Nonrecurrence Rate of Underwater EMR for ≤20-mm Nonampullary Duodenal Adenomas: A Multicenter Prospective Study (D-UEMR Study).
Duodenal Adenoma
Follow-Up
Nonrecurrence Rate
Underwater Endoscopic Mucosal Resection
Journal
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775
Informations de publication
Date de publication:
05 2022
05 2022
Historique:
received:
24
06
2021
accepted:
25
06
2021
pubmed:
5
7
2021
medline:
20
4
2022
entrez:
4
7
2021
Statut:
ppublish
Résumé
Endoscopic resection of nonampullary duodenal adenoma is often challenging, and its technique has not yet been standardized. To overcome the practical difficulty of conventional endoscopic mucosal resection, underwater endoscopic mucosal resection (UEMR) was recently developed; therefore, we investigated the effectiveness and safety of UEMR for nonampullary duodenal adenoma. A multicenter, prospective cohort study was conducted at 21 institutions in Japan. We enrolled patients with no more than 2 nonampullary duodenal adenomas ≤20 mm in size, who were planned to undergo UEMR. After UEMR, follow-up endoscopies were scheduled at 2 and 12 months after the procedure, and biopsy specimens were taken from the post-UEMR scars. The primary endpoint was the proportion of patients with histologically proven nonrecurrence at follow-up endoscopy and biopsy. A total of 155 patients with 166 lesions underwent UEMR. One patient with a non-neoplastic lesion in the resected specimen and 10 patients with 10 lesions who were lost to follow-up were excluded. Finally, 144 patients with 155 lesions who received all follow-up endoscopies were analyzed for the primary endpoint. The proportion of patients with proven nonrecurrence was 97.2% (n = 140 of 144; 95% confidence interval, 92.8%-99.1%) which exceeded the predefined threshold value (92%). Two cases of delayed bleeding (1.2%) occurred and they were successfully managed by clips. All recurrences were successfully treated by additional endoscopic treatment. This multicenter, prospective cohort study demonstrated effectiveness and safety of UEMR for nonampullary duodenal adenomas ≤20 mm in size. (University Hospital Medical Network Clinical Trials Registry, Number: UMIN000030414).
Sections du résumé
BACKGROUND AND AIMS
Endoscopic resection of nonampullary duodenal adenoma is often challenging, and its technique has not yet been standardized. To overcome the practical difficulty of conventional endoscopic mucosal resection, underwater endoscopic mucosal resection (UEMR) was recently developed; therefore, we investigated the effectiveness and safety of UEMR for nonampullary duodenal adenoma.
METHODS
A multicenter, prospective cohort study was conducted at 21 institutions in Japan. We enrolled patients with no more than 2 nonampullary duodenal adenomas ≤20 mm in size, who were planned to undergo UEMR. After UEMR, follow-up endoscopies were scheduled at 2 and 12 months after the procedure, and biopsy specimens were taken from the post-UEMR scars. The primary endpoint was the proportion of patients with histologically proven nonrecurrence at follow-up endoscopy and biopsy.
RESULTS
A total of 155 patients with 166 lesions underwent UEMR. One patient with a non-neoplastic lesion in the resected specimen and 10 patients with 10 lesions who were lost to follow-up were excluded. Finally, 144 patients with 155 lesions who received all follow-up endoscopies were analyzed for the primary endpoint. The proportion of patients with proven nonrecurrence was 97.2% (n = 140 of 144; 95% confidence interval, 92.8%-99.1%) which exceeded the predefined threshold value (92%). Two cases of delayed bleeding (1.2%) occurred and they were successfully managed by clips. All recurrences were successfully treated by additional endoscopic treatment.
CONCLUSIONS
This multicenter, prospective cohort study demonstrated effectiveness and safety of UEMR for nonampullary duodenal adenomas ≤20 mm in size. (University Hospital Medical Network Clinical Trials Registry, Number: UMIN000030414).
Identifiants
pubmed: 34217879
pii: S1542-3565(21)00707-2
doi: 10.1016/j.cgh.2021.06.043
pii:
doi:
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
1010-1018.e3Investigateurs
Hiromitsu Kanzaki
(H)
Shuntaro Inoue
(S)
Muneaki Miyake
(M)
Masayasu Ohmori
(M)
Yoji Takeuchi
(Y)
Yasuhiro Tani
(Y)
Nobuyuki Harada
(N)
Nobukazu Agatsuma
(N)
Keijirou Okada
(K)
Maiko Ikenouchi
(M)
Yasuki Nakatani
(Y)
Yoshito Uenoyama
(Y)
Yukitaka Yamashita
(Y)
Shigenao Ishikawa
(S)
Tomoki Inaba
(T)
Koji Miyahara
(K)
Yuki Moritou
(Y)
Masahiro Nakagawa
(M)
Hiroaki Kitae
(H)
Tsugitaka Ishida
(T)
Yuji Naito
(Y)
Akiyoshi Nishio
(A)
Masaaki Shimatani
(M)
Ryo Kato
(R)
Shinya Taki
(S)
Koichiro Mandai
(K)
Kasumi Sanada
(K)
Kojiro Nakase
(K)
Hiroko Nebiki
(H)
Shunsuke Saito
(S)
Toshiyuki Wakatsuki
(T)
Naoyuki Nishimura
(N)
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2022 AGA Institute. Published by Elsevier Inc. All rights reserved.