{"version":"1.0","type":"rich","provider_name":"Acast","provider_url":"https://acast.com","height":250,"width":700,"html":"<iframe src=\"https://embed.acast.com/$/5ebe8cc563e3d811bbd2c9d8/6aa9473afca3d5c77b5c7ea8?\" frameBorder=\"0\" width=\"700\" height=\"250\"></iframe>","title":" Belantamab mafodotin in RRMM: Latest updates and practical considerations","description":"<p>The Multiple Myeloma Hub spoke with Christoph Renner, University of Basel, Basel, CH. We asked about the use of belantamab mafodotin-based combination therapy for relapsed/refractory multiple myeloma (RRMM). </p><p> </p><p>During this interview, Renner provides an overview of pivotal clinical data from the DREAMM-7 and DREAMM-8 trials that supported regulatory approvals of belantamab mafodotin-based combinations in RRMM and outlines practical considerations for their use in clinical practice. Renner discusses patient selection and treatment sequencing alongside other BCMA-directed therapies, as well as the monitoring and management of associated ocular toxicities. Renner draws on his experience in Switzerland and highlights the importance of multidisciplinary collaboration, particularly between hematology and ophthalmology, to support the management of ocular toxicities and inform treatment decisions. </p><p> </p><p>Intended for healthcare professionals. This educational resource is independently supported by GSK. All content is developed by SES in collaboration with an expert steering committee. Funders are allowed no influence.</p>","author_name":"Scientific Education Support"}