AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (1.8 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Review | Open Access

A New Paradigm of Bispecific Antibodies in Clinical Management of Gastrointestinal Cancers

Huimin Zhao#,1Xiuran Wang#,2Zhimeng Fan3Ai Sun4Changhua Zhang1( )Chunhui Sun1( )
Digestive Diseases Center, Research Center, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, China
College of Laboratory Animal Science, Shandong First Medical University, Jinan, China
Division of Oncology, Department of Clinical Sciences, Lund University, Lund, Sweden
Breeding and Biotechnology Research Laboratory, Beijing Academy of Agriculture and Forestry Sciences, Beijing, China

#These authors contributed equally to this work

Show Author Information

Abstract

Gastrointestinal (GI) cancers represent a significant global health burden, characterized by high incidence, poor prognosis, and limited response to monotherapies. The advent of bispecific antibodies (BsAbs) has introduced a novel therapeutic paradigm, enabling dual targeting of tumor-associated antigens and immune effectors to enhance antitumor immunity. This review provides a comprehensive overview of recent advances in bsAb-based immunotherapy across major GI malignancies, including colorectal, gastric, pancreatic, biliary tract, esophageal, and liver cancers. We summarize key molecular targets and highlight representative clinical candidates such as CEA-TCB and RG7802. The discussion extends to innovative strategies involving BsAbs in modulating the immunosuppressive tumor microenvironment and overcoming resistance mechanisms. Furthermore, we explore promising combination therapies involving BsAbs with chemotherapy and immune checkpoint inhibitors (ICIs). The role of artificial intelligence in target prediction and structure optimization is also examined, alongside the potential of personalized immune strategies. Despite promising therapeutic potential, BsAbs face challenges including cytokine release syndrome (CRS), on-target/off-tumor toxicity, tumor heterogeneity-driven resistance, and tumor microenvironment (TME). Current strategies to improve therapeutic index encompass affinity-tuned designs, conditional activation mechanisms, biomarker-driven patient stratification, combination therapies, and artificial intelligence (AI)-guided optimization, warranting continued interdisciplinary research efforts. We conclude by outlining future research directions and emphasizing the importance of interdisciplinary, multicenter collaborations to accelerate clinical translation and maximize the therapeutic potential of BsAbs in GI oncology. In summary, the aim of this study is to critically evaluate the current landscape of BsAb-based immunotherapy in gastrointestinal cancers, synthesizing emerging molecular targets, evaluating clinical trial outcomes, identifying key challenges limiting therapeutic efficacy, and proposing evidence-based strategies to optimize future BsAb development.

References

【1】
【1】
 
 
Oncology Research
Article number: 7

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Zhao H, Wang X, Fan Z, et al. A New Paradigm of Bispecific Antibodies in Clinical Management of Gastrointestinal Cancers. Oncology Research, 2026, 34(7): 7. https://doi.org/10.32604/or.2026.078825

30

Views

0

Downloads

0

Crossref

0

Web of Science

0

Scopus

Received: 08 January 2026
Accepted: 25 March 2026
Published: 16 June 2026
© The Author 2026.

This work is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.