Epidemiology and Outcomes of Young-Onset Esophageal Adenocarcinoma: An Analysis from a Population-Based Database.


Journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608

Informations de publication

Date de publication:
01 2021
Historique:
received: 23 06 2020
revised: 20 08 2020
accepted: 05 10 2020
pubmed: 18 12 2020
medline: 27 11 2021
entrez: 17 12 2020
Statut: ppublish

Résumé

Esophageal adenocarcinoma is a lethal cancer with rising incidence. There are limited data in younger (<50 years) patients with esophageal adenocarcinoma. We aimed to assess time trends in the incidence and outcomes of "young-onset" esophageal adenocarcinoma using a population-based database. We queried the Surveillance, Epidemiology, and End Results 9 database to identify patients with esophageal adenocarcinoma between 1975 and 2015. Patients were stratified into three age strata: <50, 50 to 69, and ≥70 years. Staging was stratified as localized, regional, and distant. Trends in incidence, disease stage, and survival were assessed in three periods (1975-89, 1990-99, and 2000-2015). Univariate and multivariate models were created to identify predictors of mortality. Esophageal adenocarcinoma incidence has increased in patients <50 years of age, with an annual percentage change of 2.9% (95% confidence interval, 1.4%-4.4%) from 1975 to 2015. Young-onset esophageal adenocarcinoma presented at more advanced stages (regional + distant) compared with older patients (84.9% vs. 67.3%; Young-onset esophageal adenocarcinoma, while uncommon, is rising in incidence. Concerningly, the proportion of advanced disease continues to increase. Young-onset esophageal adenocarcinoma also presents at more advanced stages, resulting in poorer esophageal adenocarcinoma-free survival. Patients with esophageal adenocarcinoma younger than 50 years present at more advanced stages with higher esophageal adenocarcinoma-specific mortality compared with older peers. Current diagnostic and management strategies for young-onset esophageal adenocarcinoma may need to be reevaluated.

Sections du résumé

BACKGROUND
Esophageal adenocarcinoma is a lethal cancer with rising incidence. There are limited data in younger (<50 years) patients with esophageal adenocarcinoma. We aimed to assess time trends in the incidence and outcomes of "young-onset" esophageal adenocarcinoma using a population-based database.
METHODS
We queried the Surveillance, Epidemiology, and End Results 9 database to identify patients with esophageal adenocarcinoma between 1975 and 2015. Patients were stratified into three age strata: <50, 50 to 69, and ≥70 years. Staging was stratified as localized, regional, and distant. Trends in incidence, disease stage, and survival were assessed in three periods (1975-89, 1990-99, and 2000-2015). Univariate and multivariate models were created to identify predictors of mortality.
RESULTS
Esophageal adenocarcinoma incidence has increased in patients <50 years of age, with an annual percentage change of 2.9% (95% confidence interval, 1.4%-4.4%) from 1975 to 2015. Young-onset esophageal adenocarcinoma presented at more advanced stages (regional + distant) compared with older patients (84.9% vs. 67.3%;
CONCLUSIONS
Young-onset esophageal adenocarcinoma, while uncommon, is rising in incidence. Concerningly, the proportion of advanced disease continues to increase. Young-onset esophageal adenocarcinoma also presents at more advanced stages, resulting in poorer esophageal adenocarcinoma-free survival.
IMPACT
Patients with esophageal adenocarcinoma younger than 50 years present at more advanced stages with higher esophageal adenocarcinoma-specific mortality compared with older peers. Current diagnostic and management strategies for young-onset esophageal adenocarcinoma may need to be reevaluated.

Identifiants

pubmed: 33328255
pii: 1055-9965.EPI-20-0944
doi: 10.1158/1055-9965.EPI-20-0944
pmc: PMC7855414
mid: NIHMS1637234
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

142-149

Subventions

Organisme : NCI NIH HHS
ID : R01 CA241164
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002377
Pays : United States

Informations de copyright

©2020 American Association for Cancer Research.

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Auteurs

Don C Codipilly (DC)

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

Tarek Sawas (T)

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

Lovekirat Dhaliwal (L)

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

Michele L Johnson (ML)

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

Ramona Lansing (R)

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

Kenneth K Wang (KK)

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

Cadman L Leggett (CL)

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

David A Katzka (DA)

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

Prasad G Iyer (PG)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. iyer.prasad@mayo.edu.

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