So in Burkitt lymphoma, we’ve had a few studies that discussed frontline, and what we now know is, of course, the addition of rituximab makes a difference, but it’s not clear what the optimal backbone is. And so I did discuss some of that, showing that the CODOX-M/IVAC compared to the R-EPOCH, may be more toxic, but it’s not clear that it’s a better regimen. And we also looked at relapsed/refractory data, which is very abysmal...
So in Burkitt lymphoma, we’ve had a few studies that discussed frontline, and what we now know is, of course, the addition of rituximab makes a difference, but it’s not clear what the optimal backbone is. And so I did discuss some of that, showing that the CODOX-M/IVAC compared to the R-EPOCH, may be more toxic, but it’s not clear that it’s a better regimen. And we also looked at relapsed/refractory data, which is very abysmal. And we just published our series from MSK, which is similar to others, showing that almost no one survives if they have a relapse. So what we want to do is make a better improvement in the frontline setting. And I’m very excited because our study that incorporates adding a bispecific to the highest risk patients was sent to CTA for approval on Friday. So that protocol is now completely written and we’re hoping to activate it by the fourth quarter of 2025.
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