Long-term outcomes after endoscopic submucosal dissection for differentiated-type early gastric cancer that fulfilled expanded indication criteria: A prospective cohort study.


Journal

Journal of gastroenterology and hepatology
ISSN: 1440-1746
Titre abrégé: J Gastroenterol Hepatol
Pays: Australia
ID NLM: 8607909

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 25 11 2019
revised: 21 06 2020
accepted: 27 06 2020
pubmed: 15 7 2020
medline: 26 8 2021
entrez: 15 7 2020
Statut: ppublish

Résumé

Endoscopic resection for early gastric cancer (EGC) is widely performed. However, there is still a paucity of strong evidence regarding long-term outcomes after endoscopic submucosal dissection (ESD) for the expanded indication criteria of the Japanese guidelines (ver. 2010). Endoscopic submucosal dissection was performed in patients with EGC that met the expanded indication criteria: (i) cT1a, differentiated-type EGC of 2 to 5 cm, ulcer negative or (ii) cT1a, differentiated-type EGC of ≤3 cm, ulcer positive. Patients whose pathological examination fulfilled the curative resection criteria were then enrolled in this cohort study: negative vertical margin, negative lymphovascular invasion, and (i) pT1a, differentiated-type, and ulcer negative; (ii) pT1a, differentiated-type, ≤3 cm, and ulcer positive; or (iii) pT1b1 (<500-μm submucosal invasion), differentiated-type, and ≤3 cm. Patients with only a positive horizontal margin as a noncurative factor were included for follow-up. From September 2003 to February 2012, a total of 356 patients underwent ESD, and 214 were enrolled in the survival analysis. One hundred twenty patients (56%) had >2 cm in diameter and ulcer-negative lesions, and 94 (44%) had ≤3 cm and ulcer-positive lesions. The vital status at 5 years after ESD was confirmed in all (100%) patients. No local or metastatic recurrence was detected; however, 26 metachronous gastric cancers developed, and 1 patient died of metachronous gastric cancer. The 5-year disease-specific and overall survival rates were 99.5% (95% confidence interval [CI], 97.2%-100%) and 93.9% (95% CI, 89.8%-96.4%), respectively. ESD for EGC that fulfills the expanded criteria is feasible and shows favorable long-term outcomes.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Endoscopic resection for early gastric cancer (EGC) is widely performed. However, there is still a paucity of strong evidence regarding long-term outcomes after endoscopic submucosal dissection (ESD) for the expanded indication criteria of the Japanese guidelines (ver. 2010).
METHODS METHODS
Endoscopic submucosal dissection was performed in patients with EGC that met the expanded indication criteria: (i) cT1a, differentiated-type EGC of 2 to 5 cm, ulcer negative or (ii) cT1a, differentiated-type EGC of ≤3 cm, ulcer positive. Patients whose pathological examination fulfilled the curative resection criteria were then enrolled in this cohort study: negative vertical margin, negative lymphovascular invasion, and (i) pT1a, differentiated-type, and ulcer negative; (ii) pT1a, differentiated-type, ≤3 cm, and ulcer positive; or (iii) pT1b1 (<500-μm submucosal invasion), differentiated-type, and ≤3 cm. Patients with only a positive horizontal margin as a noncurative factor were included for follow-up.
RESULTS RESULTS
From September 2003 to February 2012, a total of 356 patients underwent ESD, and 214 were enrolled in the survival analysis. One hundred twenty patients (56%) had >2 cm in diameter and ulcer-negative lesions, and 94 (44%) had ≤3 cm and ulcer-positive lesions. The vital status at 5 years after ESD was confirmed in all (100%) patients. No local or metastatic recurrence was detected; however, 26 metachronous gastric cancers developed, and 1 patient died of metachronous gastric cancer. The 5-year disease-specific and overall survival rates were 99.5% (95% confidence interval [CI], 97.2%-100%) and 93.9% (95% CI, 89.8%-96.4%), respectively.
CONCLUSION CONCLUSIONS
ESD for EGC that fulfills the expanded criteria is feasible and shows favorable long-term outcomes.

Identifiants

pubmed: 32663347
doi: 10.1111/jgh.15182
pmc: PMC7983953
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

664-670

Informations de copyright

© 2020 The Authors. Journal of Gastroenterology and Hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

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Auteurs

Satoki Shichijo (S)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Noriya Uedo (N)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Takashi Kanesaka (T)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Takashi Ohta (T)

Division of Gastroenterology, Kansai Rosai Hospital, Amagasaki, Japan.

Kentaro Nakagawa (K)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Yusaku Shimamoto (Y)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Masayasu Ohmori (M)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Masamichi Arao (M)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Taro Iwatsubo (T)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Sho Suzuki (S)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Kenshi Matsuno (K)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Hiroyoshi Iwagami (H)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Shuntaro Inoue (S)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Noriko Matsuura (N)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Akira Maekawa (A)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Hiroko Nakahira (H)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Sachiko Yamamoto (S)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Yoji Takeuchi (Y)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Koji Higashino (K)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Ryu Ishihara (R)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.

Keisuke Fukui (K)

Center for Cancer Control and Statistics, Osaka International Cancer Institute, Osaka, Japan.
Department of Medical Statistics, Research & Development Center, Osaka Medical College, Osaka, Japan.

Yuri Ito (Y)

Center for Cancer Control and Statistics, Osaka International Cancer Institute, Osaka, Japan.
Department of Medical Statistics, Research & Development Center, Osaka Medical College, Osaka, Japan.

Hiroyuki Narahara (H)

Department of Gastroenterology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

Shingo Ishiguro (S)

Pathology, Pathology and Cytology Laboratories, Inc, Tokyo, Japan.

Hiroyasu Iishi (H)

Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan.
Department of Gastroenterology, Itami City Hospital, Itami, Japan.

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