SmarT cell combined with PD-1 blockade and SOX as first-line treatment for patients with advanced gastric/gastroesophageal junction adenocarcinoma.

Q Qin Liu J Jia Wei (State Key Laboratory of Microbial Technology, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University) L Lianru Zhang (Department of Oncology, Nanjing Drum Tower Hospital & Group's Suqian Hospital, Medical School of Nanjing University, Suqian, China) Y Yang Yang J Jie Shao K Kun Lu (Zhejiang Key Laboratory of Intelligent Manufacturing for Functional Chemicals, College of Chemical and Biological Engineering) J Jiaqi Xie (College of Smart Materials and Future Energy, and State Key Laboratory of Photovoltaic Science and Technology Fudan University Shanghai 200438 China) J Ju Yang B Baorui Liu

Abstract

e16082 Background: Although PD-1 blokade plus chemotherapy has achieved a preferable response rate for advanced advanced gastric/gastroesophageal junction adenocarcinoma (GC/GEJC), patient survival remains unsatisfactory. In this study, we evaluated the efficacy and safety of a combination treatment of SmarT cell combined with PD-1 blockade and SOX in patients with advanced GC/GEJC. Methods: In this study, we enrolled adults (≥18 years) with previously untreated, unresectable, non-HER2-positive GC/GEJC, regardless of PD-ligand 1 (PD-L1) expression. Patients were assigned to PD-1 mAb plus chemotherapy (Tegafur and oxaliplatin every 3 weeks), or PD-1 mAb plus chemotherapy. Results: The Overall response rates were 66% (33/50) and 52% (26/50) for SmarT cell plus PD-1 mAb as well as chemotherapy and PD-1 mAb plus chemotherapy. The disease controlled rates for both groups were 94% and 80.0%, respectively. The median follow-up for PFS was 207 days for PD-1 mAb plus chemotherapy. While the median PFS for SmarT group has not been reached. The most common any-grade treatment-related adverse events were nausea, elevated liver enzymes, and peripheral leukemia reduction across both groups. No new safety signals were identified. Conclusions: SmarT cell shows superior ORR along with PFS benefit and an acceptable safety profile, in combination with PD-1 mAb plus chemotherapy versus PD-1 mAb plus chemotherapy in previously untreated patients with advanced gastric or gastroesophageal junction adenocarcinoma. Clinical trial information: ChiCTR2200061306 .

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (9)

Q

Qin Liu

J

Jia Wei

State Key Laboratory of Microbial Technology, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University

L

Lianru Zhang

Department of Oncology, Nanjing Drum Tower Hospital & Group's Suqian Hospital, Medical School of Nanjing University, Suqian, China

Y

Yang Yang

J

Jie Shao

K

Kun Lu

Zhejiang Key Laboratory of Intelligent Manufacturing for Functional Chemicals, College of Chemical and Biological Engineering

J

Jiaqi Xie

College of Smart Materials and Future Energy, and State Key Laboratory of Photovoltaic Science and Technology Fudan University Shanghai 200438 China

J

Ju Yang

B

Baorui Liu