医学
嵌合抗原受体
免疫疗法
癌症研究
淋巴瘤
癌症
T细胞
肿瘤科
内科学
免疫学
免疫系统
作者
Gregory P. Botta,Joseph Chao,H. Ma,Michael G. Hahn,Gloria Sierra,Jie Jia,Amanda Y Hendrix,Joy Nolte Fong,Audrey Ween,Peter Vu,Aaron Miller,Michael Y. Choi,Benjamin Heyman,Gregory A. Daniels,Dan S. Kaufman,Catriona Jamieson,Zonghai Li,Ezra E.W. Cohen
标识
DOI:10.1136/jitc-2023-007927
摘要
Treatment of hematologic malignancies with patient-derived anti-CD19 chimeric antigen receptor (CAR) T-cells has demonstrated long-term remissions for patients with otherwise treatment-refractory advanced leukemia and lymphoma. Conversely, CAR T-cell treatment of solid tumors, including advanced gastric cancer (GC), has proven more challenging due to on-target off-tumor toxicities, poor tumor T-cell infiltration, inefficient CAR T-cell expansion, immunosuppressive tumor microenvironments, and demanding preconditioning regimens. We report the exceptional results of autologous Claudin18.2-targeted CAR T cells (CT041) in a patient with metastatic GC, who had progressed on four lines of combined systemic chemotherapy and immunotherapy. After two CT041 infusions, the patient had target lesion complete response and sustained an 8-month overall partial response with only minimal ascites. Moreover, tumor-informed circulating tumor DNA (ctDNA) reductions coincided with rapid CAR T-cell expansion and radiologic response. No severe toxicities occurred, and the patient's quality of life significantly improved. This experience supports targeting Claudin18.2-positive GC with CAR T-cell therapy and helps to validate ctDNA as a biomarker in CAR T-cell therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI