Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer

Abstract Claudin 18.2 has emerged as a promising therapeutic target in gastric cancer based on phase 3 studies. However, clinicopathologic features associated with claudin 18.2 overexpression have not been comprehensively studied specifically for patients with resectable gastric cancer. This retrosp...

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Main Authors: Hyung-Don Kim, Eugene Choi, Jinho Shin, In-Seob Lee, Chang Seok Ko, Min-Hee Ryu, Young Soo Park
Format: Article
Language:English
Published: Nature Portfolio 2023-11-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-47178-6
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author Hyung-Don Kim
Eugene Choi
Jinho Shin
In-Seob Lee
Chang Seok Ko
Min-Hee Ryu
Young Soo Park
author_facet Hyung-Don Kim
Eugene Choi
Jinho Shin
In-Seob Lee
Chang Seok Ko
Min-Hee Ryu
Young Soo Park
author_sort Hyung-Don Kim
collection DOAJ
description Abstract Claudin 18.2 has emerged as a promising therapeutic target in gastric cancer based on phase 3 studies. However, clinicopathologic features associated with claudin 18.2 overexpression have not been comprehensively studied specifically for patients with resectable gastric cancer. This retrospective study included 299 patients with stage I–III resectable gastric cancer who underwent curative surgical resection. Possible associations between claudin 18.2 overexpression (moderate-to-strong expression in ≥ 75% by the 43-14A clone) and clinicopathologic features and survival outcomes were analyzed. There were 90 (30.1%), 96 (32.1%), and 113 (37.8%) patients with stage I, II, and III disease, respectively. Claudin 18.2 overexpression was noted in 139 out of 299 patients (46.5%). Claudin 18.2 overexpression was associated with a younger age, a lower invasion depth limited to the mucosa/submucosa, and less frequent lymphovascular invasion. Claudin 18.2 overexpression was also associated with Borrmann type 4 among patients with advanced gastric cancer and the diffuse histological type. Claudin 18.2 overexpression was not an independent factor for survival outcomes. In conclusion, claudin 18.2 was overexpressed in almost half of resectable gastric cancer patients. Claudin 18.2 overexpression was associated with some clinicopathological characteristics, but was not an independent prognostic factor in a localized setting.
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spelling doaj.art-7eddc8c5e5ef4bc8a57e943680a96f8b2023-11-19T13:08:46ZengNature PortfolioScientific Reports2045-23222023-11-011311810.1038/s41598-023-47178-6Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancerHyung-Don Kim0Eugene Choi1Jinho Shin2In-Seob Lee3Chang Seok Ko4Min-Hee Ryu5Young Soo Park6Department of Oncology, Asan Medical Center, University of Ulsan College of MedicineDepartment of Pathology, Asan Medical Center, University of Ulsan College of MedicineDepartment of Pathology, Asan Medical Center, University of Ulsan College of MedicineDepartment of Surgery, Asan Medical Center, University of Ulsan College of MedicineDepartment of Surgery, Asan Medical Center, University of Ulsan College of MedicineDepartment of Oncology, Asan Medical Center, University of Ulsan College of MedicineDepartment of Pathology, Asan Medical Center, University of Ulsan College of MedicineAbstract Claudin 18.2 has emerged as a promising therapeutic target in gastric cancer based on phase 3 studies. However, clinicopathologic features associated with claudin 18.2 overexpression have not been comprehensively studied specifically for patients with resectable gastric cancer. This retrospective study included 299 patients with stage I–III resectable gastric cancer who underwent curative surgical resection. Possible associations between claudin 18.2 overexpression (moderate-to-strong expression in ≥ 75% by the 43-14A clone) and clinicopathologic features and survival outcomes were analyzed. There were 90 (30.1%), 96 (32.1%), and 113 (37.8%) patients with stage I, II, and III disease, respectively. Claudin 18.2 overexpression was noted in 139 out of 299 patients (46.5%). Claudin 18.2 overexpression was associated with a younger age, a lower invasion depth limited to the mucosa/submucosa, and less frequent lymphovascular invasion. Claudin 18.2 overexpression was also associated with Borrmann type 4 among patients with advanced gastric cancer and the diffuse histological type. Claudin 18.2 overexpression was not an independent factor for survival outcomes. In conclusion, claudin 18.2 was overexpressed in almost half of resectable gastric cancer patients. Claudin 18.2 overexpression was associated with some clinicopathological characteristics, but was not an independent prognostic factor in a localized setting.https://doi.org/10.1038/s41598-023-47178-6
spellingShingle Hyung-Don Kim
Eugene Choi
Jinho Shin
In-Seob Lee
Chang Seok Ko
Min-Hee Ryu
Young Soo Park
Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer
Scientific Reports
title Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer
title_full Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer
title_fullStr Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer
title_full_unstemmed Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer
title_short Clinicopathologic features and prognostic value of claudin 18.2 overexpression in patients with resectable gastric cancer
title_sort clinicopathologic features and prognostic value of claudin 18 2 overexpression in patients with resectable gastric cancer
url https://doi.org/10.1038/s41598-023-47178-6
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