Clin Endosc > Volume 54(2); 2021 > Article
Bang: Long-Term Outcomes of Endoscopic Submucosal Dissection of Undifferentiated-Type Early Gastric Cancer
Endoscopic submucosal dissection (ESD) is the standard treatment for the subset of patients with early gastric cancer (EGC) satisfying prespecified criteria. The long-term prognosis following ESD for cases of EGC meeting the ESD criteria (achievement of curative resection) is comparable to that achieved with surgical resection [1]. However, this long-term prognosis comparison categorized by the histology according to the differentiation, especially for undifferentiated-type EGC, has not been well established.
In the context of histology, undifferentiated-type EGC generally refers to poorly-differentiated tubular adenocarcinoma, signet-ring cell carcinoma, or poorly cohesive carcinoma [2]. Although undifferentiated-type EGC is included among the expanded indications of ESD, the rate of curative resection remains low, reported previously as 61.4% in a meta-analysis and 36.4% in a nationwide cohort study in Korea [3,4]. This implies that an unmet need persists regarding the accurate prediction of curative resection in undifferentiated-type EGC (difficulty in adopting a precise ESD indication). Therefore, proper candidate selection prior to ESD is important.
Endoscopists predict the probability of curative resection using the size and shape of the lesion and whether ulcers are present or not. The most fundamental hypothesis is that endoscopic resection can be performed with curative intent for EGCs without lymph node metastasis. Therefore, indications of ESD were established using the combination of factors associated with a negligible lymph-node metastasis rate from the retrospective analysis of surgically resected specimens [2]. These indications are categorized as per the histology of EGC according to the differentiation, size, and morphologic conditions of the involved lesion. However, optical endoscopic determination of the factors stated above involves operator-dependent characteristics. In the study of a Korean multicenter registry of ESD for undifferentiated-type EGC, there was a discrepancy between pre-ESD indications and post-ESD criteria in 36.7% of all lesions [4]. The underestimation of the size was the most common reason for non-curative resection (71.4%), followed by the underestimation of the invasion depth (32%) and unpredictability of lymphovascular invasion (14.9%) [4]. Undifferentiated-type EGC has distinctive growth patterns relative to differentiated-type EGC [2,4]. Undifferentiated-type EGC is known to extend laterally along the proliferative zone in the intermediate layer of the mucosa (subepithelial spreading), and the development pattern from the intermediate layer could lead to non-exposure to the surface mucosa, limiting the precise measurement of the size of the lesion [3]. Subepithelial-spreading signet-ring cell carcinoma is more prevalent than the epithelial-spreading type in cases with background gastric mucosal atrophy or intestinal metaplasia. Furthermore, ESD of the poorly-differentiated adenocarcinoma presents a stronger association with submucosal invasion relative to that of signet-ring cell carcinoma [4]. Although adopting a precise indication is important, undifferentiated-type EGC itself is a risk factor for an out-of-indication rate, leading to non-curative resection, so more strict indications might be necessary for pursuing the ESD of undifferentiated-type EGC [5].
In this issue of Clinical Endoscopy, Huh et al. reported a comparative evaluation of the long-term outcomes of ESD and surgery for undifferentiated-type EGC [6]. There was no difference in the overall survival and procedure-related adverse events with the five Korean studies of 429 and 1,236 patients who underwent ESD and surgery, respectively. However, ESD showed a higher recurrence rate and lower complete resection rate compared to those of surgery. Although the overall survival was not different between patients who underwent ESD and surgery in this meta-analysis, this could change depending on how the ESD indication was applied in each enrolled study. Four studies (among the five studies included in the meta-analysis) included resected lesions based on the expanded indication and showed no significant difference in overall survival between ESD and surgery. However, there is difficulty in adopting a precise indication in the ESD of undifferentiated-type EGC. This means ESD is often performed on the basis of the beyond expanded indication which is mistaken for expanded indication. Therefore, there could be a selection bias in the results of this meta-analysis because patients with lesions for which the expanded indication was applied correctly (satisfying expanded criteria) were retrospectively enrolled in each study. If we could adopt a precise indication of ESD, the prognosis would be good. One of the methods to compensate this unmet need would be the application of strict indications (i.e., ESD for smaller lesions) because the underestimation of the size was the most common reason for non-curative resection in a previous study [4].
Although a prospective trial of ESD for undifferentiated-type EGC that satisfied the expanded criteria reported an excellent long-term survival rate [4,7,8], more cautious application or restriction of ESD indications has been recommended, especially regarding the size categorization [2]. Most recently published studies have also indicated that small intramucosal undifferentiated-type EGC measuring less than 1.0 cm or 1.5 cm without lymphovascular invasion should be considered for ESD [9,10].
The indications of ESD for undifferentiated-type EGC have not been approved by all endoscopists. Therefore, practice patterns adopting ESD indications for undifferentiated-type EGC vary depending on the institution. However, the results of previous studies commonly suggested that ESD for the lesions satisfying the expanded criteria has a good prognosis. Therefore, efforts to apply precise indications are important.

NOTES

Conflicts of Interest: Chang Seok Bang has been an Associate Editor member of Clinical Endoscopy; however, he was not involved in the peer reviewer selection, evaluation, or decision process of this article. The author has no potential conflicts of interest.
Funding
Funding for this research was provided by the Bio & Medical Technology Development Program of the National Research Foundation (NRF), the Korean government, Ministry of Science and ICT (MSIT) (grant number NRF2017M3A9E8033253), and the Korean College of Helicobacter and Upper Gastrointestinal Research Foundation Grant (2017-08).
Author Contributions
Writing-original draft: Chang Seok Bang
Writing-review&editing: CSB

REFERENCES

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