This is another activity of us at the Harmony Alliance Foundation. We are following also the other risk factors that are relevant to AML because although genetics at initial diagnosis, what we have been focusing on in my abstract, is a hallmark attributing to about 63% of the factors that are relevant for prognosis. It’s modified with other factors, including age and also other factors such as treatments...
This is another activity of us at the Harmony Alliance Foundation. We are following also the other risk factors that are relevant to AML because although genetics at initial diagnosis, what we have been focusing on in my abstract, is a hallmark attributing to about 63% of the factors that are relevant for prognosis. It’s modified with other factors, including age and also other factors such as treatments. But the MRD, so the minimal residual and measurable residual disease, are adding value and they are refining risk for those patients after the treatments because the persistence of MRD is a risk factor, an independent risk factor. More importantly, and this is what my colleague has been focusing on, this is a factor that really can be utilized as a surrogate parameter because it becomes positive earlier. And this has impacts, of course, to clinical trials because clinical trials usually wait for the signals which are mortality or relapse signals. But if you can detect them, anticipate them, you can accelerate the treatment, and you can intervene earlier when it’s better to cure patients, for example, with an allogeneic transplantation. And the surrogacy of the MRD has been investigated previously, but not in that scale, and he was able to merge data for 1,800 patients to really investigate this diverse impact of the MRD. So good updates, hopefully also for the patients.
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