I think the data presented at ASH 2024 again confirm the efficacy of luspatercept as a first-line therapy in transfusion-dependent patients with lower-risk MDS, irrespective of the molecular status. So responses are seen actually across all subtypes of MDS with, of course, patients with the ring sideroblastic phenotype having a higher response rate compared to patients without this ring sideroblastic positive phenotype...
I think the data presented at ASH 2024 again confirm the efficacy of luspatercept as a first-line therapy in transfusion-dependent patients with lower-risk MDS, irrespective of the molecular status. So responses are seen actually across all subtypes of MDS with, of course, patients with the ring sideroblastic phenotype having a higher response rate compared to patients without this ring sideroblastic positive phenotype. So I think this still holds, but also a substantial amount of patients had a durable response exceeding a time period of one year. I think that’s great. And this was also significantly higher compared to the current standard of care, which is EPO-ESA-based therapy. In general, the quality of life did not get worse during the treatment course, there were some early signals of more fatigue, but the majority of those patients actually improved significantly with continuation of therapy or sometimes dose reductions. I think the take home message from all of those presentations is a confirmation of the high efficacy, the durability, and also the safety with regards to quality of life.
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