Abstract 1534: OriC613: A novel therapeutic strategy for gastric and pancreatic cancers utilizing dual-targeting CAR-T cells against MSLN and CLDN18.2 with a favorable safety profile and potent efficacy

Abstract Background: CAR-T cell therapy has demonstrated significant efficacy in hematologic malignancies; however, its application to solid tumors remains limited by on-target, off-tumor toxicity. Mesothelin(MSLN) and claudin 18.2(CLDN18.2) are tumor-associated antigens overexpressed in several solid tumors with minimal co-expression in normal tissues, which presents a therapeutic opportunity for a dual-targeting strategy to enhance tumor selectivity. Methods: To address gastric toxicity observed with CLDN18.2-directed CAR-T cells in preclinical models, we developed OriC613, a dual-antigen targeting CAR-T based on AND-logic gate. The construct incorporates a high-affinity anti-CLDN18.2 scFv and a moderate-affinity anti-MSLN VHH, engineered to achieve full T-cell activation only upon engagement of both antigens. Results: OriC613 demonstrated a favorable safety profile characterized by the absence of cytotoxic activity against CLDN18.2-positive normal gastric models. It exhibited enhanced cytotoxic potency against dual-positive tumor compared to conventional MSLN-targeted CAR-T. In pancreatic cancer re-challenge models, it promoted continued T-cell expansion and maintained cytokine production capacity. OriC613 mediated significant tumor regression in high-burden gastric in-vivo model, demonstrating robust antitumor activity while maintaining the safety profile. It also supported sustained T-cell persistence with detectable engraftment in bone marrow and spleen. Conclusions: OriC613 demonstrates potent antitumor activity and reduced toxicity profile by leveraging co-expression of MSLN and CLDN18.2. These preclinical findings support further clinical development of this dual-targeting CAR-T approach in patients with gastric or pancreatic adenocarcinoma. Citation Format: Xiaowen He, Shasha Yang, Hao Guo, Huajing Wang, Xuefeng Kong, Zhongjun Shi, . OriC613: A novel therapeutic strategy for gastric and pancreatic cancers utilizing dual-targeting CAR-T cells against MSLN and CLDN18.2 with a favorable safety profile and potent efficacy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1534.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-1534
Primary Topic
CAR-T cell therapy research
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article
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article

Abstract 1534: OriC613: A novel therapeutic strategy for gastric and pancreatic cancers utilizing dual-targeting CAR-T cells against MSLN and CLDN18.2 with a favorable safety profile and potent efficacy

Xuefeng Kong, X. He, Zhongjun Shi, Huajing Wang et al.
Cancer Research
CAR-T cell therapy research
article

Abstract 1534: OriC613: A novel therapeutic strategy for gastric and pancreatic cancers utilizing dual-targeting CAR-T cells against MSLN and CLDN18.2 with a favorable safety profile and potent efficacy

Xuefeng Kong, X. He, Zhongjun Shi, Huajing Wang, Hao Guo, Shasha Yang
article en

Abstract

Abstract Background: CAR-T cell therapy has demonstrated significant efficacy in hematologic malignancies; however, its application to solid tumors remains limited by on-target, off-tumor toxicity. Mesothelin(MSLN) and claudin 18.2(CLDN18.2) are tumor-associated antigens overexpressed in several solid tumors with minimal co-expression in normal tissues, which presents a therapeutic opportunity for a dual-targeting strategy to enhance tumor selectivity. Methods: To address gastric toxicity observed with CLDN18.2-directed CAR-T cells in preclinical models, we developed OriC613, a dual-antigen targeting CAR-T based on AND-logic gate. The construct incorporates a high-affinity anti-CLDN18.2 scFv and a moderate-affinity anti-MSLN VHH, engineered to achieve full T-cell activation only upon engagement of both antigens. Results: OriC613 demonstrated a favorable safety profile characterized by the absence of cytotoxic activity against CLDN18.2-positive normal gastric models. It exhibited enhanced cytotoxic potency against dual-positive tumor compared to conventional MSLN-targeted CAR-T. In pancreatic cancer re-challenge models, it promoted continued T-cell expansion and maintained cytokine production capacity. OriC613 mediated significant tumor regression in high-burden gastric in-vivo model, demonstrating robust antitumor activity while maintaining the safety profile. It also supported sustained T-cell persistence with detectable engraftment in bone marrow and spleen. Conclusions: OriC613 demonstrates potent antitumor activity and reduced toxicity profile by leveraging co-expression of MSLN and CLDN18.2. These preclinical findings support further clinical development of this dual-targeting CAR-T approach in patients with gastric or pancreatic adenocarcinoma. Citation Format: Xiaowen He, Shasha Yang, Hao Guo, Huajing Wang, Xuefeng Kong, Zhongjun Shi, . OriC613: A novel therapeutic strategy for gastric and pancreatic cancers utilizing dual-targeting CAR-T cells against MSLN and CLDN18.2 with a favorable safety profile and potent efficacy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 1534.

Cancer ResearchVol. 86(7_Supplement)
Regend Therapeutics (China) (CN)
Good health and well-being
Openalex Percentile: Top 8%
CAR-T cell therapy research
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