Prognostic Impact of the Presence of Barrett's Esophagus and Intestinal Metaplasia on Esophageal Adenocarcinoma Survival.

Barrett’s esophagus esophageal adenocarcinoma intestinal metaplasia

Journal

Foregut (Thousand Oaks, Calif.)
ISSN: 2634-5161
Titre abrégé: Foregut
Pays: United States
ID NLM: 9918266300406676

Informations de publication

Date de publication:
Dec 2022
Historique:
entrez: 29 12 2022
pubmed: 30 12 2022
medline: 30 12 2022
Statut: ppublish

Résumé

Barrett's esophagus (BE), defined by the presence of intestinal metaplasia (IM) on histology, is thought to be the only identifiable precursor lesion for esophageal adenocarcinoma (EAC). Recent studies have suggested the possibility of an alternate, non-IM associated EAC that is a more aggressive form of EAC with worse survival. Among EAC patients, we aimed to compare survival of patients with and without IM at the time of diagnosis. This was a retrospective cohort study of all patients with histologic confirmed EAC evaluated at a tertiary care center from 2013 to 2019. Cases were categorized according to the presence or absence of IM on histologic specimens (Group I-IM-EAC and Group II-non-IM-EAC). We compared demographic characteristics, clinical stage, therapy, and survival between the 2 groups using the Chi-square and ANOVA tests (for categorical and continuous variables, respectively). We used Cox proportional hazards regression to determine the association of IM with overall survival, adjusting for sex, age at diagnosis, tumor location, histologic grade, and clinical stage. A total of 475 patients were included in this analysis (mean age 64.8 years [SD 10.8], 89% white) and 109 (23.0%) had no evidence of IM. Compared with IM-EAC (Group I), individuals in the non-IM-EAC group were younger ( EAC without the presence of IM on histology was associated with worse survival compared to those with IM. Future prospective studies with detailed molecular sequencing are required to clarify if 2 separate phenotypes of EAC exist (IM-EAC and non-IM-EAC). If confirmed, this may have significant implications for screening and management strategies.

Sections du résumé

Background/Aims UNASSIGNED
Barrett's esophagus (BE), defined by the presence of intestinal metaplasia (IM) on histology, is thought to be the only identifiable precursor lesion for esophageal adenocarcinoma (EAC). Recent studies have suggested the possibility of an alternate, non-IM associated EAC that is a more aggressive form of EAC with worse survival. Among EAC patients, we aimed to compare survival of patients with and without IM at the time of diagnosis.
Methods UNASSIGNED
This was a retrospective cohort study of all patients with histologic confirmed EAC evaluated at a tertiary care center from 2013 to 2019. Cases were categorized according to the presence or absence of IM on histologic specimens (Group I-IM-EAC and Group II-non-IM-EAC). We compared demographic characteristics, clinical stage, therapy, and survival between the 2 groups using the Chi-square and ANOVA tests (for categorical and continuous variables, respectively). We used Cox proportional hazards regression to determine the association of IM with overall survival, adjusting for sex, age at diagnosis, tumor location, histologic grade, and clinical stage.
Results UNASSIGNED
A total of 475 patients were included in this analysis (mean age 64.8 years [SD 10.8], 89% white) and 109 (23.0%) had no evidence of IM. Compared with IM-EAC (Group I), individuals in the non-IM-EAC group were younger (
Conclusions UNASSIGNED
EAC without the presence of IM on histology was associated with worse survival compared to those with IM. Future prospective studies with detailed molecular sequencing are required to clarify if 2 separate phenotypes of EAC exist (IM-EAC and non-IM-EAC). If confirmed, this may have significant implications for screening and management strategies.

Identifiants

pubmed: 36578279
doi: 10.1177/26345161211033277
pmc: PMC9793872
mid: NIHMS1816383
doi:

Types de publication

Journal Article

Langues

eng

Pagination

356-364

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK007038
Pays : United States

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Auteurs

Jennifer M Kolb (JM)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Charlie Fox (C)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Chloe Friedman (C)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Frank I Scott (FI)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Samuel Han (S)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Megan Marsh (M)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Martin McCarter (M)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Jeffrey Kaplan (J)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Christopher H Lieu (CH)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Ana Gleisner (A)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

David A Katzka (DA)

Mayo Clinic Rochester, Rochester, MN, USA.

Sachin Wani (S)

University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Classifications MeSH