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Efficacy and safety of brexucabtagene autoleucel in patients with R/R MCL: a real-world analysis
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The Lymphoma Hub is pleased to present a visual abstract summarizing key safety and efficacy outcomes from a recent retrospective study investigating brexucabtagene autoleucel, an autologous CD19-directed chimeric antigen receptor T-cell therapy, as standard of care practice in patients with relapsed/refractory mantle cell lymphoma. In 2020, the U.S. Food and Drug Administration (FDA) approved brexucabtagene autoleucel for the treatment of relapsed/refractory mantle cell lymphoma; this approval was based on results of the phase II ZUMA-2 trial (NCT02601313), recently reported on the Lymphoma Hub.
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