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Publication Name World Journal of Gastroenterology
Manuscript ID 122906
Country China
Category Gastroenterology & Hepatology
Manuscript Type Minireviews
Article Title Research advances in targeting claudin 18.2 in pancreatic ductal adenocarcinoma treatment
Manuscript Source Unsolicited Manuscript
All Author List Yu-Han Wei, Shun-Chao Zhang, Bing-Jie Guan, Jia-Ning Jian, Chun-Guang Li, Ze-Kun Wang, Hao-Ran Qu, Zhi-Gang Li, Meng-Ya Liu and Jun-Tao Wang
Funding Agency and Grant Number
Funding Agency Grant Number
TCM Scientific Research Special Project of Henan Province No. 2024ZY2100
TCM Scientific Research Special Project of Henan Province No. 2022ZY2046
Henan Province Traditional Chinese Medicine Special Program Collaborative Project No. 2025 LHZX3001
National Construction Project for TCM Master’s Heritage Workshop, Letter[2022] No. 245
Henan Province Collaborative Innovation Center of Prevention and Treatment of Major Diseases by Chinese and Western Medicine, Letter[2023] No. 413
National Cultivation Centers for Priority Specialties of TCM, Letter[2024] No. 90
Henan TCM Qingmiao Young Talents Cultivation Program, Letter[2024] No. 4
Zhongjing Three Distinguished Talents Project Zhongjing Young Distinguished Physician, Document[2025] No. 116
Corresponding Author Jun-Tao Wang, MD, Department of Oncology, Ward 2, The Third Affiliated Hospital of Henan University of Chinese Medicine, No. 63 Dongming Road, Zhengzhou 450008, Henan Province, China. wjuntao@yeah.net
Key Words Claudin 18.2; Pancreatic ductal adenocarcinoma; Targeted therapy; Research progress; Treatment
Core Tip Claudin 18.2 (CLDN18.2) is expressed in pancreatic ductal adenocarcinoma (PDAC) and represents a promising therapeutic target. This review summarizes current evidence on CLDN18.2-directed therapies, including monoclonal antibodies, antibody drug conjugates, chimeric antigen receptor-T cells, bispecific antibodies, and other emerging strategies. We also outline unique challenges specific to CLDN18.2-positive PDAC, such as an abundance of cancer-associated fibroblasts, a profoundly immunosuppressive microenvironment, and intratumoral antigen heterogeneity. At present, this field remains in its preliminary stage, with most available data derived from small-scale clinical studies or extrapolated from gastric cancer research. Further PDAC-tailored preclinical and clinical investigations are urgently needed.
Citation Wei YH, Zhang SC, Guan BJ, Jian JN, Li CG, Wang ZK, Qu HR, Li ZG, Liu MY, Wang JT. Research advances in targeting claudin 18.2 in pancreatic ductal adenocarcinoma treatment. World J Gastroenterol 2026; In press
Received
2026-05-06 07:29
Peer-Review Started
2026-05-06 07:29
First Decision by Editorial Office Director
Return for Revision
2026-07-06 02:57
Revised
2026-07-18 09:10
Publication Fee Transferred
2026-07-24 04:11
Second Decision by Editor
2026-08-26 02:52
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2026-08-26 08:37
Articles in Press
2026-08-26 08:37
Edit the Manuscript by Language Editor
Typeset the Manuscript
ISSN 1007-9327 (print) and 2219-2840 (online)
Open Access This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See Permissions. Published by Baishideng Publishing Group Inc.
Copyright ©Author(s) (or their employer(s)) 2026. No commercial re-use. See Permissions. Published by Baishideng Publishing Group Inc.
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