MAGNOLIA trial: zanubrutinib for MZL
Stephen Opat, FRACP, FRCPA, MBBS, Monash University, Melbourne, Australia, shares the findings of the Phase II MAGNOLIA trial (NCT03846427) evaluating the safety and efficacy of a next-generation Bruton’s tyrosine kinase inhibitor, zanubrutinib, in patients with relapsed/refractory (R/R) marginal zone lymphoma (MZL). After 10 months, zanubrutinib has been shown to be efficacious, with a 74% overall response rate (ORR) and rates expected to increase with longer follow-up. The clinical benefits seen with zanubrutinib use extended to various MZL subtypes including extranodal, nodal, and splenic. A favorable safety profile was observed, with the most common adverse event being neutropenia. Follow-up is ongoing to improve understanding of the durability of responses. This interview took place during the 62nd American Society of Hematology (ASH) Annual Meeting and Exposition, 2020.
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