Preoperative H. pylori Eradication Therapy Facilitates Precise Delineation in Early Gastric Cancer with Current H. pylori Infection
Introduction: Early gastric cancer with current Helicobacter pylori infection (HpC-EGC) is common, but it is still unclear whether H. pylori eradication therapy (Hp-ET) or endoscopic submucosal dissection (ESD) should be performed first. We evaluated Hp-ETs short-term effects on horizontal boundary...
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Published in | Digestive diseases (Basel) Vol. 42; no. 1; pp. 1 - 11 |
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Main Authors | , , , , , , , , , , , , , , , , |
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Basel, Switzerland
01.01.2024
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Abstract | Introduction: Early gastric cancer with current Helicobacter pylori infection (HpC-EGC) is common, but it is still unclear whether H. pylori eradication therapy (Hp-ET) or endoscopic submucosal dissection (ESD) should be performed first. We evaluated Hp-ETs short-term effects on horizontal boundary delineations of HpC-EGC in ESD. Methods: Prospectively enrolled HpC-EGC patients were randomly assigned to eradication or control groups. Operation scopes of HpC-EGC lesions were delineated with marking dots at 5 mm out of the endoscopic demarcation line by an independent endoscopist, unaware of eradication status, before formal circumferential incision. As representatives, precise delineation rate, the shortest distance of all marking dots to the pathological demarcation line in all slices of one intact resected specimen (D min ), and negative marking dot specimen rate were examined. Results: Twenty-three HpC-EGC patients (25 lesions) were allocated to eradication group and 26 patients (27 lesions) were allocated to the control group with similar eradication success rates and all were differentiated type. With improving background mucosa inflammation after Hp-ET and similar gastritis-like epithelium rates, 10 lesions (40.0%) in the eradication group were of precise delineation compared to control group with 2 lesions (7.4%) (relative risk = 5.40, 95% CI 1.31–22.28). D min of eradication and control groups were 4.17 ± 2.52 mm and 2.67 ± 2.30 mm (p = 0.029), accompanied by 4 (14.8%) and none (0.0%) specimens that exhibited positive marking dots (p = 0.11), respectively. Conclusion: For HpC-EGC patients, administrating eradication medication before ESD is beneficial for the precise delineation of lesions and reducing the risk of positive horizontal resection margins. |
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AbstractList | Introduction: Early gastric cancer with current Helicobacter pylori infection (HpC-EGC) is common, but it is still unclear whether H. pylori eradication therapy (Hp-ET) or endoscopic submucosal dissection (ESD) should be performed first. We evaluated Hp-ETs short-term effects on horizontal boundary delineations of HpC-EGC in ESD. Methods: Prospectively enrolled HpC-EGC patients were randomly assigned to eradication or control groups. Operation scopes of HpC-EGC lesions were delineated with marking dots at 5 mm out of the endoscopic demarcation line by an independent endoscopist, unaware of eradication status, before formal circumferential incision. As representatives, precise delineation rate, the shortest distance of all marking dots to the pathological demarcation line in all slices of one intact resected specimen (D min ), and negative marking dot specimen rate were examined. Results: Twenty-three HpC-EGC patients (25 lesions) were allocated to eradication group and 26 patients (27 lesions) were allocated to the control group with similar eradication success rates and all were differentiated type. With improving background mucosa inflammation after Hp-ET and similar gastritis-like epithelium rates, 10 lesions (40.0%) in the eradication group were of precise delineation compared to control group with 2 lesions (7.4%) (relative risk = 5.40, 95% CI 1.31–22.28). D min of eradication and control groups were 4.17 ± 2.52 mm and 2.67 ± 2.30 mm (p = 0.029), accompanied by 4 (14.8%) and none (0.0%) specimens that exhibited positive marking dots (p = 0.11), respectively. Conclusion: For HpC-EGC patients, administrating eradication medication before ESD is beneficial for the precise delineation of lesions and reducing the risk of positive horizontal resection margins. Early gastric cancer with current Helicobacter pylori infection (HpC-EGC) is common, but it is still unclear whether H. pylori eradication therapy (Hp-ET) or endoscopic submucosal dissection (ESD) should be performed first. We evaluated Hp-ETs short-term effects on horizontal boundary delineations of HpC-EGC in ESD. Prospectively enrolled HpC-EGC patients were randomly assigned to eradication or control groups. Operation scopes of HpC-EGC lesions were delineated with marking dots at 5 mm out of the endoscopic demarcation line by an independent endoscopist, unaware of eradication status, before formal circumferential incision. As representatives, precise delineation rate, the shortest distance of all marking dots to the pathological demarcation line in all slices of one intact resected specimen (Dmin), and negative marking dot specimen rate were examined. Twenty-three HpC-EGC patients (25 lesions) were allocated to eradication group and 26 patients (27 lesions) were allocated to the control group with similar eradication success rates and all were differentiated type. With improving background mucosa inflammation after Hp-ET and similar gastritis-like epithelium rates, 10 lesions (40.0%) in the eradication group were of precise delineation compared to control group with 2 lesions (7.4%) (relative risk = 5.40, 95% CI 1.31-22.28). Dmin of eradication and control groups were 4.17 ± 2.52 mm and 2.67 ± 2.30 mm (p = 0.029), accompanied by 4 (14.8%) and none (0.0%) specimens that exhibited positive marking dots (p = 0.11), respectively. For HpC-EGC patients, administrating eradication medication before ESD is beneficial for the precise delineation of lesions and reducing the risk of positive horizontal resection margins. |
Author | Feng, Yunlu Yan, Xuemin Wu, Dongsheng Wang, Qiang Fang, Weigang Jiao, Yuhao Yang, Aiming Zhou, Weixun Xiong, Dingkun Zou, Long Xu, Tao Yan, Zhiyu Zhang, Shengyu Wu, Xi Lai, Yamin Jiang, Qingwei Guo, Tao |
Author_xml | – sequence: 1 givenname: Zhiyu surname: Yan fullname: Yan, Zhiyu – sequence: 2 givenname: Long surname: Zou fullname: Zou, Long – sequence: 3 givenname: Qiang surname: Wang fullname: Wang, Qiang – sequence: 4 givenname: Shengyu surname: Zhang fullname: Zhang, Shengyu – sequence: 5 givenname: Yuhao surname: Jiao fullname: Jiao, Yuhao – sequence: 6 givenname: Dingkun surname: Xiong fullname: Xiong, Dingkun – sequence: 7 givenname: Qingwei surname: Jiang fullname: Jiang, Qingwei – sequence: 8 givenname: Tao surname: Guo fullname: Guo, Tao – sequence: 9 givenname: Yunlu surname: Feng fullname: Feng, Yunlu – sequence: 10 givenname: Dongsheng surname: Wu fullname: Wu, Dongsheng email: *Xi Wu, wuxi@pumch.cn, Weixun Zhou, zweixun@163.com – sequence: 11 givenname: Yamin surname: Lai fullname: Lai, Yamin – sequence: 12 givenname: Xuemin surname: Yan fullname: Yan, Xuemin – sequence: 13 givenname: Tao surname: Xu fullname: Xu, Tao email: *Xi Wu, wuxi@pumch.cn, Weixun Zhou, zweixun@163.com – sequence: 14 givenname: Weigang surname: Fang fullname: Fang, Weigang – sequence: 15 givenname: Xi surname: Wu fullname: Wu, Xi email: *Xi Wu, wuxi@pumch.cn, Weixun Zhou, zweixun@163.com – sequence: 16 givenname: Weixun surname: Zhou fullname: Zhou, Weixun email: *Xi Wu, wuxi@pumch.cn, Weixun Zhou, zweixun@163.com – sequence: 17 givenname: Aiming surname: Yang fullname: Yang, Aiming |
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Copyright | 2023 The Author(s). Published by S. Karger AG, Basel 2023 The Author(s). Published by S. Karger AG, Basel. |
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Keywords | Endoscopic submucosal dissection Timing H. pylori eradication Current H. pylori infection Early gastric cancer |
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Horiguchi N, Tahara T, Yamada H, Yoshida D, Okubo M, Nagasaka M. In vivo diagnosis of early-stage gastric cancer found after Helicobacter pylori eradication using probe-based confocal laser endomicroscopy. Dig Endosc. 2018;30(2):219–27. Yao KS. The endoscopic diagnosis of early gastric cancer. Ann Gastroenterol. 2013;26(1):11–22. Kamada T, Hata J, Sugiu K, Kusunoki H, Ito M, Tanaka S. Clinical features of gastric cancer discovered after successful eradication of Helicobacter pylori: results from a 9-year prospective follow-up study in Japan. Aliment Pharmacol Ther. 2005;21(9):1121–6. |
References_xml | – reference: Jeon HK, Lee SJ, Kim GH, Park DY, Lee BE, Song GA. Endoscopic submucosal dissection for undifferentiated-type early gastric cancer: short- and long-term outcomes. Surg Endosc. 2018;32(4):1963–70. – reference: Asada-Hirayama I, Kodashima S, Sakaguchi Y, Ono S, Niimi K, Mochizuki S. Magnifying endoscopy with narrow-band imaging is more accurate for determination of horizontal extent of early gastric cancers than chromoendoscopy. Endosc Int Open. 2016;4(6):e690–8. – reference: Yao KS. The endoscopic diagnosis of early gastric cancer. Ann Gastroenterol. 2013;26(1):11–22. – reference: Mao T, Wang Y, Yin F, Zhao Q, Yang L, Ding X. Association of endoscopic features of gastric mucosa with Helicobacter pylori infection in Chinese patients. Gastroenterol Res Pract. 2016;2016:6539639. – reference: Chmiela M, Karwowska Z, Gonciarz W, Allushi B, Stączek P. Host pathogen interactions in Helicobacter pylori related gastric cancer. World J Gastroenterol. 2017;23(9):1521–40. – reference: Horiguchi N, Tahara T, Yamada H, Yoshida D, Okubo M, Nagasaka M. In vivo diagnosis of early-stage gastric cancer found after Helicobacter pylori eradication using probe-based confocal laser endomicroscopy. Dig Endosc. 2018;30(2):219–27. – reference: Suzuki H, Oda I, Abe S, Sekiguchi M, Mori G, Nonaka S. High rate of 5-year survival among patients with early gastric cancer undergoing curative endoscopic submucosal dissection. Gastric Cancer. 2016;19(1):198–205. – reference: Cheng XJ, Lin JC, Tu SP. Etiology and prevention of gastric cancer. Gastrointest Tumors. 2016;3(1):25–36. – reference: Horiuchi Y, Fujisaki J, Yamamoto N, Omae M, Ishiyama A, Yoshio T. Diagnostic accuracy of demarcation of undifferentiated-type early gastric cancer after Helicobacter pylori eradication. J Gastroenterol. 2017;52(9):1023–30. – reference: Japanese Gastric Cancer Association. Japanese classification of gastric carcinoma: 3rd English edition. Gastric Cancer. 2011;14(2):101–12. – reference: Ito M, Tanaka S, Chayama K. Characteristics and early diagnosis of gastric cancer discovered after Helicobacter pylori eradication. Gut Liver. 2021;15(3):338–45. – reference: Chinese Society of Gastroenterology. Chinese study group on Helicobacter Pylori and peptic ulcer. Fifth Chinese national consensus report on the management of Helicobacter pylori infection. Chin J Dig. 2017;37(6):364–78. – reference: Japanese Gastric Cancer Association. Japanese gastric cancer treatment guidelines 2018 (5th edition). Gastric Cancer. 2021;24(1):1–21. – reference: Weng CY, Xu JL, Sun SP, Wang KJ, Lv B. Helicobacter pylori eradication: exploring its impacts on the gastric mucosa. World J Gastroenterol. 2021;27(31):5152–70. – reference: Kato M, Terao S, Adachi K, Nakajima S, Ando T, Yoshida N. Changes in endoscopic findings of gastritis after cure of H. pylori infection: multicenter prospective trial. Dig Endosc. 2013;25(3):264–73. – reference: Kim GH, Jung HY. Endoscopic resection of gastric cancer. Gastrointest Endosc Clin N Am. 2021;31(3):563–79. – reference: Toyonaga T, Nishino E, Hirooka T, Ueda C, Noda K. Intraoperative bleeding in endoscopic submucosal dissection in the stomach and strategy for prevention and treatment. Dig Endosc. 200618s1s1237. – reference: Saka A, Yagi K, Nimura S. Endoscopic and histological features of gastric cancers after successful Helicobacter pylori eradication therapy. Gastric Cancer. 2016;19(2):524–30. – reference: Ito M, Tanaka S, Takata S, Oka S, Imagawa S, Ueda H. Morphological changes in human gastric tumours after eradication therapy of Helicobacter pylori in a short-term follow-up. Aliment Pharmacol Ther. 2005;21(5):559–66. – reference: Yakirevich E, Resnick MB. Pathology of gastric cancer and its precursor lesions. Gastroenterol Clin North Am. 2013;42(2):261–84. – reference: Shichijo S, Hirata Y. Characteristics and predictors of gastric cancer after Helicobacter pylori eradication. World J Gastroenterol. 2018;24(20):2163–72. – reference: Kwak HW, Choi IJ, Cho SJ, Lee JY, Kim CG, Kook MC. Characteristics of gastric cancer according to Helicobacter pylori infection status. J Gastroenterol Hepatol. 2014;29(9):1671–7. – reference: Kamada T, Hata J, Sugiu K, Kusunoki H, Ito M, Tanaka S. Clinical features of gastric cancer discovered after successful eradication of Helicobacter pylori: results from a 9-year prospective follow-up study in Japan. Aliment Pharmacol Ther. 2005;21(9):1121–6. – reference: Saragoni L, Scarpi E, Ravaioli A, Morgagni P, Roviello F, Vindigni C. Early gastric cancer: clinical behavior and treatment options. Results of an Italian multicenter study on behalf of the Italian gastric cancer research group (GIRCG). Oncologist. 2018;23(7):852–8. – reference: Choi IJ, Kook MC, Kim YI, Cho SJ, Lee JY, Kim CG. Helicobacter pylori therapy for the prevention of metachronous gastric cancer. N Engl J Med. 2018;378(12):1085–95. – reference: Yao K, Anagnostopoulos GK, Ragunath K. Magnifying endoscopy for diagnosing and delineating early gastric cancer. Endoscopy. 2009;41(5):462–7. – reference: Fichman S, Niv Y. Histological changes in the gastric mucosa after Helicobacter pylori eradication. Eur J Gastroenterol Hepatol. 2004;16(11):1183–8. – reference: Xu SS, Chai NL, Tang XW, Linghu EQ, Wang SS, Li B. Characteristics of metachronous gastric neoplasms after curative endoscopic submucosal dissection for early gastric neoplasms. Chin Med J. 2021;134(21):2603–10. – reference: Huang RJ, Sharp N, Talamoa RO, Ji HP, Hwang JH, Palaniappan LP. One size does not fit all: marked heterogeneity in incidence of and survival from gastric cancer among Asian American subgroups. Cancer Epidemiol Biomarkers Prev. 2020;29(5):903–9. – reference: Park CH, Yang DH, Kim JW, Kim JH, Kim JH, Min YW. Clinical practice guideline for endoscopic resection of early gastrointestinal cancer. Clin Endosc. 2020;53(2):142–66. – reference: Akahoshi K, Motomura Y, Kubokawa M, Gibo J, Kinoshita N, Osada S. Endoscopic submucosal dissection for early gastric cancer using the clutch cutter: a large single-center experience. Endosc Int Open. 2015;3(5):e432–8. – reference: Kim SG. Endoscopic resection of early gastric cancer. In: Oliviu P, Marcel T, editors. Therapeutic gastrointestinal endoscopyLondonIntechOpen. 2011. p. 1324. – reference: Ono H, Yao K, Fujishiro M, Oda I, Nimura S, Yahagi N. Guidelines for endoscopic submucosal dissection and endoscopic mucosal resection for early gastric cancer. Dig Endosc. 2016;28(1):3–15. – reference: Kobayashi M, Hashimoto S, Nishikura K, Mizuno K, Takeuchi M, Sato Y. Magnifying narrow-band imaging of surface maturation in early differentiated-type gastric cancers after Helicobacter pylori eradication. 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Snippet | Introduction: Early gastric cancer with current Helicobacter pylori infection (HpC-EGC) is common, but it is still unclear whether H. pylori eradication... Early gastric cancer with current Helicobacter pylori infection (HpC-EGC) is common, but it is still unclear whether H. pylori eradication therapy (Hp-ET) or... |
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SubjectTerms | Stomach and Duodenum: Research Article |
Title | Preoperative H. pylori Eradication Therapy Facilitates Precise Delineation in Early Gastric Cancer with Current H. pylori Infection |
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