This clinical trial focuses on patients with T-cell acute lymphoblastic leukemia and T-cell acute lymphoblastic lymphoma, which are types of blood cancers. The study involves a treatment called OC-1, which uses a special type of cell therapy. In this treatment, a patient’s own T-cells, a type of white blood cell, are modified outside the body using a lentiviral vector. This vector helps the T-cells develop a chimeric antigen receptor (CAR) that specifically targets a protein called CD1a on cancer cells. The modified T-cells, known as hCD1a-CAR T cells, are then infused back into the patient’s bloodstream.
The purpose of this study is to monitor patients who have already received the OC-1 cell therapy. The study will follow these patients for up to 15 years to check for any delayed side effects or adverse events. This long-term follow-up is important to ensure the safety of the treatment and to understand any potential risks that may arise over time. The study will look at various outcomes, such as the number of serious side effects, the development of new health issues, and the overall survival of patients after receiving the therapy.
During the study, researchers will also assess how long the OC-1 cells remain in the body and how they affect the patient’s health. This includes checking for the presence of the modified T-cells in the blood and evaluating their impact on the patient’s immune system. The study aims to provide valuable information about the long-term effects of this innovative treatment for patients with these challenging types of cancer.



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