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創勝集團 - 全整合型國際化生物制藥公司

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學術論文及會議壁報

Osemitamab三聯療法一線治療晚期胃或胃食管結合部腺癌的I/II期更新療效分析

05 Dec, 2025

Authors:

Dan Liu1 , Jifang Gong1, Zengqing Guo2, Jingdong Zhang2, Weijian Guo2, Meili Sun2, Nong Xu2, Diansheng Zhong2, Jiayi Li2, Ning Li2, Dan Cao2, Fuyou Zhao2, Chuan Qi3, Zhenzhong Xia3, Chunhua Qian3, Lijuan Zhang3, Jianming Wang3, Li Xu3, Caroline Germa3, Lin Shen1

1. Peking University Cancer Hospital. 2. Investigator. 3. Sponsor employee.

Background:

Osemitamab is a humanized monoclonal antibody with improved affinity to claudin 18.2 (CLDN18.2) and has been observed to upregulate PD-L1 expression on CLDN18.2-positive tumor cells.

In vivo anti-tumor activity of osemitamab + anti-PD-1/PD-L1 antibody + chemotherapy was significantly stronger than any of the doublet combinations, regardless of PD-L1 CPS levels, making the triplet of osemitamab, nivolumab and CAPOX an attractive combination.

Promising efficacy of osemitamab plus CAPOX and nivolumab as first-line treatment for gastric or gastroesophageal junction (G/GEJ) cancer has been observed and reported previously at ASCO 2025. Here we report the exploratory efficacy analysis based on CLDN18.2 and PD-L1 expressions

Conclusions:

The updated data indicate that the combination of TST001 plus nivolumab and CAPOX for first-line treatment of patients with G/GEJ cancer is safe and well tolerated.

The exploratory efficacy analysis indicates that encouraging benefit of osemitamab in combination with standard of care in patients with G/GEJ cancer and the potential treatment benefit of osemitamab is consistent regardless of PD-L1 expression.