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An expert panel hosted by
Sequencing immune-based therapies in B-cell malignancies
with Ulric Jäger, Sagar Lonial, and Krina Patel
Saturday, June 15 | 18:00-19:30 CEST
Register nowThis independent education activity is sponsored by Bristol Myers Squibb. All content is developed independently by the faculty. Funders are allowed no direct influence on the content of this activity.
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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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