Evidence map›Paper›PMID 40576027›Full record

ArticleCancer medicine2025

Validation of the ABC Method for Gastric Cancer Risk Stratification Across Helicobacter pylori Infections With Diverse CagA Status and Subtypes in Brazil.

Luis Masuo Maruta, Asuka Furukawa, Heinrich Bender Kohnert Seidler, Aloisio Felipe-Silva, Keisuke Uchida, Daisuke Kobayashi, Kurara Yamamoto, Junko Minami, Masaki Sekine, Minako Takagi and 17 more

Abstract readValidation Study
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Prevention of Gastric Cancer.Medicina (Kaunas, Lithuania) · 2026
    Review
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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

27 authors.

Luis Masuo MarutaHospital Universitário, Endoscopy Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Asuka FurukawaDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.
Heinrich Bender Kohnert SeidlerLaboratório Brasiliense, Brasília, Distrito Federal, Brazil.
Aloisio Felipe-SilvaHospital Universitário, Anatomic Pathology Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Keisuke UchidaDivision of Surgical Pathology, Institute of Science Tokyo Hospital (Formerly Known as Tokyo Medical and Dental University Hospital), Tokyo, Japan.
Daisuke KobayashiDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.
Kurara YamamotoDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.
Junko MinamiDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.
Masaki SekineDivision of Surgical Pathology, Institute of Science Tokyo Hospital (Formerly Known as Tokyo Medical and Dental University Hospital), Tokyo, Japan.
Minako TakagiDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.
Renato Takayuki HassegawaHospital Universitário, Endoscopy Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Eduardo Koji Marchi OgawaHospital Japonês Santa Cruz, São Paulo, SP, Brazil.
Rodrigo Barbosa VillaçaClinica Brasília, Brasília, Distrito Federal, Brazil.
Tecio de Araujo CoutoClinica Brasília, Brasília, Distrito Federal, Brazil.
Jorge Alberto Capra BiasuzClinica Brasília, Brasília, Distrito Federal, Brazil.
Edmar TafnerHospital Universitário, Endoscopy Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Ana Luiza Werneck-SilvaHospital Universitário, Endoscopy Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Simone Perez PilliHospital Universitário, Endoscopy Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
José Guilherme Nogueira da SilvaHospital Universitário, Endoscopy Service, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Leonard Medeiros da SilvaHospital Japonês Santa Cruz, São Paulo, SP, Brazil.
Ricardo Ambrosio FockFaculty of Pharmaceutical Sciences, Universidade de São Paulo (USP), São Paulo, SP, Brazil.
Chinatsu OguraDivision of Surgical Pathology, Institute of Science Tokyo Hospital (Formerly Known as Tokyo Medical and Dental University Hospital), Tokyo, Japan.
Yumi MizuguchiDivision of Surgical Pathology, Institute of Science Tokyo Hospital (Formerly Known as Tokyo Medical and Dental University Hospital), Tokyo, Japan.
Keiko MiuraDivision of Surgical Pathology, Institute of Science Tokyo Hospital (Formerly Known as Tokyo Medical and Dental University Hospital), Tokyo, Japan.
Kouhei YamamotoDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.
Yoshinobu EishiDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.ORCID https://orcid.org/0000-0002-0521-1670
Kenichi OhashiDepartment of Human Pathology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo (Formerly Known as Tokyo Medical and Dental University), Tokyo, Japan.

Funding

Tokyo Medical and Dental University 11AA100346Tokyo Medical and Dental University 91AA191536
6 · The paper itself

Abstract

backgroundGastric cancer survival rates vary across countries due to differences in access to early diagnostic testing and healthcare quality. Endoscopy, though accurate, is not feasible for mass screening. The ABC method, which combines serum Helicobacter pylori (Hp) antibody and pepsinogen tests, has shown promise for gastric cancer risk stratification in Japan. However, its applicability in populations with diverse CagA status and subtypes remains uncertain. MATERIALS AND

methodsThis prospective study in Brazil evaluated the performance of the ABC method in an endoscopy-referred cohort with a heterogeneous distribution of Hp CagA status and subtypes. A recently validated immunohistochemical method was applied to formalin-fixed paraffin-embedded gastric biopsy samples to assess Hp infection, CagA expression, and CagA subtypes. Gastric pathology was evaluated using the updated Sydney System and OLGA/OLGIM staging and correlated with serum Hp antibody and pepsinogen levels in 586 patients, including 122 Japanese Brazilians.

resultsImmunohistochemistry achieved a 98% success rate (577/586). The prevalence of Hp infection was 48%, with Western-type CagA(+) (26%) and CagA(-) (18%) strains predominating. East Asian-type CagA(+) strains (4%) were observed primarily among Japanese Brazilians, particularly in second-generation individuals. Gastric pathology and serum markers differed significantly across CagA status and subtypes. Despite these differences, the ABC method's negative predictive values (NPVs) across all groups other than Group A (negative for both tests) remained high (97%/97% or 98%/100% for detecting OLGA/OLGIM stages ≥ II or ≥ III, and 94%/98% or 99%/100% for detecting antrum/corpus inflammation scores ≥ 2 or 3, respectively).

conclusionsThese findings demonstrate the clinical relevance of CagA diversity for gastric cancer risk assessment. Although limited to an endoscopy-referred cohort, the ABC method reliably identified low-risk individuals (Group A) and may help reduce unnecessary endoscopies in screening programs, regardless of CagA status and subtypes. Broader, population-based studies are needed to validate its generalizability and optimize its implementation.

Indexed as

Antigens, BacterialBacterial ProteinsHelicobacter InfectionsHelicobacter pyloriStomach NeoplasmsAdultAgedAntibodies, BacterialBrazilFemaleHumansImmunohistochemistryMaleMiddle AgedPepsinogen AProspective StudiesAntibodies, BacterialAntigens, BacterialBacterial ProteinscagA protein, Helicobacter pyloriPepsinogen AABC methodCagA subtypinggastric cancer risk stratificationHelicobacter pylori CagA diversityimmunohistochemistryintestinal metaplasiaintrafamilial transmissionnoninvasive screeningOLGA/OLGIM stagingserologic biomarkers

Identifiers

PMID40576027
PMCPMC12203232

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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 OpenQuestion graph.