In the SUCCESSOR-2 study, patients were included that were relatively heavily pretreated. They had received a median of two prior lines of therapy and about a quarter of these patients had received four or more prior lines of therapy. Furthermore, all these patients were exposed and most of them refractory to both lenalidomide and anti-CD38. So in the context of this particular patient population, we saw a doubling of progression-free survival as compared to the control arm, carfilzomib and dexamethasone...
In the SUCCESSOR-2 study, patients were included that were relatively heavily pretreated. They had received a median of two prior lines of therapy and about a quarter of these patients had received four or more prior lines of therapy. Furthermore, all these patients were exposed and most of them refractory to both lenalidomide and anti-CD38. So in the context of this particular patient population, we saw a doubling of progression-free survival as compared to the control arm, carfilzomib and dexamethasone. I believe that these data are very encouraging. There are patients that could be treated with this regimen. This regimen can be given to outpatients. Lenalidomide is given orally. Carfilzomib is given intravenously every week. It could be given on an outpatient basis and even in small practice settings. So I believe that this is an important combination for the treatment of myeloma.
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