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EHA 2024 | Indirect comparison of elranatamab in MagnetisMM-3 versus real-world treatment regimens

Luciano Costa, MD, PhD, UAB School of Medicine, Birmingham, AL, discusses an indirect comparison of outcomes for patients with multiple myeloma (MM) treated with elranatamab in the MagnetisMM-3 trial (NCT04649359) versus real-world treatment regimens. The analysis indicates that elranatamab provides a greater frequency and longer duration of response in patients compared to other regimens, making it a potential option for triple-class exposed (TCE) patients. This interview took place at the 29th Congress of the European Hematology Association (EHA) in Madrid, Spain.

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Transcript

So we’re presenting at EHA an analysis that essentially took data from MagnetisMM-3, which is the main trial for elranatamab and compare with real-world data for different regimens that are commonly used in different parts of the world, acknowledging that practice varies from country to country based on drug availability, preferences and other things. And what we’ve seen consistently is when you take real-world patients who have a similar profile of the patients who participate in MagnetisMM-3 around different countries around the world in Europe and the US, you see that consistently there is a greater frequency of responses and longer duration of response that we see with elranatamab, when compared to kind of real-world multiplicity of regimens using throughout...

So we’re presenting at EHA an analysis that essentially took data from MagnetisMM-3, which is the main trial for elranatamab and compare with real-world data for different regimens that are commonly used in different parts of the world, acknowledging that practice varies from country to country based on drug availability, preferences and other things. And what we’ve seen consistently is when you take real-world patients who have a similar profile of the patients who participate in MagnetisMM-3 around different countries around the world in Europe and the US, you see that consistently there is a greater frequency of responses and longer duration of response that we see with elranatamab, when compared to kind of real-world multiplicity of regimens using throughout. So this further strengthens the case for elranatamab as an option for patients who have particularly triple-class exposed disease who are in need of further therapy, of this agent being superior to any combination that is commonly currently used that includes monoclonal antibodies, PIs, and IMiDs.

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