Clinical Outcomes After Endoscopic Management of Low-Risk and High-Risk T1a Esophageal Adenocarcinoma: A Multicenter Study

Author:

Kamboj Amrit K.1ORCID,Goyal Rohit1,Vantanasiri Kornpong1ORCID,Sachdeva Karan1,Passe Melissa1,Lansing Ramona1,Garg Nikita1,Chandi Paras S.1ORCID,Ramirez Francisco C.2,Kahn Allon2ORCID,Fukami Norio2ORCID,Wolfsen Herbert C.3,Krishna Murli4,Pai Rish K.5ORCID,Hagen Catherine6,Lee Hee Eun6,Wang Kenneth K.1,Leggett Cadman L.1ORCID,Iyer Prasad G.1

Affiliation:

1. Barrett's Esophagus Unit, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA;

2. Barrett's Esophagus Unit, Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona, USA;

3. Barrett's Esophagus Unit, Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA;

4. Department of Pathology, Mayo Clinic, Jacksonville, Florida, USA;

5. Department of Pathology, Mayo Clinic, Scottsdale, Arizona, USA;

6. Department of Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Abstract

INTRODUCTION: Endoscopic eradication therapy (EET) is standard of care for T1a esophageal adenocarcinoma (EAC). However, data on outcomes in high-risk T1a EAC are limited. We assessed and compared outcomes after EET of low-risk and high-risk T1a EAC, including intraluminal EAC recurrence, extraesophageal metastases, and overall survival. METHODS: Patients who underwent EET for T1a EAC at 3 referral Barrett's esophagus endotherapy units between 1996 and 2022 were included. Patients with submucosal invasion, positive deep margins, or metastases at initial diagnosis were excluded. High-risk T1a EAC was defined as T1a EAC with poor differentiation and/or lymphovascular invasion, with low-risk disease being defined without these features. All pathology was systematically assessed by expert gastrointestinal pathologists. Baseline and follow-up endoscopy and pathology data were abstracted. Time-to-event analyses were performed to compare outcomes between groups. RESULTS: One hundred eighty-eight patients with T1a EAC were included (high risk, n = 45; low risk, n = 143) with a median age of 70 years, and 84% were men. Groups were comparable for age, sex, Barrett's esophagus length, lesion size, and EET technique. Rates of delayed extraesophageal metastases (11.1% vs 1.4%) were significantly higher in the high-risk group (P = 0.02). There was no significant difference in the rates of intraluminal EAC recurrence (P = 0.79) and overall survival (P = 0.73) between the 2 groups. DISCUSSION: Patients with high-risk T1a EAC undergoing successful EET had a substantially higher rate of extraesophageal metastases compared with those with low-risk T1a EAC on long-term follow-up. These data should be factored into discussions with patients while selecting treatment approaches. Additional prospective data in this area are critical.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

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