Comparison of Prognosis and Metachronous Gastric Tumor Rates After Endoscopic Submucosal Dissection Between Gastric Neoplasm of Fundic Gland Type Neoplasms and Conventional Gastric Adenocarcinoma

被引:0
作者
Hayasaka, Junnosuke [1 ]
Hoteya, Shu [1 ]
Suzuki, Yugo [1 ]
Ochiai, Yorinari [1 ]
Mitsunaga, Yutaka [1 ]
Odagiri, Hiroyuki [1 ]
Masui, Akira [1 ]
Kikuchi, Daisuke [1 ]
Takazawa, Yutaka [2 ]
机构
[1] Toranomon Gen Hosp, Gastroenterol, Tokyo, Japan
[2] Toranomon Gen Hosp, Pathol, Tokyo, Japan
关键词
metachronous tumor; prognosis; oxyntic gland adenoma; gafg; fundic gland type; PROPOSAL; CANCER;
D O I
10.7759/cureus.58467
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Gastric neoplasm of the fundic gland type (GNFG) is a tumor with a good prognosis. However, since it has not been compared with conventional gastric adenocarcinoma (CGA), it is unknown whether it has a good prognosis or requires surveillance after treatment. The purpose of this study was to determine the prognosis and metachronous gastric tumor rates compared with those of CGA. Methods: We conducted a single -center, retrospective, matched-cohort study using our database from January 2010 to December 2021. We extracted GNFG data from the endoscopic submucosal dissection (ESD) database and matched patients with conventional early gastric cancer as controls in a 1:4 ratio by age and sex. GNFG and CGA were compared for the overall survival (OS), disease-specific survival, progression -free survival, and metachronous gastric tumor rates. Results: Overall, 43 lesions were GNFG and 164 CGAs were matched. There were three deaths in the GNFG group and 11 deaths in the CGA group. There was no significant difference in the OS between the two groups (P=0.81). The five -year OS rates for the GNFG and CGA groups were 90.9% and 92.9%, respectively. No disease-specific deaths or recurrences were observed in either group. There was no significant difference in the cumulative metachronous gastric tumor rate between the two groups (P=0.17). The cumulative fiveyear metachronous gastric tumor rates for the GNFG and CGA groups were 6.6% and 2.5%, respectively. Conclusions: The prognosis for GNFG is good, however, not better than that for CGA. The metachronous gastric tumor rate after ESD in GNFG was not lower than that in CGA. Therefore, after ESD, GNFG may need to be managed in the same way as CGA.
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