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Korean Journal of Medicine ; : 152-158, 2019.
Article in Korean | WPRIM | ID: wpr-759927

ABSTRACT

CD19 chimeric antigen receptor T-cell (CAR-T) therapy, a genetically engineered cell therapy, showed unprecedented efficacy in the treatment of relapsed or refractory diffuse large B-cell lymphoma. Two agents, axicabtagene ciloleucel and tisagenlecleucel, were approved by the Food and Drug Administration in 2017. However, CAR-T therapy is a treatment with complex logistics and high costs, as well as inherent adverse events, including cytokine-release syndrome and neurotoxicity. In addition, predictive biomarkers for efficacy and toxicity are lacking. Industry-academy cooperation is urgently required to develop CAR-T therapy that is effective, safe, and affordable for patients in Korea.


Subject(s)
Humans , B-Lymphocytes , Biomarkers , Cell- and Tissue-Based Therapy , Korea , Lymphoma, B-Cell , Lymphoma, Large B-Cell, Diffuse , Organization and Administration , Receptors, Antigen , T-Lymphocytes , United States Food and Drug Administration
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