I would say that, you know, there’s been quite a lot of studies showing that if you start treatments, even with erythropoiesis-stimulating agents, and there is another more novel agent, luspatercept, which is also a TGF-β modulator, which is approved in some countries for use. If you start treatment early in the disease course, we tend to get better and longer responses. So I think when patients present with myelodysplasia, if they have symptomatic anemia, it is probably advisable if you have access to start treatment a bit earlier...
I would say that, you know, there’s been quite a lot of studies showing that if you start treatments, even with erythropoiesis-stimulating agents, and there is another more novel agent, luspatercept, which is also a TGF-β modulator, which is approved in some countries for use. If you start treatment early in the disease course, we tend to get better and longer responses. So I think when patients present with myelodysplasia, if they have symptomatic anemia, it is probably advisable if you have access to start treatment a bit earlier. And if they become transfusion dependent, one has to watch the iron stores to make sure that they don’t get iron overloaded otherwise we need to start them on iron chelators because that can also impact their overall outcome.
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