Most patients who progress or relapse after CAR-T would be considered for CD20xCD3 bispecific antibody therapies. These are highly effective treatments. We’ve seen long-term remission rates from long-term follow-up from the pivotal studies. In some patients, these treatments are actually considered alternative to CAR-T. We’ve now seen more and more real-world data coming through looking at bispecific outcomes including those who receive bispecifics post CAR-T and it looks like overall outcomes are slightly inferior to what we’ve seen in the pivotal studies, which was expected given the high-risk patient population in the real-world setting, but there doesn’t seem to be a significant impact on whether or not patients had prior CAR-T...
Most patients who progress or relapse after CAR-T would be considered for CD20xCD3 bispecific antibody therapies. These are highly effective treatments. We’ve seen long-term remission rates from long-term follow-up from the pivotal studies. In some patients, these treatments are actually considered alternative to CAR-T. We’ve now seen more and more real-world data coming through looking at bispecific outcomes including those who receive bispecifics post CAR-T and it looks like overall outcomes are slightly inferior to what we’ve seen in the pivotal studies, which was expected given the high-risk patient population in the real-world setting, but there doesn’t seem to be a significant impact on whether or not patients had prior CAR-T. But those who relapse very soon after CAR-T, those patients have poor outcomes but we really don’t know whether they would do any better with alternative treatments, I suspect they would. But these ultra high-risk patients, would do very poorly with whichever post-CAR-T treatment you would consider.
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