Endoscopic features associated with development of metachronous gastric cancer in patients who underwent endoscopic resection followed by Helicobacter pylori eradication

Background and Aim The preventive effect of Helicobacter pylori (HP) eradication on metachronous gastric cancer development after endoscopic resection remains controversial. The aim of the present study was to identify specific endoscopic features that correlated with the risk of metachronous gastri...

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Veröffentlicht in:Digestive endoscopy 2016-05, Vol.28 (4), p.434-442
Hauptverfasser: Moribata, Kosaku, Kato, Jun, Iguchi, Mikitaka, Nakachi, Kenichiro, Maeda, Yoshimasa, Shingaki, Naoki, Niwa, Toru, Deguchi, Hisanobu, Inoue, Izumi, Maekita, Takao, Tamai, Hideyuki, Ichinose, Masao
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Sprache:eng
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Zusammenfassung:Background and Aim The preventive effect of Helicobacter pylori (HP) eradication on metachronous gastric cancer development after endoscopic resection remains controversial. The aim of the present study was to identify specific endoscopic features that correlated with the risk of metachronous gastric cancer development after endoscopic submucosal dissection (ESD) using both endoscopic findings before ESD and changes of findings after HP eradication. Methods This retrospective study investigated 122 consecutive patients who underwent ESD for early gastric cancer and successful HP eradication after ESD. Endoscopic findings linked with HP before ESD and changes after HP eradication were evaluated according to the development of metachronous cancer. Results Most patients showed severe atrophy and intestinal metaplasia (IM) before ESD (97% and 83%, respectively). Improvement of spotty redness, improvement of diffuse redness, emergence of patchy redness, and emergence of map‐like redness were frequent findings after HP eradication (52%, 50%, 54%, and 32%, respectively). Kaplan–Meier curves indicated that patients without IM before ESD never developed metachronous cancer, whereas patients with emergence of map‐like redness after HP eradication were significantly more likely to develop metachronous cancer (log–rank test, P = 0.031 and P 
ISSN:0915-5635
1443-1661
DOI:10.1111/den.12581