TY - JOUR
T1 - Limitations of Heartburn and Other Societies’ Criteria in Barrett's Screening for Detecting De Novo Esophageal Adenocarcinoma
AU - Sawas, Tarek
AU - Zamani, Shawn A.
AU - Killcoyne, Sarah
AU - Dullea, Andrew
AU - Wang, Kenneth K.
AU - Iyer, Prasad G.
AU - Fitzgerald, Rebecca C.
AU - Katzka, David A.
N1 - Funding Information:
Tarek Sawas (Data curation: Equal; Formal analysis: Equal; Methodology: Equal; Writing ? original draft: Equal), Shawn A. Zamani (Data curation: Equal; Formal analysis: Equal; Methodology: Equal; Writing ? original draft: Equal), Sarah Killcoyne (Investigation: Equal; Methodology: Equal; Writing ? original draft: Equal), Andrew Dullea (Methodology: Supporting; Writing ? original draft: Supporting), Kenneth K. Wang (Writing ? review & editing: Supporting), Prasad G. Iyer (Methodology: Supporting; Writing ? review & editing: Supporting), Rebecca C. Fitzgerald (Conceptualization: Equal; Investigation: Equal; Methodology: Equal; Supervision: Equal; Writing ? original draft: Equal; Writing ? review & editing: Equal), David A. Katzka (Conceptualization: Equal; Investigation: Equal; Supervision: Equal; Writing ? original draft: Equal; Writing ? review & editing: Equal)
Publisher Copyright:
© 2021 AGA Institute
PY - 2021
Y1 - 2021
N2 - Background & Aims: Despite extensive Barrett's esophagus (BE) screening efforts, most patients with esophageal adenocarcinoma (EAC) present de novo. It is unclear how much of this problem is the result of insensitivity or poor applications of current screening guidelines. We aimed to evaluate the sensitivity of guidelines by determining the proportion of prevalent EAC cases that meet the American College of Gastroenterology (ACG) or the British Society of Gastroenterology (BSG) guidelines for BE screening and determine whether changes to criteria would enhance detection. Methods: A retrospective single-center cohort from the United States (n = 663) and a prospective multicenter cohort from the United Kingdom (n = 645) were collected and analyzed independently. Screening eligibility was determined as patients with chronic reflux and at least 2 or more risk factors as defined by the guidelines. We calculated the proportion of screening-eligible patients and then compared BE/EAC risk factors between screening-eligible and screening-ineligible patients using the chi-squared or Student t test as appropriate. Results: In the Mayo clinic cohort there were 54.9% EAC cases and in the UK cohort there were 38.9% EAC cases that were not identified by ACG or BSG screening criteria, respectively. Among patients who did not meet the screening criteria, lack of heartburn was observed in 86.5% in the Mayo clinic cohort and in 61.4% in the UK cohort. Other risk factors that were lacking included obesity (defined as a body mass index of ≥30 kg/m2) and family history of EAC. Eliminating chronic reflux from the ACG/BSG criteria improved eligibility for screening from 45.1% to 81.3% (P < .001) in the Mayo Clinic cohort and from 61.1% (n = 394) to 81.5% (n = 526; P < .001) in the UK cohort. However, reflux may be difficult to ascertain from the history, and by including proton pump inhibitor use status in addition to the BSG criteria, screening eligibility improved by 10.0% in the UK cohort (n = 459; P < .001). Conclusions: ACG/BSG BE screening guidelines have limited our ability to detect prevalent EAC. An optimized approach to identifying the individuals most suitable for EAC screening needs to be implemented, particularly one that does not rely on chronic reflux symptoms.
AB - Background & Aims: Despite extensive Barrett's esophagus (BE) screening efforts, most patients with esophageal adenocarcinoma (EAC) present de novo. It is unclear how much of this problem is the result of insensitivity or poor applications of current screening guidelines. We aimed to evaluate the sensitivity of guidelines by determining the proportion of prevalent EAC cases that meet the American College of Gastroenterology (ACG) or the British Society of Gastroenterology (BSG) guidelines for BE screening and determine whether changes to criteria would enhance detection. Methods: A retrospective single-center cohort from the United States (n = 663) and a prospective multicenter cohort from the United Kingdom (n = 645) were collected and analyzed independently. Screening eligibility was determined as patients with chronic reflux and at least 2 or more risk factors as defined by the guidelines. We calculated the proportion of screening-eligible patients and then compared BE/EAC risk factors between screening-eligible and screening-ineligible patients using the chi-squared or Student t test as appropriate. Results: In the Mayo clinic cohort there were 54.9% EAC cases and in the UK cohort there were 38.9% EAC cases that were not identified by ACG or BSG screening criteria, respectively. Among patients who did not meet the screening criteria, lack of heartburn was observed in 86.5% in the Mayo clinic cohort and in 61.4% in the UK cohort. Other risk factors that were lacking included obesity (defined as a body mass index of ≥30 kg/m2) and family history of EAC. Eliminating chronic reflux from the ACG/BSG criteria improved eligibility for screening from 45.1% to 81.3% (P < .001) in the Mayo Clinic cohort and from 61.1% (n = 394) to 81.5% (n = 526; P < .001) in the UK cohort. However, reflux may be difficult to ascertain from the history, and by including proton pump inhibitor use status in addition to the BSG criteria, screening eligibility improved by 10.0% in the UK cohort (n = 459; P < .001). Conclusions: ACG/BSG BE screening guidelines have limited our ability to detect prevalent EAC. An optimized approach to identifying the individuals most suitable for EAC screening needs to be implemented, particularly one that does not rely on chronic reflux symptoms.
KW - Barrett's Esophagus Screening
KW - Esophageal Adenocarcinoma
KW - Gastroesophageal Reflux Disease
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U2 - 10.1016/j.cgh.2021.10.039
DO - 10.1016/j.cgh.2021.10.039
M3 - Article
C2 - 34757196
AN - SCOPUS:85121240335
SN - 1542-3565
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
ER -