Approval of brexucabtagene autoleucel for adults with relapsed and refractory acute lymphocytic leukemia
Noelle V. Frey
Abstract
In October 2021, brexucabtagene autoleucel became the first anti-CD19 chimeric antigen receptor T-cell product to receive approval from the Food and Drug Administration to treat adults with relapsed and refractory B-cell acute lymphoblastic leukemia. The approval is based on results from the Zuma-3 trial and significantly widens treatment options for this patient population. In this article, we review outcomes from this study and its implications.
Topics & Concepts
Chimeric antigen receptorMedicineRefractory (planetary science)Acute lymphocytic leukemiaFood and drug administrationInternal medicineLeukemiaPopulationOncologyImmunologyLymphoblastic LeukemiaPharmacologyCancerImmunotherapyBiologyAstrobiologyEnvironmental healthCAR-T cell therapy research