It’s very exciting that the classification and reclassification of these diseases seems to have plateaued. I think we’ve had a lot more concrete diagnostic criteria that have lasted across multiple diagnostic reclassification models. So I think we probably have a better understanding and definition of these diseases to start with. I think even better, we’re starting to have a better molecular definition of these diseases...
It’s very exciting that the classification and reclassification of these diseases seems to have plateaued. I think we’ve had a lot more concrete diagnostic criteria that have lasted across multiple diagnostic reclassification models. So I think we probably have a better understanding and definition of these diseases to start with. I think even better, we’re starting to have a better molecular definition of these diseases. I think we’re able to define these diseases by factual pathway mutations that define their behavior. And that our therapy is now being driven by biological considerations, not purely morphologic and clinical features. So I think that has been able to allow us to empower us to be able to design better studies that are biology-driven, not just morphology-driven or based on clinical judgment. So that is helpful, and it does feed into the biology and the rationale for that. It is an uphill task to design prospective studies in patients with these diseases. It is even more challenging to design randomized studies in these patients. But again, that has not stopped us, and hopefully we will have even more prospective data.
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