
Opinion|Videos|October 25, 2024
Impact of SC Daratumumab
Key Takeaways
- FDA approval of daratumumab and hyaluronidase-fihj with VRd offers new treatment options for transplant-eligible multiple myeloma patients, potentially improving outcomes.
- The combination therapy's approval signifies a shift towards more comprehensive and effective treatment regimens in newly diagnosed multiple myeloma.
Panelists discuss how the FDA approval of daratumumab and hyaluronidase-fihj combined with VRd (bortezomib, lenalidomide, and dexamethasone) for induction and consolidation in transplant-eligible newly diagnosed multiple myeloma patients is changing treatment approaches while also considering how recent evidence suggesting reduced observation time for subcutaneous (SC) daratumumab administration may streamline patient care and improve treatment efficiency.
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Episodes in this series

Video content above is prompted by the following:
- With the new FDA approval of daratumumab and hyaluronidase-fihj in combination with VRd (bortezomib, lenalidomide, and dexamethasone) for induction and consolidation in transplant-eligible patients with newly diagnosed multiple myeloma, how does this impact treatment within this patient population?
- (Dr Adams) A recent pharmacy-led initiative showed that observation following subcutaneous administration of daratumumab may not be needed if the first injection is tolerated. How does this change patient monitoring procedures by the care team?
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An MRD-guided strategy incorporating teclistamab-daratumumab intensification produced deep responses in newly diagnosed high-risk multiple myeloma, although infections affected more than three-quarters of treated patients.

