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Published byLenard Floyd Modified over 6 years ago
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Harnessing the Immune System: Mechanism of Action of Immunotherapies in B-Cell Malignancies
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Learning Goals
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Immunotherapies in B-Cell Malignancies
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Available Immunotherapies
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OS in MM
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Poor Outcome in High-Risk Myeloma
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Immunotherapy Potential for Success Without a Targetable Molecular Mutation
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Available Immunotherapies
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Monoclonal Antibodies Approved for MM
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Elotuzumab and Daratumumab
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Daratumumab
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Elotuzumab
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Daratumumab Potential MOA
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Daratumumab Monotherapy Phase 2 Study, ≥ 3 Lines of Prior Therapy
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Daratumumab in Combination
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CASTOR Study Daratumumab + Bor/Dex vs Bor/Dex
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CASTOR Study Efficacy Endpoints and IRRs
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POLLUX Daratumumab + Len/Dex vs Len/Dex
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Elotuzumab MOA
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ELOQUENT-2 Elotuzumab + Len/Dex vs Len/Dex
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ELOQUENT-2
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Therapies in Development Antibodies
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Antibody Drug Conjugates
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Brentuximab Vedotin
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AETHERA Brentuximab Vedotin as Consolidation Therapy After ASCT in Patients With HL
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Other ADCs in Development for MM
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T-Cell Receptors Activating and Inhibitory
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Checkpoint Inhibitors in HL
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Checkpoint Inhibitors in MM
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Structure of Chimeric Antigen Receptors
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Clinical Trials With CAR-T Cells in MM
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CAR-T Cell Therapy
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Cytokine Release Syndrome (CRS)
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Response to Tocilizumab in 2 Patients
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Bispecific T-Cell Engagers
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Patient-Specific Dendritic Cell/MM Cell Fusion Vaccines Postautologous Transplant
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Response Rates After Vaccination
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Future of Immunotherapeutic Strategies in B-Cell Malignancies
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Conclusions
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Abbreviations
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Abbreviations (cont)
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Abbreviations (cont)
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Abbreviations (cont)
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