Yeah, so marginal zone lymphoma is often a disease where most of our therapies are inferred from trials in follicular lymphoma. So to really have data specific to that population of patients and in a specific scenario after prior covalent BTK inhibitor, I think, really is unique. And so for me, personally, I think that the strength of that data is that it is really focused on marginal zone lymphoma...
Yeah, so marginal zone lymphoma is often a disease where most of our therapies are inferred from trials in follicular lymphoma. So to really have data specific to that population of patients and in a specific scenario after prior covalent BTK inhibitor, I think, really is unique. And so for me, personally, I think that the strength of that data is that it is really focused on marginal zone lymphoma. And so my own sequencing approach really is after a covalent BTK inhibitor, which I use quite commonly in marginal zone lymphoma, I think the data for pirtobrutinib is the strongest we have. And certainly we can see now we have CAR T-cells available as well in marginal zone lymphoma. But the population of patients enrolled in those trials is a little bit different. So I think for a patient who’s already had covalent BTK inhibitor, the strongest data we have really comes from that BRUIN experience.
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