Vertical R1 margins are not always associated with residual neoplasia after endoscopic resection of Barrett's neoplasia: a nationwide cohort with dedicated pathology reassessment.


Journal

Endoscopy
ISSN: 1438-8812
Titre abrégé: Endoscopy
Pays: Germany
ID NLM: 0215166

Informations de publication

Date de publication:
20 Feb 2024
Historique:
medline: 21 2 2024
pubmed: 21 2 2024
entrez: 20 2 2024
Statut: aheadofprint

Résumé

To evaluate the proportion of patients with residual neoplasia after endoscopic resection (ER) for Barrett's neoplasia with confirmed tumor-positive vertical resection margin (R1v). Retrospective cohort study including all patients treated with ER for Barrett's neoplasia with histologically documented R1v since 2008 in the Dutch Barrett Expert Centers. R1v was defined as cancer cells touching the vertical resection margin and Rx as not assessable margins. Reassessment of R1v specimen was performed by experienced pathologists until consensus was reached regarding vertical margins. 101/110 included patients had macroscopically complete resections (T1a n=17, T1b n=84), of which 99/101 (98%) ER specimens were reassessed. Reassessment confirmed R1v in 74 (75%) patients and found Rx in 16% and R0 in 9%. Presence of residual neoplasia could be assessed in 66/74 patients during endoscopic reassessment (n=52) and/or in the surgical resection specimen (n=14), of whom 33/66 (50%)had residual neoplasia. Residual neoplasia detected during endoscopy was always endoscopically visible and biopsies from a normal appearing ER-scar did not detect additional neoplasia. Twenty-five patients with no residual neoplasia during endoscopic reassessment underwent endoscopic follow-up for median 37 months(IQR 12-50), in which 4 developed a local recurrence(16.0%), all detected as visible abnormalities. Histological evaluation of ER margins appears challenging as 75% of documented R1v cases were confirmed during reassessment. After ER with R1v, 50% of the patients had no residual neoplasia. Endoscopic reassessment 8-12 weeks after ER seems accurately able to detect residual neoplasia and help to determine the most appropriate strategy for patients with R1v.

Sections du résumé

BACKGROUND BACKGROUND
To evaluate the proportion of patients with residual neoplasia after endoscopic resection (ER) for Barrett's neoplasia with confirmed tumor-positive vertical resection margin (R1v).
METHODS METHODS
Retrospective cohort study including all patients treated with ER for Barrett's neoplasia with histologically documented R1v since 2008 in the Dutch Barrett Expert Centers. R1v was defined as cancer cells touching the vertical resection margin and Rx as not assessable margins. Reassessment of R1v specimen was performed by experienced pathologists until consensus was reached regarding vertical margins.
RESULTS RESULTS
101/110 included patients had macroscopically complete resections (T1a n=17, T1b n=84), of which 99/101 (98%) ER specimens were reassessed. Reassessment confirmed R1v in 74 (75%) patients and found Rx in 16% and R0 in 9%. Presence of residual neoplasia could be assessed in 66/74 patients during endoscopic reassessment (n=52) and/or in the surgical resection specimen (n=14), of whom 33/66 (50%)had residual neoplasia. Residual neoplasia detected during endoscopy was always endoscopically visible and biopsies from a normal appearing ER-scar did not detect additional neoplasia. Twenty-five patients with no residual neoplasia during endoscopic reassessment underwent endoscopic follow-up for median 37 months(IQR 12-50), in which 4 developed a local recurrence(16.0%), all detected as visible abnormalities.
CONCLUSIONS CONCLUSIONS
Histological evaluation of ER margins appears challenging as 75% of documented R1v cases were confirmed during reassessment. After ER with R1v, 50% of the patients had no residual neoplasia. Endoscopic reassessment 8-12 weeks after ER seems accurately able to detect residual neoplasia and help to determine the most appropriate strategy for patients with R1v.

Identifiants

pubmed: 38378018
doi: 10.1055/a-2272-9794
doi:

Types de publication

Clinical Trial

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).

Déclaration de conflit d'intérêts

Bas LAM Weusten Pentax Medical: financial research support, lecture fees, consultancy. Aqua Medical: financial research support. Roos E Pouw: Consultancy for Medtronic BV and MicroTech Europe, Speaker fee for Pentax. The remaining coauthors have no conflict of interest.

Auteurs

Laurelle van Tilburg (L)

Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, Netherlands.

Eva Verheij (E)

Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism, Cancer Center Amsterdam, Amsterdam, Netherlands.

Steffi Elisabeth Maria van de Ven (SEM)

Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, Netherlands.

Sanne van Munster (S)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism, Cancer Center Amsterdam, Amsterdam, Netherlands.

Bas Weusten (B)

Gastroenterology and Hepatology, University Medical Centre Utrecht, Utrecht, Netherlands.
Gastroenterology and Hepatology, St. Antonius Hospital, Nieuwegein, Netherlands.

Lorenza Alvarez Herrero (L)

Gastroenterology and Hepatology, St. Antonius Hospital, Nieuwegein, Netherlands.

Wouter B Nagengast (WB)

Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.

Erik J Schoon (EJ)

Gastroenterology and Hepatology, Catharina Hospital, Catharina Cancer Institute, Eindhoven, Netherlands.
GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, Netherlands.

Alaa Alkhalaf (A)

Gastroenterology and Hepatology, Isala Clinics, Zwolle, Netherlands.

Jacques Bergman (J)

Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism, Cancer Center Amsterdam, Amsterdam, Netherlands.

Roos E Pouw (RE)

Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism, Cancer Center Amsterdam, Amsterdam, Netherlands.

Lindsey Oudijk (L)

Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, Netherlands.

Sybren L Meijer (SL)

Pathology, Amsterdam University Medical Centres, Amsterdam, Netherlands.

Marnix Jansen (M)

Pathology, University College London Hospitals NHS Foundation Trust, London, United Kingdom of Great Britain and Northern Ireland.
Pathology, University College London Cancer Institute, London, United Kingdom of Great Britain and Northern Ireland.

Michael Doukas (M)

Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, Netherlands.

Arjun Dave Koch (AD)

Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, Netherlands.

Classifications MeSH