciaDepartamento de Gastroenterología, Instituto Nacional de Cancerología, Ciudad de México, México.ORCID 0000-0002-0446-123X
Edith A Fernández-FigueroaNúcleo B de Innovación en Medicina de Precisión. Instituto Nacional de Medicina Genómica, Ciudad de México, México.
Marcelo GarridoCentro de Oncología de Precisión, Escuela de Medicina, Universidad Mayor, Santiago, Chile.
Gareth I OwenCentro para la Prevención y el Control del Cáncer (CECAN), Santiago, Chile.
Andrés CervantesINCLIVA Biomedical Research Institute, Valencia, Spain.
Tania FleitasINCLIVA Biomedical Research Institute, Valencia, Spain.ORCID 0000-0002-2789-9082
Arnoldo RiquelmeDepartamento de Gastroenterología, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.ORCID 0000-0002-8259-8960

Funding

CECAN: Centro para la prevención y el control del cáncer 152220002CONACyT Unión Europea-CELAC 297681FONDECYT Role of the genomic and microbiome profile in gastric carcinogenesis: prospective endoscopic follow-up 1230504Fondo de Financiamiento de Centros de Investigación en Áreas Prioritarias 15130011Fondo Nacional de Desarrollo científico y Tecnológico 11201338Fondo Nacional de Desarrollo científico y Tecnológico 1211948Fondo Nacional de Desarrollo científico y Tecnológico 1220586FONIS SA19/0188HORIZON EUROPE Innovative Europe 825832Program ICN-ANID ICN2021_045
6 · The paper itself

Abstract

introductionGastric 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.

Indexed as

Anti-Bacterial AgentsDrug Therapy, CombinationHelicobacter InfectionsHelicobacter pyloriProton Pump InhibitorsAdultAgedAmoxicillinBismuthClarithromycinCytochrome P-450 CYP2C19Drug Resistance, BacterialEuropeFemaleHumansLatin AmericaAmoxicillinAnti-Bacterial AgentsBismuthClarithromycinCYP2C19 protein, humanCytochrome P-450 CYP2C19MetronidazoleProton Pump Inhibitorscombination drug therapiesgastric cancerHelicobacter pyloriquadruple therapystandard triple therapy

Identifiers

PMID39090833
PMCPMC11578845

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.