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|Videos|February 14, 2022

ASH 2021: Updates in the Chronic Lymphocytic Leukemia Treatment Landscape

Author(s)Matthew S. Davids, MD, MMSc, Dana-Farber Cancer Institute, Jae Park, MD, Memorial Sloan Kettering Cancer Center, Elias J. Jabbour, MD, MD Anderson

Following the ASH 2021 annual meeting, expert hematologist/oncologists discuss updates in chronic lymphocytic leukemia.

Episodes in this series

Expert on Leukemia

EP. 1 ASH 2021: Novel Therapy in Acute Lymphocytic Leukemia

Expert on Leukemia

EP. 2 ASH 2021: Key Data in Chronic Myeloid Leukemia

Expert on Leukemia

EP. 3 ASH 2021: Updates in the Chronic Lymphocytic Leukemia Treatment Landscape

Data from the following clinical trials are discussed:

3721: Characterization of Bruton tyrosine kinase inhibitor (BTKi)-related adverse events in a head-to-head trial acalabrutinib versus ibrutinib in previously chronic lymphocytic leukemia (CLL)
68: First-line treatment with ibrutinib (Ibr) plus venetoclax (Ven) for chronic lymphocytic leukemia (CLL): 2-year post-randomization disease-free survival (DFS) results from the minimal residual disease (MRD) cohort of the phase 2 Captivate study
396: SEQUOIA: Results of a phase 3 randomized study of zanubrutinib versus bendamustine + rituximab (BR) in patients with treatment-naïve (TN) chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL)
67: Zanubrutinib in combination with venetoclax for patients with treatment-naïve (TN) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) with del(17p): early results from arm D of the SEQUOIA (BGB-311-304) trial
1410: Phase 2 study of zanubrutinib in BTK inhibitor-intolerant patients (Pts) with relapsed/refractory B-cell malignancies
395: A phase 2 study evaluating the addition of ublituximab and umbralisib (U2) to ibrutinib in patients with chronic lymphocytic leukemia (CLL): a minimal residual disease (MRD)-driven, time-limited approach
391: Pirtobrutinib, a next generation, highly selective, non-covalent BTK inhibitor in previously treated CLL/SLL: updated results from the phase 1/2 BRUIN study

Supported in part by Takeda Oncology. Content developed independently by Onclive®.

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