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The Colombian Chemoprevention Trial: 20-Year Follow-Up of a Cohort of Patients With Gastric Precancerous Lesions.
Piazuelo, M Blanca; Bravo, Luis E; Mera, Robertino M; Camargo, M Constanza; Bravo, Juan C; Delgado, Alberto G; Washington, M Kay; Rosero, Alicia; Garcia, Luz S; Realpe, Jose L; Cifuentes, Sandra P; Morgan, Douglas R; Peek, Richard M; Correa, Pelayo; Wilson, Keith T.
Afiliação
  • Piazuelo MB; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Center for Mucosal Inflammation and Cancer, Vanderbilt University Medical Center, Nashville, Tennessee. Electronic address: maria.b.piazuelo@vumc.org.
  • Bravo LE; Department of Pathology, Universidad del Valle School of Medicine, Cali, Valle del Cauca, Colombia.
  • Mera RM; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Camargo MC; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
  • Bravo JC; Department of Pathology, Universidad del Valle School of Medicine, Cali, Valle del Cauca, Colombia.
  • Delgado AG; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Washington MK; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Rosero A; Universidad de Nariño, Pasto, Nariño, Colombia.
  • Garcia LS; Department of Pathology, Universidad del Valle School of Medicine, Cali, Valle del Cauca, Colombia.
  • Realpe JL; Fundación Hospital San Pedro, Pasto, Nariño, Colombia.
  • Cifuentes SP; Fundación Hospital San Pedro, Pasto, Nariño, Colombia.
  • Morgan DR; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Division of Gastroenterology, Department of Medicine, University of Alabama, Birmingham, Alabama.
  • Peek RM; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Center for Mucosal Inflammation and Cancer, Vanderbilt University Medical Center, Nashville, Tennessee; Department of Pathology, Microbiology and Immunology, V
  • Correa P; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Wilson KT; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee; Center for Mucosal Inflammation and Cancer, Vanderbilt University Medical Center, Nashville, Tennessee; Department of Pathology, Microbiology and Immunology, V
Gastroenterology ; 160(4): 1106-1117.e3, 2021 03.
Article em En | MEDLINE | ID: mdl-33220252
ABSTRACT
BACKGROUND &

AIMS:

Helicobacter pylori eradication and endoscopic surveillance of gastric precancerous lesions are strategies to reduce gastric cancer (GC) risk. To our knowledge, this study is the longest prospective cohort of an H pylori eradication trial in a Hispanic population.

METHODS:

A total of 800 adults with precancerous lesions were randomized to anti-H pylori treatment or placebo. Gastric biopsy samples taken at baseline and 3, 6, 12, 16, and 20 years were assessed by our Correa histopathology score. A generalized linear mixed model with a participant-level random intercept was used to estimate the effect of H pylori status on the score over time. Logistic regression models were used to estimate progression by baseline diagnosis and to estimate GC risk by intestinal metaplasia (IM) subtype and anatomic location.

RESULTS:

Overall, 356 individuals completed 20 years of follow-up. Anti-H pylori therapy (intention-to-treat) reduced progression of the Correa score (odds ratio [OR], 0.59; 95% confidence interval [CI], 0.38-0.93). H pylori-negative status had a beneficial effect on the score over time (P = .036). Among individuals with IM (including indefinite for dysplasia) at baseline, incidence rates per 100 person-years were 1.09 (95% CI, 0.85-1.33) for low-grade/high-grade dysplasia and 0.14 (95% CI, 0.06-0.22) for GC. Incomplete-type (vs complete-type) IM at baseline presented higher GC risk (OR, 13.4; 95% CI, 1.8-103.8). Individuals with corpus (vs antrum-restricted) IM showed an OR of 2.1 (95% CI, 0.7-6.6) for GC.

CONCLUSIONS:

In a high-GC-risk Hispanic population, anti-H pylori therapy had a long-term beneficial effect against histologic progression. Incomplete IM is a strong predictor of GC risk.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Neoplasias Gástricas / Infecções por Helicobacter / Mucosa Gástrica / Antibacterianos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País como assunto: America do sul / Colombia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Neoplasias Gástricas / Infecções por Helicobacter / Mucosa Gástrica / Antibacterianos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País como assunto: America do sul / Colombia Idioma: En Ano de publicação: 2021 Tipo de documento: Article