LAUSR

Endoscopic submucosal dissection (ESD) has been widely used as a curative treatment for early gastric cancers (EGCs). ESD has historically high en bloc and curative resection rates for EGCs, regardless of their size and location. ESD is a minimal invasive procedure compared to surgical gastrectomy, and is an advantageous approach due to preservation of the entire stomach. Despite these advantages, there is a concerning rate of newly developed gastric cancers in the preserved stomach after ESD. Metachronous gastric cancer (MGC) is defined as a newly developed gastric cancer occurring at a previously uninvolved site 1 year or more after index ESD. In this issue of Gut and Liver, Kim et al. evaluated the clinical outcomes of MGC after ESD for EGCs between the re-ESD and surgery groups. During the mean follow-up period of 66 months, MGC occurred in 117 of 1,302 patients (9%) who had undergone ESD for EGCs; of patients with MGC, 90 underwent re-ESD and 22 underwent surgery. In multivariate analysis, a low body mass index, multiplicity of index cancers, diffuse or mixed-type Lauren classification, submucosal or deeper invasion, and upper stomach location were factors associated with surgery for MGC. Interestingly, the surgical group showed a significantly shorter overall survival rate than the re-ESD group. Risk factors associated with development of MGC include male sex, old age, current smoking, severe atrophy, intestinal metaplasia, persistent Helicobacter pylori infection, pepsinogen (PG) I/II ratio ≤3, differentiated-type histology, and multiple initial gastric cancers. Male sex, old age, and current smoking are also potential risk factors for gastric cancer in the general population. According to Correa’s hypothesis, intestinaltype gastric cancer may develop as chronic H. pylori infection evolves over time to chronic gastritis, atrophy, intestinal metaplasia and dysplasia. Because ESD is an organ-sparing treatment, gastric mucosa with histologic changes remains after ESD for EGCs. Therefore, risk factors for MGC are like to those for intestinal-type gastric cancer. Some studies suggest that H. pylori eradication may not always reduce the development of MGC after ESD, especially in cases of multiple initial gastric cancers; severe atrophy with intestinal metaplasia represents the “point of no return” at which the development of gastric cancer can no longer be prevented by H. pylori eradication alone. On the contrary, many studies suggest that persistent H. pylori infection is a risk factor for MGC, and a recent meta-analysis shows that H. pylori eradication can effectively reduce rates of MGC. Therefore, H. pylori eradication is strongly recommended for prevention of MGC after ESD for EGCs. Serum PG I/II ratio can also be used as a predictive indicator of the development of MGC after ESD, as it is a reliable marker in the diagnosis of more extensive atrophy. Because gastric atrophy progresses from the antrum to the lower body, MGC is usually located at the lower third of the stomach and appears as a small, differentiated-type intramucosal cancer <20 mm in size. Most patients with MGC already have marked atrophy and intestinal metaplasia in the background gastric mucosa. Because H. pylori eradication decreases inflammation caused by H. pylori infection, it can become even more difficult to detect early MGC and its margins. Therefore,