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Korean Journal of Medicine ; : 152-158, 2019.
Artículo en Coreano | WPRIM | ID: wpr-759927

RESUMEN

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.


Asunto(s)
Humanos , Linfocitos B , Biomarcadores , Tratamiento Basado en Trasplante de Células y Tejidos , Corea (Geográfico) , Linfoma de Células B , Linfoma de Células B Grandes Difuso , Organización y Administración , Receptores de Antígenos , Linfocitos T , United States Food and Drug Administration
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