Metastatic gastric cancer target lesion complete response with Claudin18.2-CAR T cells.

Journal: Journal For Immunotherapy Of Cancer
Published:
Abstract

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. Clinical Insight: Claudin18.2-targeted CAR T cells can safely provide complete objective and ctDNA response in salvage metastatic GC.

Authors
Gregory Botta, Joseph Chao, Hong Ma, Michael Hahn, Gloria Sierra, Jie Jia, Amanda Hendrix, Joy Nolte Fong, Audrey Ween, Peter Vu, Aaron Miller, Michael Choi, Benjamin Heyman, Gregory Daniels, Dan Kaufman, Catriona Jamieson, Zonghai Li, Ezra Cohen
Relevant Conditions

Stomach Cancer, Leukemia