Well, that is a difficult question and could probably take quite a while to answer. The short version is that many doctors and academic centers, at least for certain subgroups, use MRD results to guide therapy. Probably the best example is in NPM1 mutant patients who, if they achieve MRD negativity after two cycles of chemotherapy, generally you’re thought not to require allogeneic stem cell transplant and consolidation, whereas the ones who are MRD positive might benefit from allogeneic stem cell transplant...
Well, that is a difficult question and could probably take quite a while to answer. The short version is that many doctors and academic centers, at least for certain subgroups, use MRD results to guide therapy. Probably the best example is in NPM1 mutant patients who, if they achieve MRD negativity after two cycles of chemotherapy, generally you’re thought not to require allogeneic stem cell transplant and consolidation, whereas the ones who are MRD positive might benefit from allogeneic stem cell transplant. I think that’s the most clear-cut use and maybe the most common use of MRD to guide post-remission therapy. There’s emerging data with a super-sensitive FLT3 assay that might guide the, if positive, before or after stem cell transplant, that might guide the use of gilteritinib in the post-transplant setting for FLT3 mutant patients. Otherwise, it’s a bit less clear-cut, although many studies are being done to try to evaluate the utility and potential surrogacy of MRD positivity to predict overall outcome for patients.
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