The biggest gap are those patients that progress after bispecific and CAR T. Even after CAR T, we know that bispecific, the progression of his survival is very short. This was a Eliza study showing a median PFS of only three months with glofitamab, so different strategies are needed. That’s where the new agents like the CELMoDs and the newer bispecifics like the surovatamig CD19, CD3 may have a role...
The biggest gap are those patients that progress after bispecific and CAR T. Even after CAR T, we know that bispecific, the progression of his survival is very short. This was a Eliza study showing a median PFS of only three months with glofitamab, so different strategies are needed. That’s where the new agents like the CELMoDs and the newer bispecifics like the surovatamig CD19, CD3 may have a role. Also, they’re in development in vivo CAR-T that although has not been tested in this setting, potentially can be associated with higher activity in the early lines of therapy or in patients that after frontline immunochemotherapy are MRD positive. Also, the tri-specifics and tetra-specifics are in development and we look forward to see the data to see if they will have any role in the treatment for these patients.
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