Barrett Esophagus Length, Nodularity, and Low-grade Dysplasia are Predictive of Progression to Esophageal Adenocarcinoma.


Journal

Journal of clinical gastroenterology
ISSN: 1539-2031
Titre abrégé: J Clin Gastroenterol
Pays: United States
ID NLM: 7910017

Informations de publication

Date de publication:
Historique:
pubmed: 3 4 2018
medline: 21 8 2020
entrez: 3 4 2018
Statut: ppublish

Résumé

To investigate factors predictive of progression from nondysplastic Barrett esophagus (NDBE) or low-grade dysplasia (LGD) to high-grade dysplasia (HGD) or esophageal adenocarcinoma (EAC) using a large, prospective cohort of patients, wherein all esophageal biopsies undergo expert gastrointestinal pathologist review. Efficacy and cost-effectiveness of endoscopic surveillance to detect incident EAC in the setting of Barrett esophagus (BE), particularly in NDBE patients, is questioned. Previous studies have reported factors predictive of progression to EAC to guide surveillance intervals, but their strength is limited by small sample size and absence of expert gastrointestinal pathologist involvement in esophageal biopsy review. NDBE and LGD subjects were identified from a prospective registry in a tertiary care center. "Progressors" were BE subjects who developed HGD/EAC>12 months after the initial NDBE or LGD diagnosis. Cox proportional hazards model were used to identify predictors of progression. In total, 318 with NDBE and 301 with BE-LGD (mean age, 62.6 y, 85% male) were included. The mean follow-up was 5.3 years. The 7 NDBE and 21 LGD subjects progressed to HGD/EAC. BE length [hazards ratio (HR), 1.16; 95% confidence interval (CI), 1.03-1.29], presence of nodularity (HR, 4.98; 95% CI, 1.80-11.7), and baseline LGD (HR, 2.57; 95% CI, 1.13-6.57) were significant predictors of progression on multivariate analysis. In this well-defined cohort of NDBE and BE-LGD subjects, BE length, presence of LGD, and nodularity were independent predictors of progression to HGD/EAC. These factors may aid in identifying high-risk patients who may benefit from closer endoscopic surveillance/therapy.

Sections du résumé

GOALS
To investigate factors predictive of progression from nondysplastic Barrett esophagus (NDBE) or low-grade dysplasia (LGD) to high-grade dysplasia (HGD) or esophageal adenocarcinoma (EAC) using a large, prospective cohort of patients, wherein all esophageal biopsies undergo expert gastrointestinal pathologist review.
BACKGROUND
Efficacy and cost-effectiveness of endoscopic surveillance to detect incident EAC in the setting of Barrett esophagus (BE), particularly in NDBE patients, is questioned. Previous studies have reported factors predictive of progression to EAC to guide surveillance intervals, but their strength is limited by small sample size and absence of expert gastrointestinal pathologist involvement in esophageal biopsy review.
STUDY
NDBE and LGD subjects were identified from a prospective registry in a tertiary care center. "Progressors" were BE subjects who developed HGD/EAC>12 months after the initial NDBE or LGD diagnosis. Cox proportional hazards model were used to identify predictors of progression.
RESULTS
In total, 318 with NDBE and 301 with BE-LGD (mean age, 62.6 y, 85% male) were included. The mean follow-up was 5.3 years. The 7 NDBE and 21 LGD subjects progressed to HGD/EAC. BE length [hazards ratio (HR), 1.16; 95% confidence interval (CI), 1.03-1.29], presence of nodularity (HR, 4.98; 95% CI, 1.80-11.7), and baseline LGD (HR, 2.57; 95% CI, 1.13-6.57) were significant predictors of progression on multivariate analysis.
CONCLUSIONS
In this well-defined cohort of NDBE and BE-LGD subjects, BE length, presence of LGD, and nodularity were independent predictors of progression to HGD/EAC. These factors may aid in identifying high-risk patients who may benefit from closer endoscopic surveillance/therapy.

Identifiants

pubmed: 29608452
doi: 10.1097/MCG.0000000000001027
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

361-365

Auteurs

Dipesh Solanky (D)

Mayo Clinic School of Medicine School.

Rajesh Krishnamoorthi (R)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Nicholas Crews (N)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Michele Johnson (M)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Kenneth Wang (K)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Herbert Wolfsen (H)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL.

David Fleischer (D)

Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, AZ.

Francisco C Ramirez (FC)

Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, AZ.

David Katzka (D)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Navtej Buttar (N)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

Prasad G Iyer (PG)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.

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